US20030087407A1 - Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits - Google Patents
Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits Download PDFInfo
- Publication number
- US20030087407A1 US20030087407A1 US10/235,483 US23548302A US2003087407A1 US 20030087407 A1 US20030087407 A1 US 20030087407A1 US 23548302 A US23548302 A US 23548302A US 2003087407 A1 US2003087407 A1 US 2003087407A1
- Authority
- US
- United States
- Prior art keywords
- seq
- amyloid
- peptide
- amino acid
- sheet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 108090000765 processed proteins & peptides Proteins 0.000 title claims abstract description 316
- 102000004196 processed proteins & peptides Human genes 0.000 title claims abstract description 95
- 230000002159 abnormal effect Effects 0.000 title claims abstract description 24
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract description 55
- 201000010099 disease Diseases 0.000 title abstract description 31
- 208000035475 disorder Diseases 0.000 title abstract description 24
- 238000011282 treatment Methods 0.000 title description 15
- 230000012846 protein folding Effects 0.000 title description 10
- 239000008194 pharmaceutical composition Substances 0.000 title description 7
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 63
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 44
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 38
- 239000002243 precursor Substances 0.000 claims abstract description 35
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 28
- 125000000539 amino acid group Chemical group 0.000 claims abstract description 27
- 230000001575 pathological effect Effects 0.000 claims abstract description 22
- 150000001413 amino acids Chemical class 0.000 claims description 176
- 230000002401 inhibitory effect Effects 0.000 claims description 50
- 230000000903 blocking effect Effects 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 7
- 125000001165 hydrophobic group Chemical group 0.000 claims description 4
- 150000008574 D-amino acids Chemical group 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 208000024827 Alzheimer disease Diseases 0.000 abstract description 30
- 238000000034 method Methods 0.000 abstract description 20
- 102000029797 Prion Human genes 0.000 abstract description 18
- 108091000054 Prion Proteins 0.000 abstract description 18
- 208000014644 Brain disease Diseases 0.000 abstract description 2
- 208000032274 Encephalopathy Diseases 0.000 abstract description 2
- 229940024606 amino acid Drugs 0.000 description 179
- 235000001014 amino acid Nutrition 0.000 description 178
- 230000003941 amyloidogenesis Effects 0.000 description 44
- 239000003112 inhibitor Substances 0.000 description 34
- 235000018102 proteins Nutrition 0.000 description 32
- 102100021277 Beta-secretase 2 Human genes 0.000 description 28
- 238000011534 incubation Methods 0.000 description 27
- 230000035557 fibrillogenesis Effects 0.000 description 25
- 101710150190 Beta-secretase 2 Proteins 0.000 description 22
- 230000000694 effects Effects 0.000 description 21
- 239000012634 fragment Substances 0.000 description 20
- 230000005764 inhibitory process Effects 0.000 description 17
- 208000037259 Amyloid Plaque Diseases 0.000 description 16
- 102000054727 Serum Amyloid A Human genes 0.000 description 16
- 108010064397 amyloid beta-protein (1-40) Proteins 0.000 description 16
- 108010064539 amyloid beta-protein (1-42) Proteins 0.000 description 16
- 102000009091 Amyloidogenic Proteins Human genes 0.000 description 15
- 108010048112 Amyloidogenic Proteins Proteins 0.000 description 15
- 108700028909 Serum Amyloid A Proteins 0.000 description 15
- 206010002022 amyloidosis Diseases 0.000 description 15
- 238000000338 in vitro Methods 0.000 description 15
- 101710138751 Major prion protein Proteins 0.000 description 14
- 102100025818 Major prion protein Human genes 0.000 description 14
- 102000001049 Amyloid Human genes 0.000 description 13
- 108010094108 Amyloid Proteins 0.000 description 13
- 108010008685 alanyl-glutamyl-aspartic acid Proteins 0.000 description 13
- 230000003993 interaction Effects 0.000 description 13
- OBMZMSLWNNWEJA-XNCRXQDQSA-N C1=CC=2C(C[C@@H]3NC(=O)[C@@H](NC(=O)[C@H](NC(=O)N(CC#CCN(CCCC[C@H](NC(=O)[C@@H](CC4=CC=CC=C4)NC3=O)C(=O)N)CC=C)NC(=O)[C@@H](N)C)CC3=CNC4=C3C=CC=C4)C)=CNC=2C=C1 Chemical compound C1=CC=2C(C[C@@H]3NC(=O)[C@@H](NC(=O)[C@H](NC(=O)N(CC#CCN(CCCC[C@H](NC(=O)[C@@H](CC4=CC=CC=C4)NC3=O)C(=O)N)CC=C)NC(=O)[C@@H](N)C)CC3=CNC4=C3C=CC=C4)C)=CNC=2C=C1 OBMZMSLWNNWEJA-XNCRXQDQSA-N 0.000 description 12
- 241001465754 Metazoa Species 0.000 description 12
- 101710176384 Peptide 1 Proteins 0.000 description 12
- 238000004090 dissolution Methods 0.000 description 12
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 12
- 108010067770 Endopeptidase K Proteins 0.000 description 11
- 230000000875 corresponding effect Effects 0.000 description 11
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 10
- 238000007421 fluorometric assay Methods 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- JKJSIYKSGIDHPM-WBAXXEDZSA-N Phe-Phe-Ala Chemical compound C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](N)Cc1ccccc1)C(O)=O JKJSIYKSGIDHPM-WBAXXEDZSA-N 0.000 description 9
- 125000003275 alpha amino acid group Chemical group 0.000 description 9
- 108010000737 amyloid enhancing factor Proteins 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000001727 in vivo Methods 0.000 description 9
- 108010073025 phenylalanylphenylalanine Proteins 0.000 description 9
- 208000003736 Gerstmann-Straussler-Scheinker Disease Diseases 0.000 description 8
- FKXCBKCOSVIGCT-AVGNSLFASA-N Gln-Lys-Leu Chemical compound [H]N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(O)=O FKXCBKCOSVIGCT-AVGNSLFASA-N 0.000 description 8
- DHINLYMWMXQGMQ-IHRRRGAJSA-N Val-His-His Chemical compound C([C@H](NC(=O)[C@@H](N)C(C)C)C(=O)N[C@@H](CC=1NC=NC=1)C(O)=O)C1=CN=CN1 DHINLYMWMXQGMQ-IHRRRGAJSA-N 0.000 description 8
- 108010087924 alanylproline Proteins 0.000 description 8
- 210000004027 cell Anatomy 0.000 description 8
- 238000002983 circular dichroism Methods 0.000 description 8
- 238000013461 design Methods 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 8
- 238000002347 injection Methods 0.000 description 8
- 239000007924 injection Substances 0.000 description 8
- 235000013930 proline Nutrition 0.000 description 8
- JADVWWSKYZXRGX-UHFFFAOYSA-M thioflavine T Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C1=[N+](C)C2=CC=C(C)C=C2S1 JADVWWSKYZXRGX-UHFFFAOYSA-M 0.000 description 8
- KXEVYGKATAMXJJ-ACZMJKKPSA-N Ala-Glu-Asp Chemical compound C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O KXEVYGKATAMXJJ-ACZMJKKPSA-N 0.000 description 7
- 101710137189 Amyloid-beta A4 protein Proteins 0.000 description 7
- 102100022704 Amyloid-beta precursor protein Human genes 0.000 description 7
- 101710151993 Amyloid-beta precursor protein Proteins 0.000 description 7
- 108010087049 alanyl-alanyl-prolyl-valine Proteins 0.000 description 7
- 230000003942 amyloidogenic effect Effects 0.000 description 7
- 230000008499 blood brain barrier function Effects 0.000 description 7
- 210000001218 blood-brain barrier Anatomy 0.000 description 7
- -1 cationic amino acid Chemical group 0.000 description 7
- 238000001493 electron microscopy Methods 0.000 description 7
- WATXSTJXNBOHKD-LAEOZQHASA-N Glu-Asp-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O WATXSTJXNBOHKD-LAEOZQHASA-N 0.000 description 6
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 6
- 229920002971 Heparan sulfate Polymers 0.000 description 6
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 6
- 208000024777 Prion disease Diseases 0.000 description 6
- DZHSAHHDTRWUTF-SIQRNXPUSA-N amyloid-beta polypeptide 42 Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O)[C@@H](C)CC)C(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)C1=CC=CC=C1 DZHSAHHDTRWUTF-SIQRNXPUSA-N 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 230000008876 conformational transition Effects 0.000 description 6
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 230000035772 mutation Effects 0.000 description 6
- 239000002953 phosphate buffered saline Substances 0.000 description 6
- 208000008864 scrapie Diseases 0.000 description 6
- 229910001961 silver nitrate Inorganic materials 0.000 description 6
- 210000000952 spleen Anatomy 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 108090000197 Clusterin Proteins 0.000 description 5
- 102000003780 Clusterin Human genes 0.000 description 5
- 208000020406 Creutzfeldt Jacob disease Diseases 0.000 description 5
- 208000003407 Creutzfeldt-Jakob Syndrome Diseases 0.000 description 5
- 208000010859 Creutzfeldt-Jakob disease Diseases 0.000 description 5
- CZVQSYNVUHAILZ-UWVGGRQHSA-N His-Lys Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H](N)CC1=CN=CN1 CZVQSYNVUHAILZ-UWVGGRQHSA-N 0.000 description 5
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 5
- HVAUKHLDSDDROB-KKUMJFAQSA-N Lys-Lys-Leu Chemical compound [H]N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(O)=O HVAUKHLDSDDROB-KKUMJFAQSA-N 0.000 description 5
- 241000699670 Mus sp. Species 0.000 description 5
- 108091005804 Peptidases Proteins 0.000 description 5
- BUEIYHBJHCDAMI-UFYCRDLUSA-N Pro-Phe-Phe Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O BUEIYHBJHCDAMI-UFYCRDLUSA-N 0.000 description 5
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 5
- 239000004365 Protease Substances 0.000 description 5
- 108010029485 Protein Isoforms Proteins 0.000 description 5
- 102000001708 Protein Isoforms Human genes 0.000 description 5
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 5
- 239000007983 Tris buffer Substances 0.000 description 5
- 230000002776 aggregation Effects 0.000 description 5
- 238000004220 aggregation Methods 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 210000004556 brain Anatomy 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- 108010054813 diprotin B Proteins 0.000 description 5
- 231100000673 dose–response relationship Toxicity 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 230000001537 neural effect Effects 0.000 description 5
- 125000001500 prolyl group Chemical group [H]N1C([H])(C(=O)[*])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 5
- 235000019419 proteases Nutrition 0.000 description 5
- SBGXWWCLHIOABR-UHFFFAOYSA-N Ala Ala Gly Ala Chemical compound CC(N)C(=O)NC(C)C(=O)NCC(=O)NC(C)C(O)=O SBGXWWCLHIOABR-UHFFFAOYSA-N 0.000 description 4
- OTCJMMRQBVDQRK-DCAQKATOSA-N Arg-Asp-Leu Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(O)=O OTCJMMRQBVDQRK-DCAQKATOSA-N 0.000 description 4
- KRXIWXCXOARFNT-ZLUOBGJFSA-N Asp-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O KRXIWXCXOARFNT-ZLUOBGJFSA-N 0.000 description 4
- 241000699800 Cricetinae Species 0.000 description 4
- 201000010374 Down Syndrome Diseases 0.000 description 4
- 102000004878 Gelsolin Human genes 0.000 description 4
- 108090001064 Gelsolin Proteins 0.000 description 4
- 241000282412 Homo Species 0.000 description 4
- 206010061218 Inflammation Diseases 0.000 description 4
- 101100440173 Mus musculus Clu gene Proteins 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- DZZCICYRSZASNF-FXQIFTODSA-N Pro-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1 DZZCICYRSZASNF-FXQIFTODSA-N 0.000 description 4
- 206010044688 Trisomy 21 Diseases 0.000 description 4
- VREFGVBLTWBCJP-UHFFFAOYSA-N alprazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1 VREFGVBLTWBCJP-UHFFFAOYSA-N 0.000 description 4
- 210000004899 c-terminal region Anatomy 0.000 description 4
- 230000001413 cellular effect Effects 0.000 description 4
- 238000001142 circular dichroism spectrum Methods 0.000 description 4
- 230000001419 dependent effect Effects 0.000 description 4
- 238000002189 fluorescence spectrum Methods 0.000 description 4
- VPZXBVLAVMBEQI-UHFFFAOYSA-N glycyl-DL-alpha-alanine Natural products OC(=O)C(C)NC(=O)CN VPZXBVLAVMBEQI-UHFFFAOYSA-N 0.000 description 4
- 230000004054 inflammatory process Effects 0.000 description 4
- 108010057821 leucylproline Proteins 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 208000015122 neurodegenerative disease Diseases 0.000 description 4
- 230000008506 pathogenesis Effects 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 108010053725 prolylvaline Proteins 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- XPZWWTIIKSODDO-MBNDGZRNSA-N 148439-49-0 Chemical compound OC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)CNC(=O)[C@H](C(C)C)NC(=O)[C@H](C(C)C)NC(=O)[C@H](C)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCCN)[C@@H](C)O)CC1=CN=CN1 XPZWWTIIKSODDO-MBNDGZRNSA-N 0.000 description 3
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 3
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 description 3
- 208000023769 AA amyloidosis Diseases 0.000 description 3
- 102100029470 Apolipoprotein E Human genes 0.000 description 3
- 101710095339 Apolipoprotein E Proteins 0.000 description 3
- RWCLSUOSKWTXLA-FXQIFTODSA-N Arg-Asp-Ala Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(O)=O RWCLSUOSKWTXLA-FXQIFTODSA-N 0.000 description 3
- XPGVTUBABLRGHY-BIIVOSGPSA-N Asp-Ala-Pro Chemical compound C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CC(=O)O)N XPGVTUBABLRGHY-BIIVOSGPSA-N 0.000 description 3
- 101100505161 Caenorhabditis elegans mel-32 gene Proteins 0.000 description 3
- 102100037907 High mobility group protein B1 Human genes 0.000 description 3
- 101710168537 High mobility group protein B1 Proteins 0.000 description 3
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 3
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 3
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 3
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 3
- XXXXOVFBXRERQL-ULQDDVLXSA-N Leu-Pro-Phe Chemical compound CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 XXXXOVFBXRERQL-ULQDDVLXSA-N 0.000 description 3
- GAELMDJMQDUDLJ-BQBZGAKWSA-N Met-Ala-Gly Chemical compound CSCC[C@H](N)C(=O)N[C@@H](C)C(=O)NCC(O)=O GAELMDJMQDUDLJ-BQBZGAKWSA-N 0.000 description 3
- UFOWQBYMUILSRK-IHRRRGAJSA-N Met-Lys-His Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(O)=O)CC1=CNC=N1 UFOWQBYMUILSRK-IHRRRGAJSA-N 0.000 description 3
- 108010033276 Peptide Fragments Proteins 0.000 description 3
- 102000007079 Peptide Fragments Human genes 0.000 description 3
- KIZQGKLMXKGDIV-BQBZGAKWSA-N Pro-Ala-Gly Chemical compound OC(=O)CNC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1 KIZQGKLMXKGDIV-BQBZGAKWSA-N 0.000 description 3
- WQUURFHRUAZQHU-VGWMRTNUSA-N Pro-Val-Val-Pro Chemical compound CC(C)[C@@H](C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)O)NC(=O)[C@@H]2CCCN2 WQUURFHRUAZQHU-VGWMRTNUSA-N 0.000 description 3
- 108010067787 Proteoglycans Proteins 0.000 description 3
- 102000016611 Proteoglycans Human genes 0.000 description 3
- 238000010171 animal model Methods 0.000 description 3
- 210000001124 body fluid Anatomy 0.000 description 3
- 239000010839 body fluid Substances 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 230000007541 cellular toxicity Effects 0.000 description 3
- 210000000349 chromosome Anatomy 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000000635 electron micrograph Methods 0.000 description 3
- 238000001962 electrophoresis Methods 0.000 description 3
- 230000005284 excitation Effects 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 108010050848 glycylleucine Proteins 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 238000010172 mouse model Methods 0.000 description 3
- 230000004770 neurodegeneration Effects 0.000 description 3
- 210000002569 neuron Anatomy 0.000 description 3
- 238000007911 parenteral administration Methods 0.000 description 3
- 238000011533 pre-incubation Methods 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 150000003148 prolines Chemical class 0.000 description 3
- 230000017854 proteolysis Effects 0.000 description 3
- 230000002797 proteolythic effect Effects 0.000 description 3
- 238000010791 quenching Methods 0.000 description 3
- 230000000171 quenching effect Effects 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 3
- 239000003981 vehicle Substances 0.000 description 3
- SICITCLFXRGKJW-IIZANFQQSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-2,6-diaminohexanoyl]amino]-4-methylpentanoyl]amino]-3-methylbutanoyl]amino]-3-phenylpropanoyl]amino]-3-phenylpropanoic acid Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCCN)CC(C)C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 SICITCLFXRGKJW-IIZANFQQSA-N 0.000 description 2
- 208000023761 AL amyloidosis Diseases 0.000 description 2
- 101150037123 APOE gene Proteins 0.000 description 2
- CXRCVCURMBFFOL-FXQIFTODSA-N Ala-Ala-Pro Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(O)=O CXRCVCURMBFFOL-FXQIFTODSA-N 0.000 description 2
- NLYYHIKRBRMAJV-AEJSXWLSSA-N Ala-Val-Pro Chemical compound C[C@@H](C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)O)N NLYYHIKRBRMAJV-AEJSXWLSSA-N 0.000 description 2
- 102100022524 Alpha-1-antichymotrypsin Human genes 0.000 description 2
- 208000000044 Amnesia Diseases 0.000 description 2
- 108010090849 Amyloid beta-Peptides Proteins 0.000 description 2
- 102000013455 Amyloid beta-Peptides Human genes 0.000 description 2
- 102000007592 Apolipoproteins Human genes 0.000 description 2
- 108010071619 Apolipoproteins Proteins 0.000 description 2
- JPAWCMXVNZPJLO-IHRRRGAJSA-N Arg-Ser-Phe Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O JPAWCMXVNZPJLO-IHRRRGAJSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 102000005367 Carboxypeptidases Human genes 0.000 description 2
- 108010006303 Carboxypeptidases Proteins 0.000 description 2
- 108020004414 DNA Proteins 0.000 description 2
- 101100216294 Danio rerio apoeb gene Proteins 0.000 description 2
- 206010012289 Dementia Diseases 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 2
- DBUNZBWUWCIELX-JHEQGTHGSA-N Gly-Thr-Glu Chemical compound [H]NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(O)=O)C(O)=O DBUNZBWUWCIELX-JHEQGTHGSA-N 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- 102000015779 HDL Lipoproteins Human genes 0.000 description 2
- 108010010234 HDL Lipoproteins Proteins 0.000 description 2
- 102000003855 L-lactate dehydrogenase Human genes 0.000 description 2
- 108700023483 L-lactate dehydrogenases Proteins 0.000 description 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 2
- YUTNOGOMBNYPFH-XUXIUFHCSA-N Leu-Pro-Ile Chemical compound [H]N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H]([C@@H](C)CC)C(O)=O YUTNOGOMBNYPFH-XUXIUFHCSA-N 0.000 description 2
- 208000026139 Memory disease Diseases 0.000 description 2
- YHBHDYYHOUAKLR-AVGNSLFASA-N Met-Met-His Chemical compound CSCC[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)N YHBHDYYHOUAKLR-AVGNSLFASA-N 0.000 description 2
- 241000699666 Mus <mouse, genus> Species 0.000 description 2
- 108090000189 Neuropeptides Proteins 0.000 description 2
- 241000282943 Odocoileus Species 0.000 description 2
- 241001494479 Pecora Species 0.000 description 2
- WKLMCMXFMQEKCX-SLFFLAALSA-N Phe-Phe-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC3=CC=CC=C3)N)C(=O)O WKLMCMXFMQEKCX-SLFFLAALSA-N 0.000 description 2
- GLJZDMZJHFXJQG-BZSNNMDCSA-N Phe-Ser-Phe Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O GLJZDMZJHFXJQG-BZSNNMDCSA-N 0.000 description 2
- ZMLRZBWCXPQADC-TUAOUCFPSA-N Pro-Val-Pro Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@@H]2CCCN2 ZMLRZBWCXPQADC-TUAOUCFPSA-N 0.000 description 2
- FHJQROWZEJFZPO-SRVKXCTJSA-N Pro-Val-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H]1CCCN1 FHJQROWZEJFZPO-SRVKXCTJSA-N 0.000 description 2
- 108010076504 Protein Sorting Signals Proteins 0.000 description 2
- 206010039811 Secondary amyloidosis Diseases 0.000 description 2
- NRCJWSGXMAPYQX-LPEHRKFASA-N Ser-Arg-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CO)N)C(=O)O NRCJWSGXMAPYQX-LPEHRKFASA-N 0.000 description 2
- UOLGINIHBRIECN-FXQIFTODSA-N Ser-Glu-Glu Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(O)=O UOLGINIHBRIECN-FXQIFTODSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- COQLPRJCUIATTQ-UHFFFAOYSA-N Uranyl acetate Chemical compound O.O.O=[U]=O.CC(O)=O.CC(O)=O COQLPRJCUIATTQ-UHFFFAOYSA-N 0.000 description 2
- LAYSXAOGWHKNED-XPUUQOCRSA-N Val-Gly-Ser Chemical compound CC(C)[C@H](N)C(=O)NCC(=O)N[C@@H](CO)C(O)=O LAYSXAOGWHKNED-XPUUQOCRSA-N 0.000 description 2
- XBRMBDFYOFARST-AVGNSLFASA-N Val-His-Val Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](C(C)C)C(=O)O)N XBRMBDFYOFARST-AVGNSLFASA-N 0.000 description 2
- BCBFMJYTNKDALA-UFYCRDLUSA-N Val-Phe-Phe Chemical compound N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O BCBFMJYTNKDALA-UFYCRDLUSA-N 0.000 description 2
- VCIYTVOBLZHFSC-XHSDSOJGSA-N Val-Phe-Pro Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N2CCC[C@@H]2C(=O)O)N VCIYTVOBLZHFSC-XHSDSOJGSA-N 0.000 description 2
- NHXZRXLFOBFMDM-AVGNSLFASA-N Val-Pro-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)C(C)C NHXZRXLFOBFMDM-AVGNSLFASA-N 0.000 description 2
- QIVPZSWBBHRNBA-JYJNAYRXSA-N Val-Pro-Phe Chemical compound CC(C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(O)=O QIVPZSWBBHRNBA-JYJNAYRXSA-N 0.000 description 2
- AEFJNECXZCODJM-UWVGGRQHSA-N Val-Val-Gly Chemical compound CC(C)[C@H]([NH3+])C(=O)N[C@@H](C(C)C)C(=O)NCC([O-])=O AEFJNECXZCODJM-UWVGGRQHSA-N 0.000 description 2
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 2
- 208000018756 Variant Creutzfeldt-Jakob disease Diseases 0.000 description 2
- 230000001154 acute effect Effects 0.000 description 2
- 230000006978 adaptation Effects 0.000 description 2
- 108010091628 alpha 1-Antichymotrypsin Proteins 0.000 description 2
- 150000001408 amides Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 208000005881 bovine spongiform encephalopathy Diseases 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000002490 cerebral effect Effects 0.000 description 2
- 210000001175 cerebrospinal fluid Anatomy 0.000 description 2
- 230000001684 chronic effect Effects 0.000 description 2
- 208000017580 chronic wasting disease Diseases 0.000 description 2
- IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000000295 emission spectrum Methods 0.000 description 2
- 238000001506 fluorescence spectroscopy Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229930004094 glycosylphosphatidylinositol Natural products 0.000 description 2
- 108010026364 glycyl-glycyl-leucine Proteins 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 238000010191 image analysis Methods 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 239000012678 infectious agent Substances 0.000 description 2
- 230000002458 infectious effect Effects 0.000 description 2
- 238000001990 intravenous administration Methods 0.000 description 2
- 206010023497 kuru Diseases 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 230000006984 memory degeneration Effects 0.000 description 2
- 208000023060 memory loss Diseases 0.000 description 2
- 210000002682 neurofibrillary tangle Anatomy 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- YBYRMVIVWMBXKQ-UHFFFAOYSA-N phenylmethanesulfonyl fluoride Chemical compound FS(=O)(=O)CC1=CC=CC=C1 YBYRMVIVWMBXKQ-UHFFFAOYSA-N 0.000 description 2
- 230000004481 post-translational protein modification Effects 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 108010015796 prolylisoleucine Proteins 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000012552 review Methods 0.000 description 2
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000002269 spontaneous effect Effects 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 230000014616 translation Effects 0.000 description 2
- 208000037956 transmissible mink encephalopathy Diseases 0.000 description 2
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 2
- 239000004474 valine Substances 0.000 description 2
- 125000002987 valine group Chemical group [H]N([H])C([H])(C(*)=O)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- RALAXQOLLAQGTI-IRGGMKSGSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-1-[(2s)-2-amino-4-methylpentanoyl]pyrrolidine-2-carbonyl]amino]-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]butanedioic acid Chemical compound CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC(O)=O)C(O)=O)CC1=CC=CC=C1 RALAXQOLLAQGTI-IRGGMKSGSA-N 0.000 description 1
- UHPQFNXOFFPHJW-UHFFFAOYSA-N (4-methylphenyl)-phenylmethanamine Chemical compound C1=CC(C)=CC=C1C(N)C1=CC=CC=C1 UHPQFNXOFFPHJW-UHFFFAOYSA-N 0.000 description 1
- BLXSFCHWMBESKV-UHFFFAOYSA-N 1-iodopentane Chemical compound CCCCCI BLXSFCHWMBESKV-UHFFFAOYSA-N 0.000 description 1
- ONEGZXHXCLCVRF-UHFFFAOYSA-N 2-[[2-[[1-(2-amino-3-methylbutanoyl)pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC(=O)C(C(C)C)NC(=O)C1CCCN1C(=O)C(N)C(C)C ONEGZXHXCLCVRF-UHFFFAOYSA-N 0.000 description 1
- CFBILACNYSPRPM-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;2-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]acetic acid Chemical compound OCC(N)(CO)CO.OCC(CO)(CO)NCC(O)=O CFBILACNYSPRPM-UHFFFAOYSA-N 0.000 description 1
- PDQGEKGUTOTUNV-TZSSRYMLSA-N 4'-deoxy-4'-iododoxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](I)[C@H](C)O1 PDQGEKGUTOTUNV-TZSSRYMLSA-N 0.000 description 1
- MQIGTEQXYCRLGK-BQBZGAKWSA-N Ala-Gly-Pro Chemical compound C[C@H](N)C(=O)NCC(=O)N1CCC[C@H]1C(O)=O MQIGTEQXYCRLGK-BQBZGAKWSA-N 0.000 description 1
- BFMIRJBURUXDRG-DLOVCJGASA-N Ala-Phe-Asp Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)C)CC1=CC=CC=C1 BFMIRJBURUXDRG-DLOVCJGASA-N 0.000 description 1
- JAQNUEWEJWBVAY-WBAXXEDZSA-N Ala-Phe-Phe Chemical compound C([C@H](NC(=O)[C@@H](N)C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 JAQNUEWEJWBVAY-WBAXXEDZSA-N 0.000 description 1
- MAZZQZWCCYJQGZ-GUBZILKMSA-N Ala-Pro-Arg Chemical compound [H]N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O MAZZQZWCCYJQGZ-GUBZILKMSA-N 0.000 description 1
- YHBDGLZYNIARKJ-GUBZILKMSA-N Ala-Pro-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)N YHBDGLZYNIARKJ-GUBZILKMSA-N 0.000 description 1
- 102000004400 Aminopeptidases Human genes 0.000 description 1
- 108090000915 Aminopeptidases Proteins 0.000 description 1
- 108010079054 Amyloid beta-Protein Precursor Proteins 0.000 description 1
- 102000014303 Amyloid beta-Protein Precursor Human genes 0.000 description 1
- 102000005666 Apolipoprotein A-I Human genes 0.000 description 1
- 108010059886 Apolipoprotein A-I Proteins 0.000 description 1
- 102000013918 Apolipoproteins E Human genes 0.000 description 1
- 108010025628 Apolipoproteins E Proteins 0.000 description 1
- TTXYKSADPSNOIF-IHRRRGAJSA-N Arg-Asp-Phe Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O TTXYKSADPSNOIF-IHRRRGAJSA-N 0.000 description 1
- FBLMOFHNVQBKRR-IHRRRGAJSA-N Arg-Asp-Tyr Chemical compound NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 FBLMOFHNVQBKRR-IHRRRGAJSA-N 0.000 description 1
- QLSRIZIDQXDQHK-RCWTZXSCSA-N Arg-Val-Thr Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)O)C(O)=O QLSRIZIDQXDQHK-RCWTZXSCSA-N 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- IOTKDTZEEBZNCM-UGYAYLCHSA-N Asn-Asn-Ile Chemical compound [H]N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O IOTKDTZEEBZNCM-UGYAYLCHSA-N 0.000 description 1
- WEDGJJRCJNHYSF-SRVKXCTJSA-N Asp-Cys-Phe Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)[C@H](CC(=O)O)N WEDGJJRCJNHYSF-SRVKXCTJSA-N 0.000 description 1
- JNNVNVRBYUJYGS-CIUDSAMLSA-N Asp-Leu-Ala Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(O)=O JNNVNVRBYUJYGS-CIUDSAMLSA-N 0.000 description 1
- AYFVRYXNDHBECD-YUMQZZPRSA-N Asp-Leu-Gly Chemical compound [H]N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O AYFVRYXNDHBECD-YUMQZZPRSA-N 0.000 description 1
- IVPNEDNYYYFAGI-GARJFASQSA-N Asp-Leu-Pro Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CC(=O)O)N IVPNEDNYYYFAGI-GARJFASQSA-N 0.000 description 1
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 1
- 238000011725 BALB/c mouse Methods 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 102100036597 Basement membrane-specific heparan sulfate proteoglycan core protein Human genes 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 125000001433 C-terminal amino-acid group Chemical group 0.000 description 1
- 108091016585 CD44 antigen Proteins 0.000 description 1
- 241000283707 Capra Species 0.000 description 1
- 241000700198 Cavia Species 0.000 description 1
- 102000029816 Collagenase Human genes 0.000 description 1
- 108060005980 Collagenase Proteins 0.000 description 1
- 108091035707 Consensus sequence Proteins 0.000 description 1
- 108010069514 Cyclic Peptides Proteins 0.000 description 1
- 102000001189 Cyclic Peptides Human genes 0.000 description 1
- CLDCTNHPILWQCW-CIUDSAMLSA-N Cys-Arg-Glu Chemical compound C(C[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC(=O)[C@H](CS)N)CN=C(N)N CLDCTNHPILWQCW-CIUDSAMLSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 102000007260 Deoxyribonuclease I Human genes 0.000 description 1
- 108010008532 Deoxyribonuclease I Proteins 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
- 206010016202 Familial Amyloidosis Diseases 0.000 description 1
- 206010016207 Familial Mediterranean fever Diseases 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 206010072075 Gerstmann-Straussler-Scheinker syndrome Diseases 0.000 description 1
- 206010018341 Gliosis Diseases 0.000 description 1
- QKWBEMCLYTYBNI-GVXVVHGQSA-N Gln-Lys-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CCC(N)=O QKWBEMCLYTYBNI-GVXVVHGQSA-N 0.000 description 1
- XQDGOJPVMSWZSO-SRVKXCTJSA-N Gln-Pro-Leu Chemical compound CC(C)C[C@@H](C(=O)O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCC(=O)N)N XQDGOJPVMSWZSO-SRVKXCTJSA-N 0.000 description 1
- NNQDRRUXFJYCCJ-NHCYSSNCSA-N Glu-Pro-Val Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(O)=O NNQDRRUXFJYCCJ-NHCYSSNCSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- PYTZFYUXZZHOAD-WHFBIAKZSA-N Gly-Ala-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)CN PYTZFYUXZZHOAD-WHFBIAKZSA-N 0.000 description 1
- PUUYVMYCMIWHFE-BQBZGAKWSA-N Gly-Ala-Arg Chemical compound NCC(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CCCN=C(N)N PUUYVMYCMIWHFE-BQBZGAKWSA-N 0.000 description 1
- SUDUYJOBLHQAMI-WHFBIAKZSA-N Gly-Asp-Cys Chemical compound NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CS)C(O)=O SUDUYJOBLHQAMI-WHFBIAKZSA-N 0.000 description 1
- LCNXZQROPKFGQK-WHFBIAKZSA-N Gly-Asp-Ser Chemical compound NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O LCNXZQROPKFGQK-WHFBIAKZSA-N 0.000 description 1
- PCPOYRCAHPJXII-UWVGGRQHSA-N Gly-Lys-Met Chemical compound [H]NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCSC)C(O)=O PCPOYRCAHPJXII-UWVGGRQHSA-N 0.000 description 1
- FEUPVVCGQLNXNP-IRXDYDNUSA-N Gly-Phe-Phe Chemical compound C([C@H](NC(=O)CN)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)C1=CC=CC=C1 FEUPVVCGQLNXNP-IRXDYDNUSA-N 0.000 description 1
- IRJWAYCXIYUHQE-WHFBIAKZSA-N Gly-Ser-Ala Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)CN IRJWAYCXIYUHQE-WHFBIAKZSA-N 0.000 description 1
- RIYIFUFFFBIOEU-KBPBESRZSA-N Gly-Tyr-Leu Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)CN)CC1=CC=C(O)C=C1 RIYIFUFFFBIOEU-KBPBESRZSA-N 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 229920002683 Glycosaminoglycan Polymers 0.000 description 1
- 102000008055 Heparan Sulfate Proteoglycans Human genes 0.000 description 1
- 108010022901 Heparin Lyase Proteins 0.000 description 1
- IDQNVIWPPWAFSY-AVGNSLFASA-N His-His-Gln Chemical compound [H]N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CCC(N)=O)C(O)=O IDQNVIWPPWAFSY-AVGNSLFASA-N 0.000 description 1
- OUUCIIJSBIBCHB-ZPFDUUQYSA-N Ile-Leu-Asp Chemical compound CC[C@H](C)[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O OUUCIIJSBIBCHB-ZPFDUUQYSA-N 0.000 description 1
- IVXJIMGDOYRLQU-XUXIUFHCSA-N Ile-Pro-Leu Chemical compound CC[C@H](C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O IVXJIMGDOYRLQU-XUXIUFHCSA-N 0.000 description 1
- RKQAYOWLSFLJEE-SVSWQMSJSA-N Ile-Thr-Cys Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CS)C(=O)O)N RKQAYOWLSFLJEE-SVSWQMSJSA-N 0.000 description 1
- 108060003951 Immunoglobulin Proteins 0.000 description 1
- 208000005531 Immunoglobulin Light-chain Amyloidosis Diseases 0.000 description 1
- 208000026350 Inborn Genetic disease Diseases 0.000 description 1
- 208000031430 Inherited human prion disease Diseases 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 1
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- 125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 description 1
- KGCLIYGPQXUNLO-IUCAKERBSA-N Leu-Gly-Glu Chemical compound CC(C)C[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCC(O)=O KGCLIYGPQXUNLO-IUCAKERBSA-N 0.000 description 1
- VWHGTYCRDRBSFI-ZETCQYMHSA-N Leu-Gly-Gly Chemical compound CC(C)C[C@H](N)C(=O)NCC(=O)NCC(O)=O VWHGTYCRDRBSFI-ZETCQYMHSA-N 0.000 description 1
- UCNNZELZXFXXJQ-BZSNNMDCSA-N Leu-Leu-Tyr Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 UCNNZELZXFXXJQ-BZSNNMDCSA-N 0.000 description 1
- MJWVXZABPOKJJF-ACRUOGEOSA-N Leu-Phe-Phe Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=CC=C1)C(O)=O MJWVXZABPOKJJF-ACRUOGEOSA-N 0.000 description 1
- UHNQRAFSEBGZFZ-YESZJQIVSA-N Leu-Phe-Pro Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N2CCC[C@@H]2C(=O)O)N UHNQRAFSEBGZFZ-YESZJQIVSA-N 0.000 description 1
- UCXQIIIFOOGYEM-ULQDDVLXSA-N Leu-Pro-Tyr Chemical compound CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 UCXQIIIFOOGYEM-ULQDDVLXSA-N 0.000 description 1
- XOEDPXDZJHBQIX-ULQDDVLXSA-N Leu-Val-Phe Chemical compound CC(C)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 XOEDPXDZJHBQIX-ULQDDVLXSA-N 0.000 description 1
- FDBTVENULFNTAL-XQQFMLRXSA-N Leu-Val-Pro Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)O)N FDBTVENULFNTAL-XQQFMLRXSA-N 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- YPLVCBKEPJPBDQ-MELADBBJSA-N Lys-Leu-Pro Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@H](CCCCN)N YPLVCBKEPJPBDQ-MELADBBJSA-N 0.000 description 1
- LJADEBULDNKJNK-IHRRRGAJSA-N Lys-Leu-Val Chemical compound CC(C)C[C@H](NC(=O)[C@@H](N)CCCCN)C(=O)N[C@@H](C(C)C)C(O)=O LJADEBULDNKJNK-IHRRRGAJSA-N 0.000 description 1
- YXPJCVNIDDKGOE-MELADBBJSA-N Lys-Lys-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)N)C(=O)O YXPJCVNIDDKGOE-MELADBBJSA-N 0.000 description 1
- YSPZCHGIWAQVKQ-AVGNSLFASA-N Lys-Pro-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCCN YSPZCHGIWAQVKQ-AVGNSLFASA-N 0.000 description 1
- CUHGAUZONORRIC-HJGDQZAQSA-N Lys-Thr-Asn Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)O)NC(=O)[C@H](CCCCN)N)O CUHGAUZONORRIC-HJGDQZAQSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 102000018697 Membrane Proteins Human genes 0.000 description 1
- 108010052285 Membrane Proteins Proteins 0.000 description 1
- HZVXPUHLTZRQEL-UWVGGRQHSA-N Met-Leu-Gly Chemical compound CSCC[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)NCC(O)=O HZVXPUHLTZRQEL-UWVGGRQHSA-N 0.000 description 1
- 241001529936 Murinae Species 0.000 description 1
- 241000699660 Mus musculus Species 0.000 description 1
- XZFYRXDAULDNFX-UHFFFAOYSA-N N-L-cysteinyl-L-phenylalanine Natural products SCC(N)C(=O)NC(C(O)=O)CC1=CC=CC=C1 XZFYRXDAULDNFX-UHFFFAOYSA-N 0.000 description 1
- KZNQNBZMBZJQJO-UHFFFAOYSA-N N-glycyl-L-proline Natural products NCC(=O)N1CCCC1C(O)=O KZNQNBZMBZJQJO-UHFFFAOYSA-N 0.000 description 1
- 206010029260 Neuroblastoma Diseases 0.000 description 1
- 208000008457 Neurologic Manifestations Diseases 0.000 description 1
- 108010043958 Peptoids Proteins 0.000 description 1
- HTTYNOXBBOWZTB-SRVKXCTJSA-N Phe-Asn-Asn Chemical compound C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC(=O)N)C(=O)O)N HTTYNOXBBOWZTB-SRVKXCTJSA-N 0.000 description 1
- DVOCGBNHAUHKHJ-DKIMLUQUSA-N Phe-Ile-Leu Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(O)=O DVOCGBNHAUHKHJ-DKIMLUQUSA-N 0.000 description 1
- ZLAKUZDMKVKFAI-JYJNAYRXSA-N Phe-Pro-Val Chemical compound [H]N[C@@H](CC1=CC=CC=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(O)=O ZLAKUZDMKVKFAI-JYJNAYRXSA-N 0.000 description 1
- JSGWNFKWZNPDAV-YDHLFZDLSA-N Phe-Val-Asp Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](N)CC1=CC=CC=C1 JSGWNFKWZNPDAV-YDHLFZDLSA-N 0.000 description 1
- 206010036105 Polyneuropathy Diseases 0.000 description 1
- 108010007288 PrPSc Proteins Proteins 0.000 description 1
- 206010036673 Primary amyloidosis Diseases 0.000 description 1
- APKRGYLBSCWJJP-FXQIFTODSA-N Pro-Ala-Asp Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](C)C(=O)N[C@@H](CC(O)=O)C(O)=O APKRGYLBSCWJJP-FXQIFTODSA-N 0.000 description 1
- XUSDDSLCRPUKLP-QXEWZRGKSA-N Pro-Asp-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H]1CCCN1 XUSDDSLCRPUKLP-QXEWZRGKSA-N 0.000 description 1
- LHALYDBUDCWMDY-CIUDSAMLSA-N Pro-Glu-Ala Chemical compound C[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H]1CCCN1)C(O)=O LHALYDBUDCWMDY-CIUDSAMLSA-N 0.000 description 1
- DXTOOBDIIAJZBJ-BQBZGAKWSA-N Pro-Gly-Ser Chemical compound [H]N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CO)C(O)=O DXTOOBDIIAJZBJ-BQBZGAKWSA-N 0.000 description 1
- AUQGUYPHJSMAKI-CYDGBPFRSA-N Pro-Ile-Val Chemical compound CC(C)[C@@H](C(O)=O)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@@H]1CCCN1 AUQGUYPHJSMAKI-CYDGBPFRSA-N 0.000 description 1
- CLJLVCYFABNTHP-DCAQKATOSA-N Pro-Leu-Asp Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(O)=O CLJLVCYFABNTHP-DCAQKATOSA-N 0.000 description 1
- DRKAXLDECUGLFE-ULQDDVLXSA-N Pro-Leu-Phe Chemical compound CC(C)C[C@H](NC(=O)[C@@H]1CCCN1)C(=O)N[C@@H](Cc1ccccc1)C(O)=O DRKAXLDECUGLFE-ULQDDVLXSA-N 0.000 description 1
- MCWHYUWXVNRXFV-RWMBFGLXSA-N Pro-Leu-Pro Chemical compound CC(C)C[C@@H](C(=O)N1CCC[C@@H]1C(=O)O)NC(=O)[C@@H]2CCCN2 MCWHYUWXVNRXFV-RWMBFGLXSA-N 0.000 description 1
- RMODQFBNDDENCP-IHRRRGAJSA-N Pro-Lys-Leu Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(O)=O RMODQFBNDDENCP-IHRRRGAJSA-N 0.000 description 1
- OOZJHTXCLJUODH-QXEWZRGKSA-N Pro-Val-Asp Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H]1CCCN1 OOZJHTXCLJUODH-QXEWZRGKSA-N 0.000 description 1
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 description 1
- 101000933967 Pseudomonas phage KPP25 Major capsid protein Proteins 0.000 description 1
- 102000007056 Recombinant Fusion Proteins Human genes 0.000 description 1
- 108010008281 Recombinant Fusion Proteins Proteins 0.000 description 1
- IYCBDVBJWDXQRR-FXQIFTODSA-N Ser-Ala-Met Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCSC)C(O)=O IYCBDVBJWDXQRR-FXQIFTODSA-N 0.000 description 1
- HQTKVSCNCDLXSX-BQBZGAKWSA-N Ser-Arg-Gly Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(O)=O HQTKVSCNCDLXSX-BQBZGAKWSA-N 0.000 description 1
- ZKBKUWQVDWWSRI-BZSNNMDCSA-N Ser-Phe-Tyr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O ZKBKUWQVDWWSRI-BZSNNMDCSA-N 0.000 description 1
- OLKICIBQRVSQMA-SRVKXCTJSA-N Ser-Ser-Tyr Chemical compound [H]N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O OLKICIBQRVSQMA-SRVKXCTJSA-N 0.000 description 1
- 108010045517 Serum Amyloid P-Component Proteins 0.000 description 1
- 101710190759 Serum amyloid A protein Proteins 0.000 description 1
- 108010032838 Sialoglycoproteins Proteins 0.000 description 1
- 102000007365 Sialoglycoproteins Human genes 0.000 description 1
- 108090000054 Syndecan-2 Proteins 0.000 description 1
- OGOYMQWIWHGTGH-KZVJFYERSA-N Thr-Val-Ala Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C)C(O)=O OGOYMQWIWHGTGH-KZVJFYERSA-N 0.000 description 1
- BPGDJSUFQKWUBK-KJEVXHAQSA-N Thr-Val-Tyr Chemical compound C[C@@H](O)[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 BPGDJSUFQKWUBK-KJEVXHAQSA-N 0.000 description 1
- 108700019146 Transgenes Proteins 0.000 description 1
- 239000007997 Tricine buffer Substances 0.000 description 1
- UNUZEBFXGWVAOP-DZKIICNBSA-N Tyr-Glu-Val Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(O)=O UNUZEBFXGWVAOP-DZKIICNBSA-N 0.000 description 1
- OFHKXNKJXURPSY-ULQDDVLXSA-N Tyr-Met-Leu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(C)C)C(O)=O OFHKXNKJXURPSY-ULQDDVLXSA-N 0.000 description 1
- BIWVVOHTKDLRMP-ULQDDVLXSA-N Tyr-Pro-Leu Chemical compound [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(O)=O BIWVVOHTKDLRMP-ULQDDVLXSA-N 0.000 description 1
- NYTKXWLZSNRILS-IFFSRLJSSA-N Val-Gln-Thr Chemical compound C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](C(C)C)N)O NYTKXWLZSNRILS-IFFSRLJSSA-N 0.000 description 1
- PIFJAFRUVWZRKR-QMMMGPOBSA-N Val-Gly-Gly Chemical compound CC(C)[C@H]([NH3+])C(=O)NCC(=O)NCC([O-])=O PIFJAFRUVWZRKR-QMMMGPOBSA-N 0.000 description 1
- YTUABZMPYKCWCQ-XQQFMLRXSA-N Val-His-Pro Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N2CCC[C@@H]2C(=O)O)N YTUABZMPYKCWCQ-XQQFMLRXSA-N 0.000 description 1
- VNGKMNPAENRGDC-JYJNAYRXSA-N Val-Phe-Arg Chemical compound NC(N)=NCCC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)C(C)C)CC1=CC=CC=C1 VNGKMNPAENRGDC-JYJNAYRXSA-N 0.000 description 1
- ZXYPHBKIZLAQTL-QXEWZRGKSA-N Val-Pro-Asp Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(=O)O)C(=O)O)N ZXYPHBKIZLAQTL-QXEWZRGKSA-N 0.000 description 1
- VSCIANXXVZOYOC-AVGNSLFASA-N Val-Pro-His Chemical compound CC(C)[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC2=CN=CN2)C(=O)O)N VSCIANXXVZOYOC-AVGNSLFASA-N 0.000 description 1
- USLVEJAHTBLSIL-CYDGBPFRSA-N Val-Pro-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)C(C)C USLVEJAHTBLSIL-CYDGBPFRSA-N 0.000 description 1
- 241000726445 Viroids Species 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 description 1
- 108010066829 alanyl-glutamyl-aspartylprolyine Proteins 0.000 description 1
- 108010005233 alanylglutamic acid Proteins 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 230000006933 amyloid-beta aggregation Effects 0.000 description 1
- 229940045799 anthracyclines and related substance Drugs 0.000 description 1
- 230000000389 anti-prion effect Effects 0.000 description 1
- 101150031224 app gene Proteins 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 235000009697 arginine Nutrition 0.000 description 1
- 108010052670 arginyl-glutamyl-glutamic acid Proteins 0.000 description 1
- 108010072041 arginyl-glycyl-aspartic acid Proteins 0.000 description 1
- 235000009582 asparagine Nutrition 0.000 description 1
- 229960001230 asparagine Drugs 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 108010047857 aspartylglycine Proteins 0.000 description 1
- 230000003140 astrocytic effect Effects 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- 102000015736 beta 2-Microglobulin Human genes 0.000 description 1
- 108010081355 beta 2-Microglobulin Proteins 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 238000002306 biochemical method Methods 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 210000005013 brain tissue Anatomy 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 201000004559 cerebral degeneration Diseases 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001149 cognitive effect Effects 0.000 description 1
- 231100000870 cognitive problem Toxicity 0.000 description 1
- 229960002424 collagenase Drugs 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 230000001086 cytosolic effect Effects 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 230000003412 degenerative effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
- 229940093471 ethyl oleate Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 210000001723 extracellular space Anatomy 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 201000006061 fatal familial insomnia Diseases 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 238000002795 fluorescence method Methods 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 238000012252 genetic analysis Methods 0.000 description 1
- 208000016361 genetic disease Diseases 0.000 description 1
- 230000007387 gliosis Effects 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 108010049041 glutamylalanine Proteins 0.000 description 1
- XBGGUPMXALFZOT-UHFFFAOYSA-N glycyl-L-tyrosine hemihydrate Natural products NCC(=O)NC(C(O)=O)CC1=CC=C(O)C=C1 XBGGUPMXALFZOT-UHFFFAOYSA-N 0.000 description 1
- 210000004884 grey matter Anatomy 0.000 description 1
- 238000001631 haemodialysis Methods 0.000 description 1
- 230000000322 hemodialysis Effects 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 108010038082 heparin proteoglycan Proteins 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 108010092114 histidylphenylalanine Proteins 0.000 description 1
- 208000010544 human prion disease Diseases 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000002163 immunogen Effects 0.000 description 1
- 230000005847 immunogenicity Effects 0.000 description 1
- 102000018358 immunoglobulin Human genes 0.000 description 1
- 238000003364 immunohistochemistry Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000011503 in vivo imaging Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 208000019143 inherited prion disease Diseases 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 1
- 108010078274 isoleucylvaline Proteins 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 238000004989 laser desorption mass spectroscopy Methods 0.000 description 1
- 108010044311 leucyl-glycyl-glycine Proteins 0.000 description 1
- 108010051673 leucyl-glycyl-phenylalanine Proteins 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000012417 linear regression Methods 0.000 description 1
- 235000018977 lysine Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 210000002418 meninge Anatomy 0.000 description 1
- 108020004999 messenger RNA Proteins 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 108091005601 modified peptides Proteins 0.000 description 1
- 108091005573 modified proteins Proteins 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 210000004898 n-terminal fragment Anatomy 0.000 description 1
- 230000009251 neurologic dysfunction Effects 0.000 description 1
- 230000007171 neuropathology Effects 0.000 description 1
- 231100000189 neurotoxic Toxicity 0.000 description 1
- 230000002887 neurotoxic effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 210000004940 nucleus Anatomy 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000007310 pathophysiology Effects 0.000 description 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
- 238000010647 peptide synthesis reaction Methods 0.000 description 1
- 230000010412 perfusion Effects 0.000 description 1
- 108010049224 perlecan Proteins 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- 108010024654 phenylalanyl-prolyl-alanine Proteins 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 230000007824 polyneuropathy Effects 0.000 description 1
- 238000011886 postmortem examination Methods 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 108010031719 prolyl-serine Proteins 0.000 description 1
- 108010070643 prolylglutamic acid Proteins 0.000 description 1
- 108010029020 prolylglycine Proteins 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011158 quantitative evaluation Methods 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000012723 sample buffer Substances 0.000 description 1
- 238000013391 scatchard analysis Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 230000009919 sequestration Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000003393 splenic effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 238000011830 transgenic mouse model Methods 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 108010003137 tyrosyltyrosine Proteins 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 210000004885 white matter Anatomy 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0821—Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
- C07K5/0823—Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp and Pro-amino acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/0004—Screening or testing of compounds for diagnosis of disorders, assessment of conditions, e.g. renal clearance, gastric emptying, testing for diabetes, allergy, rheuma, pancreas functions
- A61K49/0008—Screening agents using (non-human) animal models or transgenic animal models or chimeric hosts, e.g. Alzheimer disease animal model, transgenic model for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4711—Alzheimer's disease; Amyloid plaque core protein
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
- G01N33/6896—Neurological disorders, e.g. Alzheimer's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Definitions
- This invention relates to the field of therapeutic peptides for the prevention and treatment of disorders or diseases resulting from abnormal formation of amyloid or amyloid-like deposits, such as, but not limited to, prion-related encephalophathies, Alzheimer's dementia or disease (AD), and other amyloidosis disorders.
- This invention also relates to the use of the peptides in preventing the formation of or in promoting the redissolution of these insoluble amyloid or amyloid-like deposits.
- AD Alzheimer's disease
- amyloidogenesis insoluble fibrous masses
- amyloid ⁇ -peptide The main component of amyloid is a 4.1-4.3 kDa hydrophobic peptide, named amyloid ⁇ -peptide (A ⁇ ), that is codified in chromosome 21 as part of a much longer amyloid precursor protein APP (Muller-Hill and Beyreuther, Ann. Rev. Biochem. 38:287-307, 1989).
- the APP starts with a leader sequence (signal peptide), followed by a cysteine-rich region, an acidic-rich domain, a protease inhibitor motif, a putative N-glycosylated region, a transmembrane domain, and finally a small cytoplasmic region.
- the A ⁇ sequence begins close to the membrane on the extracellular side and ends within the membrane.
- AD familial form of AD
- Down's syndrome patients have three copies of APP gene and develop AD neuropathology at an early age (Wisniewski et al., Ann. Neurol. 17:278-282, 1985).
- Genetic analysis of families with hereditary AD revealed mutations in chromosome 21, near or within the A ⁇ sequence (Forsell et al., Neurosci. Lett. 184:90-93, 1995).
- BBB blood-brain barrier
- Peptides containing the sequence 1-40 or 1-42 of A ⁇ and shorter derivatives can form amyloid-like fibrils in the absence of other protein (Soto et al., J. Neurochem. 63:1191-1198, 1994), suggesting that the potential to form amyloid resides mainly in the structure of A ⁇ .
- the relation between the primary structure of A ⁇ and its ability to form amyloid-like fibrils was analyzed by altering the sequence of the peptide. Substitution of hydrophilic residues for hydrophobic ones in the internal A ⁇ hydrophobic regions (amino acids 17-21) impaired fibril formation (Hilbich et al., J. Mol. Biol. 228:460-473, 1992), suggesting that A ⁇ assembly is partially driven by hydrophobic interactions.
- a ⁇ peptides (A ⁇ 1-42/43) comprising two or three additional hydrophobic C-terminal residues are more amyloidogenic (Jarrett et al., Biochem 32:4693-4697, 1993).
- the conformation adopted by A ⁇ peptides is crucial in amyloid formation.
- a ⁇ incubated at different pH, concentrations and solvents has mainly an ⁇ -helical (random coil) or a ⁇ -sheet secondary structure (Barrow et al., J. Mol. Biol. 225:1075-1093, 1992: Burdick et al., J. Biol. Chem. 267:546-554, 1992; Zagorski et al., Biochem.
- the N-terminus may be a potential target site for inhibition of the initial random coil to ⁇ -sheet conformational change.
- a ⁇ amyloid formation is dependent on hydrophobic interactions of A ⁇ peptides adopting an antiparallel ⁇ -sheet conformation and that both the N- and C-terminal domains are important for amyloid formation.
- the basic unit of fibril formation appears to be the conformer adopting an antiparallel ⁇ -sheet composed of strands involving the regions 10-24 and 29-40/42 of the peptide (Soto et al., 1994, supra).
- Amyloid formation proceeds by intermolecular interactions between the ⁇ -strands of several monomers to form an oligomeric ⁇ -sheet structure precursor of the fibrillar 62 -cross conformation.
- inhibitory peptides of the present invention which inhibit the formation of amyloid deposits from native A ⁇ as opposed to solely preventing aggregation of a proline-modified modified peptide or protein, are not intended to include the peptides of Wood et al. having the amino acid sequences SEQ ID NOs: 50-65.
- AD Alzheimer's disease
- Heparin sulfate (glycosoaminoglycan) or the heparin sulfate proteoglycan, perlecan, has been identified as a component of all amyloids and has also been implicated in the earliest stages of inflammation-associated amyloid induction. Kisilevsky et al., Nature Medicine 1(2):143-148, (1995) describes the use of low molecular weight (135-1,000 Da) anionic sulfonate or sulfate compounds that interfere with the interaction of heparin sulfate with the inflammation-associated amyloid precursor and the ⁇ -peptide of AD.
- Heparin sulfate specifically influences the soluble amyloid precursor (SAA2) to adopt an increased ⁇ -sheet structure characteristic of the protein-folding pattern of amyloids.
- SAA2 soluble amyloid precursor
- These anionic sulfonate or sulfate compounds were shown to inhibit heparin-accelerated Alzheimer's A ⁇ fibril formation and were able to disassemble preformed fibrils in vitro as monitored by electron micrography.
- these compounds when administered orally at relatively high concentrations (20 or 50 mM), substantially arrested murine splenic inflammation-associated amyloid progression in vivo in acute and chronic models.
- the most potent compound, poly-(vinylsulfonate) was acutely toxic.
- IDOX Anthracycline 4′-iodo-4′-deoxy-doxorubicin
- AEF amyloid enhancing factor
- IDOX is also extremely toxic.
- This binding is distinct from heparin sulfate binding as removal of the glycosaminoglycans from extracted amyloid fibrils with heparinases did not modify IDOX binding.
- the common structural feature of all amyloids is a ⁇ -pleated sheet conformation.
- IDOX does not bind native amyloid precursor light chains which suggests that the ⁇ -pleated sheet backbone alone is not sufficient to form the optimal structure for IDOX binding, and that it is the fibril cross- ⁇ -sheet quaternary structure that is required for maximal IDOX binding. It has been found that the amount of IDOX extracted from spleens is correlated with amyloid load and not circulating serum precursor amyloid levels. IDOX, however, is also extremely toxic.
- APP amyloid precursor protein
- WO 9427603 Modulating proteolytic processing of APP to nucleating forms of AD has also been examined in AU 9338358 and EP569777.
- WO 95046477 discloses synthetic peptides of composition X-X-N-X (SEQ ID NO: 69) coupled to a carrier, where X is a cationic amino acid and N is a neutral amino acid, which inhibit A ⁇ binding to glycosoaminoglycan.
- Peptides containing Alzheimer's A ⁇ sequences that inhibit the coupling of ⁇ -1-antichymotrypsin and A ⁇ are disclosed in WO 9203474.
- Prions are the infectious particles responsible for a group of fatal neurodegenerative diseases known as spongiform encephalopathies (for reviews, see Prusiner & DeArmond, Annu. Rev. Neurosci. 17:311-339, 1994; Prusiner, Science 252:1515-1522, 1991).
- Creutzfeldt-Jakob disease (CJD) kuru
- CJD Creutzfeldt-Jakob disease
- GSS Gerstmann-Straussler syndrome
- Familial CJD and GSS are also genetic disorders. In addition to the prion diseases in humans, four disorders of animals are included in this type of disease.
- Bovine spongiform encephalopathy also known as the “mad cow disease”, transmissible mink encephalopathy, and chronic wasting disease of captive mule deer and elk are all thought to result from the ingestion of scrapie-infected animal products.
- PrP sc glycoprotein
- Prion replication is hypothesized to occur when PrP sc in the infecting inoculum interacts specifically with host PrP c (normal cellular PrP isoform), catalyzing its conversion to the pathogenic form of the protein (Cohen, F. E. et al., Science 264:530-531, 1994). It is postulated that this conversion takes place spontaneously in PrP molecules carrying mutations that have been linked to familial forms of prion disease.
- the cellular prion protein is a sialoglycoprotein encoded by a gene that in humans is located on chromosome 20 (Oesch, B. et al., Cell 40:735-746, (1985); Basler, K. et al., 46:417-428 (1986); Liao, Y. J. et al., Science 233:364-367 (1986); Meyer, R. K. et al., Proc. Natl. Acad. Sci. USA 83:2310-2314 (1986); Sparkes, R. S. et al., Proc. Natl. Acad. Sci.
- PrP gene is expressed in neural and non-neural tissues, the highest concentration of mRNA being in neurons (Chesebro, B. et al., Nature 315:331-333 (1985); Kretzschmar, H. A. et al., Am. J. Pathol. 122:1-5 (1986); Brown, H. R. et al., Acta Neuropathol. 80:1-6 (1990); Cashman, N. R. et al., Cell 61:185-192 (1990); Bendheim, P. E., Neurology 42:149-156 (1992)).
- the translation product of the PrP gene consists of 253 amino acids in humans (Kretzschmar, H. A. et al., DNA 5:315-324 (1986); Pucket, C. et al., Am. J. Hum. 49:320-329 (1991)), 254 in hamster and mice or 256 amino acids in sheep and undergoes several post-translational modifications.
- a signal peptide of 22 amino acids is cleaved at the N-terminus, 23 amino acids are removed from the C-terminus on addition of a glycosyl phosphatidylinositol (GPI) anchor, and asparagine-linked oligosaccharides are attached to residues 181 and 197 in a loop formed by a disulfide bond (Turk, E. et al., Eur. J. Biochem. 176:21-30 (1988); Hope, J. et al., EMBO J. 5:2591-2597 (1986); Stahl, N. et al., Cell 51:229-240 (1987); Stahl, N. et al., Biochemistry 29:5405-5412 (1990); Safar, J. et al., Proc. Natl. Acad. Sci. USA 87:6377 (1990)).
- GPI glycosyl phosphatidylinositol
- PrP c normal cellular isoform
- PrP Sc normal cellular isoform
- PrP sc is insoluble in physiological solvents and forms aggregates; (2) PrP sc is partially resistant to proteolytic degradation by proteinase K in that only the N-terminal 67 amino acids are removed by proteinase K digestion under conditions in which prP c is completely degraded, and which results in a N-terminally truncated form known as PrP27-30; and (3) PrP sc has an alteration in protein conformation from ⁇ -helical for PrP c to an altered form which is rich in ⁇ -sheet secondary structure.
- PrP sc is a major and necessary component of the infectious prion (reviewed in Prusiner, S. B. Science 252:1515-1522, 1991) and are as follows: (a) copurification of PrP27-30 and scrapie infectivity were determined by biochemical methods where the concentration of PrP27-30 is proportional to prion titer; (b) kinetics of proteolytic digestion of PrP27-30 and infectivity are similar; (c) copurification of PrP sc and infectivity were observed using immunoaffinity; (d) infectivity was neutralized by anti-PrP antibodies; (e) detection of PrP sc were only detected in clones of cultured cells producing infectivity; (f) most, if not all, of the familial cases of PrP-related disorders are linked to mutations in the PrP gene; (g) mice expressing PrP genes with point mutations linked to GSS spontaneously develop neurologic dysfunction, spongiform brain degeneration and
- PrP sc the protease-resistant core of PrP sc is the major structural protein of amyloid fibrils that accumulate intracerebrally in some of these conditions (Brendheim, P. E. et al., Nature 310:418-421 (1984); DeArmond, S. J. et al., Cell 41:221-235 (1985); Kitamoto, T. et al., Ann. Neurol. 20:204-208 (1986); Robert, G. W. et al., N. Engl. Med. 315:1231-1233 (1986); Ghetti, B. et al., Neurology 39:1453-1461 (1989); Tagliavini, F. et al., EMBO J. 10:513-519 (1991); Kitamoto, T. et al., Neurology 41:306-310 (1991)).
- both diseases are similar, including memory loss, behavioral abnormalities, cognitive problems and dementia;
- both disorders are characterized clinically by age-related sporadic and familial forms of the disease;
- an abnormal form of a neuronal membrane protein (Amyloid- ⁇ precursor protein and PrP) appears to play a key role in the pathogenesis of both diseases;
- both A ⁇ and PrP are amyloidogenic and neurotoxic;
- an important part of the cases affected by familial prion disease typically develop neuritic plaques similar to the AD plaques, but containing PrP (instead of A ⁇ ) amyloid cores;
- a hallmark event in both diseases is the conformational transition from an ⁇ -helical-random coil structure to a ⁇ -sheet conformation in either PrP or A ⁇ .
- the present invention relates to novel inhibitory peptides capable of interacting or binding to a hydrophobic ⁇ -sheet forming cluster on a protein or peptide which forms amyloid or amyloid-like deposits so as to inhibit or structurally block the abnormal folding of the protein or peptide into a pathological ⁇ -sheet structure to form an amyloid or amyloid-like deposit, or a precursor thereof, such as is observed in Alzheimer's disease, amyloidosis disorders, prion-related encephalophathies, etc.
- the peptide includes a hydrophobic portion having one or more ⁇ -sheet blocking amino acid residues, and may also include charged amino acids at one or both ends of the peptide.
- inhibitory peptides have a low probability of adopting a ⁇ -sheet conformation and are capable of associating with said hydrophobic ⁇ -sheet forming cluster on the protein or peptide to structurally block and inhibit the abnormal folding thereof into amyloid or amyloid-like deposits, or pathological ⁇ -sheet precursors of amyloid or amyloid-like deposits.
- the present invention also relates to a method of preventing or treating a disorder or disease associated with the formation of amyloid or amyloid-like deposits involving the abnormal folding of a protein or peptide having a hydrophobic ⁇ -sheet forming cluster into a ⁇ -sheet structure, by administering an effective amount of such an inhibitory peptide to a subject in need thereof to prevent or reverse the abnormal folding of the protein or peptide into amyloid or amyloid-like deposits or pathological ⁇ -sheet precursors thereof.
- the present invention further relates to pharmaceutical compositions for the prevention or therapeutic treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits and pathological ⁇ -sheet-rich precursors thereof, using such inhibitory peptides.
- the present invention also relates to a method for detecting disorders or diseases associated with amyloid or amyloid-like fibril deposits and pathological ⁇ -sheet-rich precursors thereof.
- FIGS. 1 A-B provide a consensus sequence for amyloidogenesis in terms of hydrophobicity and secondary structure properties.
- FIG. 1A is the primary structure of the amyloidogenic sequence of peptides involved in the formation of several amyloid deposits.
- amyloid ⁇ -peptide found in Alzheimer's disease, its Dutch variant and Downs Syndrome
- amyloid A found in secondary amyloidosis and familial Mediterranean fever
- gelsolin amyloid SEQ ID NO: 3 related to familial amyloidosis of Finnish type
- amyloid L found in immunoglobulin-related primary amyloidosis
- ⁇ 2-microglobulin amyloid SEQ ID NO: 5 found in patients with chronic hemodialysis-related amyloidosis
- apolipoprotein A1 amyloid SEQ ID NO: 6 related to familial amyloidotic polyneuropathy.
- FIG. 1B provides the ⁇ -sheet prediction for the 15 amino acid fragments containing the sequences shown in FIG. 1A.
- the solid bar represents regions with a high probability of adopting a ⁇ -sheet structure.
- FIGS. 2 A-B provide the amino acid sequence for several anti-amyloid peptides.
- FIG. 2A shows the amino acid sequences four anti-amyloid peptides labeled as anti-amyloid 1 (SEQ ID NO: 7), anti-amyloid 2 (SEQ ID NO: 8), anti-amyloid 3 (SEQ ID NO: 9) and anti-amyloid 4 (SEQ ID NO: 10). Hydro-phobic amino acids are highlighted in bold.
- FIG. 2B shows the circular dichroism spectrum of the anti-amyloid peptide 1 (SEQ ID NO: 7) recorded as described in Example 1.
- FIG. 3 is a schematic representation of the ⁇ -cross conformation for amyloid fibrils showing the crucial importance of the interactions by hydrogen bonding between the monomeric ⁇ -strand to form the intermolecular ⁇ -cross structure.
- FIGS. 4 A-B show the effect of anti-amyloid peptide 2 having the sequence of SEQ ID NO: 8 on the amyloid formation by A ⁇ in vitro. Amyloid formation was quantitated by the fluorometric assay described in Example 1.
- FIG. 4A shows the dose-dependent inhibition of amyloidogenesis, using anti-amyloid peptide 2 (shown as filled squares) and a 12 amino acid-non related peptide as a control (shown as unfilled square). The incubation time was 24 hours at room temperature and the A ⁇ concentration was 1 mg/ml in 0.1 M Tris, pH 7.4.
- FIG. 4B shows the effect of anti-amyloid peptide 2 (SEQ ID NO: 8) on the amyloid formation after various incubation times.
- FIGS. 5 A-C show electron micrographs of negative-stained preparations of A ⁇ (FIG. 5A), A ⁇ incubated with anti-amyloid peptide 1 (SEQ ID NO: 7: FIG. 5B) and anti-amyloid peptide 1 alone (FIG. 5C). Aliquots of A ⁇ were incubated at 1 mg/ml with or without the anti-amyloid peptide 1 in a molar ratio 1:50 (A ⁇ :anti-amyloid) for 6 days at room temperature.
- FIGS. 6 A-B show the effects of anti-amyloid peptide 1 on the redissolution of preformed fibrils.
- Amyloid fibrils were formed by incubating A ⁇ (1 mg/ml) for 3 days at room temperature. Anti-amyloid peptide 1 was then added in a molar ratio 1:50 (A ⁇ :anti-amyloid peptide 1). The incubation was continued for 15 minutes, 6 hours or 24 hours and the amyloid formation was quantitated by the fluorometric assay (FIG. 6A). Fluorescence values represent the amount of amyloid formed.
- FIG. 6B provides electron micrographs of the nonincubated (left side picture) and incubated fibrils for 24 hours with anti-amyloid peptide 1 (right side picture). Magnification is 50,000 ⁇ .
- FIGS. 7 A-C show the physio-chemical characterization of the amphoterin (HMG-1) derived amyloid fragment, ATN p .
- FIG. 7A provides the amino acid sequence of the fragment ATN p (SEQ ID NO: 11). Hydrophobic amino acid residues are highlighted in bold.
- FIG. 7B shows the Chou-Fasman prediction for ⁇ -sheet structure of ATN p . The sequence with the highest ⁇ -sheet structure probability is indicated with a bar.
- FIG. 7C is an electron micrograph of negative-stained preparations of ATN p with formed amyloid-like fibrils.
- FIG. 8 is a bar graph showing the effect of anti-amyloid peptide 1 on the amyloid formation by A ⁇ and of peptides derived from the amyloidogenic sequence of gelsolin amyloid and amyloid A.
- Either A ⁇ or the fifteen amino acid peptides containing the amyloidogenic sequence of gelsolin amyloid (SEQ ID NO: 12) and amyloid A (SEQ ID NO: 13) were incubated in a concentration of 1 mg/ml for 24 hours without and with anti-amyloid peptide 1 in a molar ratio of 1:5 or 1:20.
- FIG. 9 shows the structural characteristics of anti-amyloid peptide 2(iA ⁇ ).
- the amino acid sequence and ⁇ -sheet probability for iA ⁇ (SEQ ID NO: 8) and for the region of A ⁇ (SEQ ID NO: 14) used as a template for iA ⁇ is shown underneath the ⁇ -sheet probability profile where the solid bar represents the region of A ⁇ having a high probability of ⁇ -sheet structure.
- FIG. 10 shows the circular dichroism spectra of iA ⁇ at different peptide concentration.
- FIG. 11 shows the A ⁇ -iA ⁇ interaction as quantitated by the quenching of the intrinsic fluorescence of A ⁇ (tyrosine 10) induced by the binding of iA ⁇ .
- the inset shows the fluorescence spectra of A ⁇ incubated alone or in the presence of 4 ⁇ M iA ⁇ .
- FIG. 12 shows the dose-dependent inhibition of A ⁇ 1-40 and A ⁇ 1-42 fibrillogenesis by iA ⁇ .
- Amyloid formation was quantitated by the fluorometric assay, as described in Example 1.
- the A ⁇ concentration was 1 mg/ml in 0.1M Tris, pH 7.6 and an incubation time of 24 h.
- FIG. 13 shows the effect of iA ⁇ on amyloid formation by A ⁇ 1-40, after different incubation periods.
- the molar ratio A ⁇ :iA ⁇ (or control) was 1:20; A ⁇ concentration 1 mg/ml.
- Amyloid formation was quantitated as in FIG. 12.
- iA ⁇ or the control peptide alone did not give fluorescence values above the background level.
- FIGS. 14A and 14B shows the dissolution of preformed A ⁇ fibrils by iA ⁇ in vitro.
- Amyloid fibrils were first preformed by incubating A ⁇ 1-40 or A ⁇ 1-42 at a concentration of 1 mg/ml for 6 days at room temperature. Fluorometric quantitation of amyloid as described in Example 1.
- FIG. 14A shows the effect of different molar ratios of iA ⁇ or control peptide on fibril disassembly after 24 h of incubation.
- FIG. 14B fibril dissolution induced by a 40-fold molar excess of iA ⁇ or control peptide after different incubation periods at room temperature.
- FIG. 15 a shows the electron microscopy analysis of the effect of iA ⁇ on fibril formation and dissolution.
- Aliquots of A ⁇ 1-40 (2 mg/ml) were incubated at 37° C. with or without iA ⁇ or control peptide at a molar ratio 1:40 (A ⁇ :iA ⁇ ), centrifuged and the pellet loaded on electron microscopy grids, stained and visualized as described in the Materials and Methods.
- FIG. 15 a shows A ⁇ incubated for 6 days;
- FIG. 15 b shows A ⁇ incubated with iA ⁇ for 6 days;
- FIG. 15 c shows A ⁇ incubated alone for 5 days and then for 1 day with iA ⁇ ;
- FIG. 15 d shows iA ⁇ incubated for 6 days at the same concentration as in FIGS. 15 b and c ;
- FIG. 15 e shows A ⁇ incubated with the control peptide for 6 days; and
- FIG. 15 f shows control peptide incubated alone for 6 days at the same concentration used in FIG. 15 e.
- FIG. 16 shows the inhibition of amyloid formation after long period of incubation (days) in the presence of low concentrations of iA ⁇ .
- 30 ⁇ g of A ⁇ 1-42 was incubated in 30 ⁇ l of 0.1M tris, pH 7.4 with a molar ratio 1:5 (A ⁇ :iA ⁇ ) of the inhibitor for different times at room temperature.
- Amyloid was quantitated by the thioflavine T fluorometric assay and expressed as a percentage of the amount of amyloid incubated for the same time in the absence of the inhibitor.
- FIG. 17 shows the inhibition of A ⁇ fibrillogenesis by iA ⁇ containing all D-amino acids.
- FIG. 18 shows the effect of iA ⁇ on the promotion of A ⁇ fibrillogenesis induced by apolipoprotein E.
- 30 ⁇ g of A ⁇ 1-40 were incubated with or without 2.4 ⁇ g of human plasma apolipoprotein E (apoE).
- Samples of A ⁇ alone or A ⁇ /apoE were incubated also with 1:10 (A ⁇ :iA ⁇ ) of the inhibitor. All the incubations were performed for 24 h at room temperature.
- Amyloid formation was evaluated by the thioflavine T fluorometric assay. The average of two different experiments is shown.
- FIG. 19 shows Alzheimer's amyloid plaque dissolution by iA ⁇ .
- FIG. 20 shows the effect of iA ⁇ on the A ⁇ -induced cell toxicity.
- FIG. 21 shows the change in the conformation of the PrP 109-141 fragment as evaluated by circular dichroism at time points of 0, 1, 3, 5, 7 and 10 days.
- FIG. 22 shows samples of the PrP 109-141 fragment in a random coil or ⁇ -sheet conformation being treated with proteinase K and electrophoresed on SDS polyacrylamide gel. Arrows on the left indicate the position of molecular weight standards.
- FIGS. 23A and 23B show the effect of the presence (FIG. 23B) or absence (FIG. 23A) of peptide iPrP-12aa on PrP109-141 fibrillogenesis as evaluated by electron microscopy.
- FIG. 24 shows the dose-dependent inhibition of PrP106-126 peptide fibrillogenesis by iPrP-12aa.
- the control peptide is CP1 (SEQ ID NO: 49).
- FIG. 25 shows the influence of iPrP-12aa on proteinase K degradation of PrP109-141 as determined by SDS-PAGE.
- Aliquots of PrP109-141 were converted from random coil to ⁇ -sheet by incubation for 7 days under the conditions described in Example 2 for the circular dichroism study in the absence (lane 3) or in the presence of 10-fold molar excess of an unrelated control peptide (CP1) (lane 4) or iPrP-12aa (lane 5). The sample was then lyophilized and resuspended in PBS.
- CP1 unrelated control peptide
- iPrP-12aa lane 5
- Novel peptides specifically designed to interfere with the ⁇ -sheet conformation of precursor proteins or peptides involved in the formation of amyloid or amyloid-like deposits have been developed.
- the present invention is directed to these novel peptides, pharmaceutical compositions containing one or a mixture of such peptides of the invention, and methods for preventing, treating, or detecting disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits or precursors thereof having a pathological ⁇ -sheet structure.
- the hydrophobic ⁇ -sheet forming cluster is believed to determine the binding of protein or peptide monomers resulting in aggregation, whereas the ⁇ -sheet potential of the longer sequence, of which the hydrophobic ⁇ -sheet forming cluster is a part, is believed to control the ordering of the aggregates into a ⁇ -cross conformation ( ⁇ -cross quaternary fibril structure) typical of amyloid fibril structure (FIG. 3).
- ⁇ -cross quaternary fibril structure typical of amyloid fibril structure
- Even a non-amyloid related peptide, which contains a potential amyloidogenic sequence motif (FIGS. 7A and 7B) such as obtained by proteolysis of amphoterin, forms typical amyloid-like fibrils in vitro (FIG. 7C).
- novel peptides of the present invention contain a hydrophobic portion or segment of at least three amino acid residues, where this portion is interrupted by one or more ⁇ -sheet blocking amino acid residues without substantially changing the hydrophobicity of the portion.
- these novel peptides can contain more than three hydrophobic amino acid residues within this portion, and/or contain other amino acid residues within this cluster or outside of it that also act to lower the propensity of the peptides of the present invention to adopt a ⁇ -sheet conformation.
- the peptides capable of interacting or binding with a structural determinant having a hydrophobic ⁇ -sheet forming cluster of amino acid residues on a protein or peptide involved in amyloid or amyloid-like deposit formation, which inhibits the abnormal folding of such a protein or peptide are designed with a knowledge of the structural determinants for amyloid, amyloid-like deposits, or pathological ⁇ -sheet precursor formation by prediction of a hydrophobic ⁇ -sheet forming cluster and/or by experimental confirmation of ⁇ -sheet conformation.
- prior identification of the structural determinant is not always necessary.
- Peptides having a hydrophobic ⁇ -sheet blocking portion which interacts with a hydrophobic ⁇ -sheet forming determinant of the protein or peptide, but with a very low probability of adopting a ⁇ -sheet conformation themselves, are designed to bind to the structural determinant and to function as an inhibitor of the conformational change resulting in the pathological ⁇ -sheet rich precursors of amyloid fibril formation and/or as an agent that dissolves preformed amyloid fibrils.
- one or more charged amino acid residue such as aspartic acid, glutamic acid, arginine, or lysine, can be placed at one or both ends of the peptide to increase the solubility of the inhibitory peptide.
- the inhibitory peptides of the invention contain one or more ⁇ -sheet blocking amino acids, such as Pro, Gly, Asn, or His, either within the hydrophobic portion containing at least three amino acid residues or immediately adjacent to this portion so as to prevent the binding of protein or peptide monomers into aggregates and the ordering of such aggregates into an altered conformation such as the ⁇ -cross conformation typical of amyloid fibril structure.
- ⁇ -sheet blocking amino acids such as Pro, Gly, Asn, or His
- peptides can be designed to be preferably homologous or partially homologous to the hydrophobic ⁇ -sheet forming cluster as the structural determinant they are to interact with, amino acid homology is not absolutely required as long as the peptide has a portion of sufficient hydrophobicity so that it will interact strongly with the hydrophobic ⁇ -sheet forming cluster to structurally block abnormal protein or peptide folding into fibril deposits or pathological ⁇ -sheet-rich precursors thereof.
- inhibitory peptides of the present invention it is important not only to have a hydrophobic portion or cluster that can interact and bind to the hydrophobic ⁇ -sheet forming cluster of the amyloidogenic protein or peptide, but also to introduce one or more ⁇ -sheet blocking amino acid residues.
- the hydrophobicity of the inhibitory peptide facilitates the binding interaction with the amyloidogenic protein or peptide
- a peptide is designed so that a hydrophobic portion of at least three amino acids is homologous to the hydrophobic ⁇ -sheet forming cluster predicted or identified experimentally to be involved in abnormal protein folding into a ⁇ -sheet structure.
- Highly hydrophobic amino acid residues of the hydrophobic ⁇ -sheet forming cluster are generally incorporated into the sequence of the homologous hydrophobic portion of the inhibitory peptide.
- any non-hydrophobic or poorly hydrophobic amino acid residues in the hydrophobic ⁇ -sheet forming cluster can be incorporated into the homologous hydrophobic portion, or deleted, or replaced with another amino acid such as a ⁇ -sheet blocking residue, preferably proline.
- the homologous hydrophobic portion of the inhibitory peptide has one or more ⁇ -sheet blocking residues that interrupt the homology to the hydrophobic ⁇ -sheet forming cluster by avoiding the presence of more than three contiguous amino acids within the homologous hydrophobic portion which are 100% homologous to the corresponding contiguous amino acids in the hydrophobic ⁇ -sheet forming cluster.
- the propensity or potential for forming a ⁇ -sheet conformation is dramatically reduced for the hydrophobic portion and for the inhibitory peptide as a whole, while the degree of hydrophobicity of the hydrophobic portion is kept substantially unchanged from that of the hydrophobic ⁇ -sheet forming cluster.
- This provides for the capability of the inhibitory peptide to hydrophobically interact/bind with the amyloidogenic protein or peptide where the ⁇ -sheet blocking capability of the designed inhibitory peptide is allowed to manifest itself by inhibiting the formation of ⁇ -sheet structures characteristic of amyloid or amyloid-like deposits and precursors thereof.
- An additional design parameter that is to be considered is the addition of charged amino acid residues at one or both ends of the inhibitory peptide which act mainly to increase the solubility of the peptide in an aqueous medium. This feature is more important with longer peptides and while preferred, is not absolutely necessary in short peptides.
- Prion protein PrP normally assumes an a-helical conformation, but abnormal protein folding alters the normal PrP conformation to an abnormal ⁇ -sheet conformation.
- inhibitor peptides are designed to bind to PrP to prevent abnormal protein folding into an altered conformation that would result in amyloid or amyloid-like deposits or pathological ⁇ -sheet precursors thereof, and thus can be used in the treatment of PrP diseases.
- Non-limiting examples of peptides designed to inhibit abnormal folding in the formation of amyloid and amyloid-like deposits, or pathological ⁇ -sheet precursors thereof are presented in Table 1.
- the anti-PrP peptides are designed to bind to the hydrophobic ⁇ -sheet forming structural determinant of PrP corresponding to amino acid residues 114 to 125 of prion (presented as SEQ ID NO: 23).
- Pro is used as the preferred ⁇ -sheet blocking amino acid in virtually all the peptides presented in Table 1, other ⁇ -sheet blockers, such as Gly (exemplified in the peptide of SEQ ID NO: 48), Asn and His, are suitable.
- Anti-amyloid peptides SEQ ID NO: 7 SEQ ID NO: 8 (iA ⁇ ) SEQ ID NO: 9 SEQ ID NO: 10 a) shorter derivatives of iA ⁇ (SEQ ID NO: 8) SEQ ID NO: 15 SEQ ID NO: 16 SEQ ID NO: 17 SEQ ID NO: 18 SEQ ID NO: 19 Pro-Phe-Phe SEQ ID NO: 27 SEQ ID NO: 28 SEQ ID NO: 29 SEQ ID NO: 30 SEQ ID NO: 31 SEQ ID NO: 32 SEQ ID NO: 33 SEQ ID NO: 49 b) derivatives of iA ⁇ with higher hydrophobicity SEQ ID NO: 20 SEQ ID NO: 21 SEQ ID NO: 22 2.
- Anti-prion (PrP) peptides SEQ ID NO: 24 SEQ ID NO: 25 SEQ ID NO: 38 SEQ ID NO: 39 SEQ ID NO: 40 SEQ ID NO: 41 SEQ ID NO: 42 SEQ ID NO: 43 SEQ ID NO: 44 SEQ ID NO: 45 SEQ ID NO: 46 SEQ ID NO: 47
- a specific non-limiting example of the general preferred design approach described above for designing A ⁇ inhibitory peptides according to the present invention first identifies the hydrophobic ⁇ -sheet forming cluster of A ⁇ , Leu Val Phe Phe Ala (corresponding to residues 2-6 of SEQ ID NO: 1).
- the alanine residue which is poorly hydrophobic can be replaced with the preferred ⁇ -sheet blocker, proline, or can be deleted altogether.
- the A ⁇ inhibitory peptide in Table 1 having the sequence of SEQ ID NO: 18 is designed to be homologous to amino acid residues 2-6 of SEQ ID NO: 1 where a proline ⁇ -sheet blocking residue is substituted for the valine residue, and a charged aspartic acid residue is placed at the end of the peptide.
- This peptide has a ⁇ -sheet blocker interrupting the hydrophobic ⁇ -sheet forming cluster of A ⁇ such that there are no more than three contiguous amino acids corresponding to the hydrophobic ⁇ -sheet forming cluster in the hydrophobic portion of the A ⁇ inhibitory peptide.
- a ⁇ inhibitory peptide of SEQ ID NO: 18 have a low ⁇ -sheet forming potential, but it also substantially retains the hydrophobicity of the hydrophobic ⁇ -sheet forming cluster corresponding to residues 2-6 of SEQ ID NO: 1.
- the charged aspartic acid residue at the end improves the solubility of the peptide.
- proline can be designed to replace one of the phenylalanine residues to yield A ⁇ inhibitory peptides having the sequences of SEQ ID NOs: 27 and 28.
- Another possibile design to insert a valine into the sequence of SEQ ID NO: 18 to arrive at an inhibitory peptide having the sequence of SEQ ID NO: 17.
- Modifications to amino acids in the peptides of the invention include, but are not limited to, an amide moiety or a pyroglutamyl residue. These modifications may contribute to decreasing the propensity to form ⁇ -sheet conformation or may contribute to peptide stability, solubility, or even immunogenicity. A more stable, soluble and less immunogenic peptide is desirable. Many neuropeptides modified at the C-terminus with a CONH 2 (amide) group appear to be resistant to attack by carboxypeptidases and many neuropeptides having a pyroglutamyl residue at the N-terminus are more resistant to attack by broad specificity amino peptides. Also included as peptides of the present invention are cyclic peptides that are resistant to attack by both carboxypeptidases and aminopeptidases.
- the inhibitory peptide of the present invention is administered in an effective amount to a subject in need thereof, where the subject can be human or animal.
- a method of detecting such disorders or diseases also includes administering a sufficient amount of the designed peptide to visualize its binding to fibril deposits or precursors thereof by well-known imaging techniques.
- peptides inhibitory to the formation of amyloid deposits in Alzheimer's disease can be preferably complexed with apolipoprotein J, as described in Zlokovic et al., Biochem. Biophys. Res. Commun. 205:1431-1437, (1994) and Proc. Natl. Acad. Sci. USA 93:4229-4234 (1996).
- Apolipoprotein J is believed to be a normal carrier for transport of A ⁇ into the brain parenchyma.
- the region responsible for interacting with apolipoprotein J in A ⁇ is the sequence corresponding to residues 17-25 of A ⁇ (SEQ ID NO: 1). Since this sequence is used as a template for the design of A ⁇ inhibitor peptides, these inhibitor peptides are expected to also be capable of interacting with apolipoprotein J and be transported across the blood-brain barrier using the receptor for apoJ.
- prevention of a condition such as Alzheimer's disease or other amyloidosis disorders
- a subject involves administering a peptide according to the present invention prior to the clinical onset of the disease.
- Treatment involves administration of the protective peptide after the clinical onset of the disease.
- successful administration of the peptide of the present invention, after development of a disorder or disease comprises “treatment” of the disease.
- the invention is useful in the treatment of humans as well as for veterinary uses in animals.
- the peptides of the present invention may be administered by any means that achieves its intended purpose.
- administration may be by a number of different parenteral routes including, but not limited to, subcutaneous, intravenous, intradermal, intramuscular, intraperitoneal, intracerebral, intranasal, oral, transdermal, or buccal routes.
- Parenteral administration can be bolus injection or by gradual perfusion over time.
- a typical regimen for preventing, suppressing, or treating a condition associated with amyloid or amyloid-like deposits comprises either (1) administration of an effective amount in one or two doses of a high concentration of inhibitory peptides in the range of 0.5 to 10 mg of peptide, more preferably 0.5 to 5 mg of peptide, or (2) administration of an effective amount of the peptide administered in multiple doses of lower concentrations of inhibitor peptides in the range of 10-1000 ⁇ g, more preferably 50-500 ⁇ g over a period of time up to and including several months to several years.
- the dosage administered will be dependent upon the age, sex, health, and weight of the recipient, kind of concurrent treatment, if any, frequency of treatment, and the nature of the effect desired.
- the total dose required for each treatment may be administered by multiple doses or in a single dose.
- effective amount it is meant a concentration of inhibitor peptide(s) which is capable of slowing down or inhibiting the formation of amyloid or amyloid-like deposits, or pathological ⁇ -sheet precursors thereof, or of dissolving preformed fibril deposits. Such concentrations can be routinely determined by those of skill in the art. It will also be appreciated by those of skill in the art that the dosage may be dependent on the stability of the administered peptide. A less stable peptide may require administration in multiple doses.
- Preparations for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions, and emulsions, which may contain auxiliary agents or excipients which are known in the art.
- Pharmaceutical compositions such as tablets and capsules can also be prepared according to routine methods.
- compositions comprising the peptides of the invention include all compositions wherein the peptide(s) are contained in an amount effective to achieve its intended purpose.
- the pharmaceutical compositions may contain suitable pharmaceutically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically.
- suitable pharmaceutically acceptable vehicles are well known in the art and are described for example in Gennaro, Alfonso, Ed., Remington's Pharmaceutical Sciences, 18th Edition 1990, Mack Publishing Co., Easton, Pa., a standard reference text in this field.
- Pharmaceutically acceptable vehicles can be routinely selected in accordance with the mode of administration and the solubility and stability of the peptides.
- formulations for intravenous administration may include sterile aqueous solutions which may also contain buffers, diluents and other suitable additives.
- Suitable formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form, for example, water-soluble salts.
- suspension of the active compound as appropriate oily injections suspensions may be administered.
- Suitable lipophilic solvents or vehicles include fatty oils, for example, sesame oil, or synthetic fatty acid ester,s for example ethyl oleate or triglycerides.
- Aqueous injection suspensions that may contain substances which increase the viscosity of the suspension include, for example, sodium carboxymethyl cellulose, sorbitol, and/or dextran. optionally, the suspension may also contain stabilizers.
- disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits or into pathological ⁇ -sheet-rich precursors of such deposits to be treated or prevented by administering the pharmaceutical composition of the invention includes, but is not limited to, Alzheimer's disease, FAF, Down's syndrome, other amyloidosis disorders, human prion diseases, such as kuru, Creutzfeldt-Jakob Disease (CJD), Gerstmann-Straussler-Scheinker Syndrome (GSS), prion associated human neurodegenerative diseases as well as animal prion diseases such as scrapie, spongiform encephalopathy, transmissible mink encephalopathy and chronic wasting disease of mule deer and elk.
- human prion diseases such as kuru, Creutzfeldt-Jakob Disease (CJD), Gerstmann-Straussler-Scheinker Syndrome (GSS)
- prion associated human neurodegenerative diseases as well as animal prion diseases such as scrapie,
- the peptides of the invention may also be administered to detect and diagnose the presence or absence of amyloid or amyloid-like deposits in vivo and precursors thereof.
- a designed peptide capable of binding to a hydrophobic ⁇ -sheet forming cluster as a structural determinant in a corresponding amyloid or amyloid-like deposit and precursors thereof, labeled non-radioactively or with a radioisotope, as is well-known in the art, can be administered to a subject for diagnosing the onset or presence of a disease or disorder associated with abnormal protein folding into amyloid or amyloid-like fibril deposits and pathological ⁇ -sheet-rich precursors thereof.
- the binding of such a labeled peptide after administration to amyloid or amyloid-like deposits or precursors thereof can be detected by in vivo imaging techniques known in the art.
- Amyloid deposition appears to be an important factor in the development of neuritic plaque and neuronal disfunction in AD.
- the results of the study presented below indicate that a short peptide partially homologous to the central hydrophobic region of A ⁇ (residues 17-21), but containing amino acids which block the adoption of a ⁇ -sheet structure binds A ⁇ , inhibits amyloid formation in vitro and dissolves preformed A ⁇ fibrils. Furthermore, the inhibitor is able to block the in vivo deposition of AA in the spleen of mice.
- the results of the study support the concept that the formation of a ⁇ -sheet secondary structure is important for fibrillogenesis and it is believed that iA ⁇ inhibits amyloid formation by binding to monomeric A ⁇ peptides thereby blocking the formation of the oligomeric ⁇ -sheet conformation precursor of the fibrils.
- the dissolution of preformed fibrils induced by iA ⁇ may indicate that the monomeric peptide is in equilibrium with the fibrils, as previously suggested (Maggio, J. et al., Proc. Natl. Acad. Sci. USA 89:5461-5466, 1992; Tamaokoa, A. et al., Biochem. Biophys. Res. Commun. 205:834-842, 1994).
- the inhibitor may bind to monomeric peptide, thus displacing the equilibrium, and leading to fibril disaggregation.
- Peptide sequences were determined by automatic Edman degradation on a 477A protein sequencer and the PTH derivatives analyzed with an on-line 120 A PTH analyzer (Applied Biosystems, Foster City, Calif.). Purity of the peptides was evaluated by peptide sequencing and laser desorption mass spectrometry. Stock solutions of the peptides were prepared by dissolving them in 50% acetonitrile. The concentration was determined by amino acid composition analysis on a Waters Pico-Tag amino acid analyzer (Millipore Corp, Bedford, Mass.), after hydrolyzing the samples under reduced pressure in the presence of 6M HCl for 20 hours at 110° C. For experiments, peptide aliquots were lyophilized and resuspended in the buffer used in the assay.
- Electron microscopy For fibril formation, peptides (1 mg/ml) were incubated in 0.1 M Tris-HCl, pH 7.4, for 6 days at room temperature. Samples to be visualized were placed on carbon formvar-coated 300-mesh nickel grids for 1 minute, blotted and stained for 1 minute with 2% uranyl acetate under a vapor of 2% glutaraldehyde and visualized on a Zeiss EM 10 electron microscope (Carl Zeiss, Inc., Thornwood, N.Y.) at 80 kv.
- Circular dichroism studies The secondary structure of A ⁇ and inhibitor peptides was analyzed by circular dichroism in aqueous solution. Spectra were recorded in a Jasco spectropolarimeter Model J-720 (Jasco Inc., Easton, Md.). Aliquots of peptides at a concentration of 0.1-0.2 mg/ml in 20 mM Tris-HCl, pH 7.4, were first centrifuged to produce a clear solution and the spectra were recorded at 1 nm intervals over the wavelength range 190 to 260 nm in a 0.1 cm pathlength cell. Results are expressed in terms of mean residue ellipticity in units of deg cm 2 dmol ⁇ 1 .
- Binding sites The interaction between A ⁇ an iA ⁇ P was studied by fluorescence spectroscopy at 25° C. using a Perkin Elmer model LS50B spectrofluorimeter. 45 ⁇ g of A ⁇ 1-40 was dissolved in 300 ⁇ l of 5 mM Tris, pH 7.4 and immediately the fluorescence spectra was recorded between 290 nm an 400 nm at excitation 280 nm, with slits set at 2.5 nm bandwidth. Different amounts of lyophilized iA ⁇ were added to the A ⁇ solution and after 15 min of incubation the fluorescence spectra was recorded, iA ⁇ at the same concentrations did not give any fluorescence signal above the background.
- the binding of iA ⁇ to A ⁇ was evaluated by the change in fluorescence intensity at 309nm between the spectra of A ⁇ alone and in the presence of different concentrations of the inhibitor.
- the binding data were analyzed with the aid of a curve fitting software (GraphPad Prism version 1.0).
- FIG. 9 an 11 amino acid peptide, called inhibitor of A ⁇ fibrillogenesis peptide (iA ⁇ ) was designed, which has a low probability of adopting a ⁇ -sheet conformation due to the presence of proline residues (FIG. 9).
- Other peptide inhibitors based on the above criteria are shown in FIG. 2A.
- the circular dichroism spectrum of iA ⁇ in aqueous solution was typical of unordered structures (FIG. 10). Samples of iA ⁇ at different concentrations as well as samples incubated for several days have similar spectra (FIG. 10). Indeed, iA ⁇ did not aggregate even at high concentrations (4 mg/ml) or after long periods of incubation (more than 30 days).
- FIG. 12 shows the influence of different concentrations of iA ⁇ on fibrillogenesis of the two major variants of A ⁇ (A ⁇ 1-40 and A ⁇ 1-42).
- iA ⁇ inhibited in a dose-dependent manner in vitro amyloid formation by both A ⁇ variants.
- a ⁇ 1-40 formed only 33.9% and 13.7%, respectively, of the amyloid detectable in the absence of inhibitor (FIG. 12).
- the inhibitor is less efficient with A ⁇ 1-42
- a 5-, 20-, and 40-fold molar excess of iA ⁇ over A ⁇ 1-42 resulted in a 28.7%, 72.3% and 80.6% of inhibition, respectively (FIG. 12).
- Several non-related peptides had no effect on fibrillogenesis or slightly increased A ⁇ amyloid formation, probably by incorporation into the fibrils.
- the 12 residue control peptide did not alter amyloid formation by A ⁇ 1-40 or A ⁇ 1-42 (FIGS. 12 and 13).
- the 15-amino acid peptide designated anti-amyloid peptide 1 (SEQ ID NO: 7) was found to adopt a random coil conformation (FIG. 2B) and was also found to be 90% inhibitory to amyloid fibril formation at 50-fold molar excess over soluble amyloid monomers (FIGS. 5A and 5B).
- FIG. 14A shows the dissolution of A ⁇ 1-40 or A ⁇ 1-42 fibrils after 24 h incubation with different iA ⁇ concentrations.
- the inhibitor efficiently affected disaggregation of A ⁇ 1-40 fibrils, achieving almost complete dissolution when used in a 40-fold molar excess.
- FIG. 14B shows the maximum level of fibril dissolution after 2 days of incubation with iA ⁇ and remained unaltered thereafter.
- Dissolution of preformed fibrils also occurred with the 15 amino acid anti-amyloid peptide 1 (FIGS. 6A and 6B).
- This anti-amyloid peptide also inhibits the fibril formation of other amyloidgenic peptides derived from various other amyloid material, e.g., amyloid-A and the gelsolin related amyloid (FIG. 8).
- Secondary or reactive amyloidosis is an inflammation-associated disorder in which AA protein is deposited in several organs.
- the AA protein is a 76 residues N-terminal fragment derived from proteolysis of a precursor called serum amyloid A (SAA) protein (Levin et al., 1972, supra).
- amyloid-associated proteins bind to A ⁇ in solution and modulate the rate of amyloid formation in vitro (Moore. G. J. Trends Pharmacol. Sci. 15:124-129, 1994; Wisniewski et al., Am. J. Pathol. 145:1030-1035, 1994; Ma et al., Nature 372:92-94, 1994; Snow et al., Neuron. 12:219-234, 1994).
- Amyloid was isolated from mature senile plaque extracted from a brain of a patient who died of Alzheimer's disease. Grey matter was separated from meninges and white matter, cleaned, chopped and homogenized in buffer containing 0.25M sucrose. The homogenate was subjected to a series of centrifugation, treatment with DNase I and collagenase and to a discontinuous sucrose density gradient. After this procedure, pure amyloid cores containing >90% A ⁇ and also several of the amyloid-associated proteins was obtained. 10 ⁇ g of amyloid proteins was incubated for 5 days without and with 200 ⁇ g of iA ⁇ .
- the amount of amyloid was quantitated by using the fluorometric assay based in the binding of thioflavine T to amyloid, as described (Soto, C., et al., J. Biol. Chem. 270: 3063-3067, 1995).
- the material obtained from two different extractions was tested (Samples 1 and 2) and the average and standard error of three different experiments was shown.
- Shorter iA ⁇ derivatives Shorter anti- ⁇ -sheet peptides were designed using peptide iA ⁇ (SEQ ID NO: 8) as a model (Table 3). Two frequent problems associated with peptides used as drugs in medicine, i.e., transport across the blood-brain barrier and generation of an immunoreactive response, can be minimized by shortening the length of the peptide. Studies on the inhibition of A ⁇ amyloid formation in vitro by iA ⁇ derivatives showed that a seven (iA ⁇ 2) and a five (iA ⁇ 4) amino acid residue peptides are similar or better inhibitors than iA ⁇ under the same experimental conditions (Table 3).
- GSS Gerstmann-Straussler-Scheinker
- the peptide 109-141 (SEQ ID NO: 37) as well as the peptide fragments 109-122 (SEQ ID NO: 34) and 106-126 (SEQ ID NO: 35), but not peptide fragment 129-141 (SEQ ID NO: 36), formed typical amyloid fibrils (Zhang H. et al. J. Mol. Biol. 250:514-526, 1995; Gassett, Baldwin, Lloyd, et al.
- the PrP fragment 109-122 (which adopts a ⁇ -sheet conformation) can convert the unstructured fragment 129-141 into a ⁇ -pleated sheet (Nguyen, J., et al. Biochem. 34:4186-4192, 1995).
- the fragments 90-145 and 109-141 are resistant to degradation by proteinase K when they adopt a ⁇ -sheet conformation (Zhang, H., et al. J. Mol. Biol. 250:514-526, 1995).
- the peptide fragment 90-145 which adopts a ⁇ -sheet conformation, can induce the conversion of PrP c into PrP sc in vitro (Kaneko, K. et al., Proc. Natl. Acad. Sci. USA 92:11160-11165, 1995).
- FIG. 21 shows that PrP109-141 converts from a random coil conformation to a ⁇ -sheet structure over time.
- PrP109-141 peptide adopts a ⁇ -sheet conformation, it is highly resistant to degradation by proteinase K (FIG. 22), whereas the same peptide in a random coil structure is highly degradable by this protease.
- FIG. 22 shows aliquots of PrP109-141 were incubated as indicated above for the circular dichroism study for 7 days to obtain a peptide adopting a ⁇ -sheet conformation. The sample was then lyophilized and resuspended in Phosphate buffered saline (PBS).
- PBS Phosphate buffered saline
- FIGS. 23A and 23B show the electron microscopy pattern obtained when PrP109-141 was incubated alone (FIG. 23A) or in the presence of 10-fold molar excess of iPrP-12aa (FIG. 23B), a prototype PrP peptide inhibitor (12 amino acid residues; SEQ ID NO: 24) that was first screened for its ability to inhibit amyloid formation by PrP fragments in vitro. Aliquots of PrP109-141 (2 mg/ml) were incubated for 7 days at 37° C.
- FIG. 24 shows the dose-dependent inhibition of PrP106-126 fibrillogenesis by iPrP-12aa.
- Amyloid formation was quantitated by the fluorometric assay, based on the specific interaction of Thioflavine T (Tht) with amyloid fibrils.
- PrP106-126 at 1 g/ ⁇ l in PBS, pH 7.4, was incubated for 5 days at 37° C., and at the end of the incubation period, 50 mM glycine, pH 9.2, 2 ⁇ M Tht was added in a final volume of 2 ml.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Urology & Nephrology (AREA)
- Neurology (AREA)
- Biophysics (AREA)
- Pathology (AREA)
- Neurosurgery (AREA)
- Immunology (AREA)
- Genetics & Genomics (AREA)
- Toxicology (AREA)
- Hematology (AREA)
- Gastroenterology & Hepatology (AREA)
- Zoology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Analytical Chemistry (AREA)
- Epidemiology (AREA)
- Microbiology (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- General Physics & Mathematics (AREA)
- Physics & Mathematics (AREA)
- Food Science & Technology (AREA)
- Cell Biology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Chemical Kinetics & Catalysis (AREA)
Abstract
Novel peptides capable of interacting with a hydrophobic β-sheet forming cluster of amino acid residues on a protein or peptide for amyloid or amyloid-like deposit formation inhibit and structurally block the abnormal folding of proteins and peptides into amyloid or amyloid-like deposits and into pathological β-sheet-rich conformation as precursors thereof. Methods for preventing, treating or detecting disorders or diseases associated with amyloid-like fibril deposits, such as Alzheimer's disease and prion-related encephalopathies, are also provided.
Description
- The present application is a continuation-in-part of U.S. application Ser. No. 08/630,645, filed Apr. 10, 1996, which is a continuation-in-part of U.S. application Ser. No. 08/478,326, filed Jun. 6, 1995, the entire contents of both of which are hereby incorporated by reference.
- [0002] The U.S. Government has a paid-up license in this invention and the right in limited circumstances to require the patent owner to license others on reasonable terms as provided for by the terms of Grant No. 10953 awarded by National Institutes of Health
- 1. Field of the Invention
- This invention relates to the field of therapeutic peptides for the prevention and treatment of disorders or diseases resulting from abnormal formation of amyloid or amyloid-like deposits, such as, but not limited to, prion-related encephalophathies, Alzheimer's dementia or disease (AD), and other amyloidosis disorders. This invention also relates to the use of the peptides in preventing the formation of or in promoting the redissolution of these insoluble amyloid or amyloid-like deposits.
- 2. Description of the Background Art
- Alzheimer's disease (AD) is the most common form of dementia in adults (C. Soto et al.J. Neurochem. 63:1191-1198, 1994), constituting the fourth leading cause of death in the United States. Approximately 10% of the population over 65 years old is affected by this progressive degenerative disorder that is characterized by memory loss, confusion and a variety of cognitive disabilities. One of the key events in AD is the deposition of amyloid as insoluble fibrous masses (amyloidogenesis) resulting in extracellular neuritic plaques and deposits around the walls of cerebral blood vessels. The main component of amyloid is a 4.1-4.3 kDa hydrophobic peptide, named amyloid β-peptide (Aβ), that is codified in chromosome 21 as part of a much longer amyloid precursor protein APP (Muller-Hill and Beyreuther, Ann. Rev. Biochem. 38:287-307, 1989). The APP starts with a leader sequence (signal peptide), followed by a cysteine-rich region, an acidic-rich domain, a protease inhibitor motif, a putative N-glycosylated region, a transmembrane domain, and finally a small cytoplasmic region. The Aβ sequence begins close to the membrane on the extracellular side and ends within the membrane. Two-thirds of Aβ faces the extracellular space, and the other third is embedded in the membrane (Kang et al. Nature 325:503-507, 1987; Dyrks et al. EMBO J. 7:949-957, 1988). Several lines of evidence suggest that amyloid may play a central role in the early pathogenesis of AD.
- Evidence that amyloid may play an important role in the early pathogenesis of AD comes primarily from studies of individuals affected by the familial form of AD (FAD) or by Down's syndrome. Down's syndrome patients have three copies of APP gene and develop AD neuropathology at an early age (Wisniewski et al.,Ann. Neurol. 17:278-282, 1985). Genetic analysis of families with hereditary AD revealed mutations in chromosome 21, near or within the Aβ sequence (Forsell et al., Neurosci. Lett. 184:90-93, 1995). Moreover, recently it was reported that transgenic mice expressing high levels of human mutant APP progressively develop amyloidosis in brain (Games et al., Nature 373:523-527, 1995). These findings appear to implicate amyloidogenesis in the pathophysiology of AD.
- Recently, the same peptide that forms amyloid deposits in AD brain was also found in a soluble form (sAβ) normally circulating in the human body fluids (Seubert et al.,Nature 359:355-327, 1992; Shoji et al., Science 258:126-129, 1992). Zlokovic et al., Biochem. Biophys. Res. Commun. 205:1431-1437 (1994), reported that the blood-brain barrier (BBB) has the capability to control cerebrovascular sequestration and transport of circulating sAβ, and that the transport of the sAβ across the BBB was significantly increased when sAβ was perfused in guinea pigs as a complex with apolipoprotein J (apoJ). The sAβ-apoJ was found in normal cerebrospinal fluid (CSF; Ghiso et al. Biochem. J. 293:27-30, 1994) and in vivo studies indicated that sAβ is transported with apoJ as a component of the high density lipoproteins (HDL) in normal human plasma (Koudinov et al., Biochem. Biophys. Res. Commun. 205:1164-1171, 1994). It was also recently reported by Zlokovic et al., Proc. Natl. Acad. Sci. USA 93:4229-04233 (1996), that the transport of sAβ across the BBB was almost abolished when the apoJ receptor gp330 was blocked. It is believed that the conversion of sAβ to insoluble fibrils is initiated by a conformational or proteolytic modification of the 2-3 amino acid longer soluble form. It has been suggested that the amyloid formation is a nucleation-dependent phenomena in which the initial insoluble “seed” allows the selective deposition of amyloid (Jarrett et al., Biochem. 32 :4693-4697, 1993).
- Peptides containing the sequence 1-40 or 1-42 of Aβ and shorter derivatives can form amyloid-like fibrils in the absence of other protein (Soto et al.,J. Neurochem. 63:1191-1198, 1994), suggesting that the potential to form amyloid resides mainly in the structure of Aβ. The relation between the primary structure of Aβ and its ability to form amyloid-like fibrils was analyzed by altering the sequence of the peptide. Substitution of hydrophilic residues for hydrophobic ones in the internal Aβ hydrophobic regions (amino acids 17-21) impaired fibril formation (Hilbich et al., J. Mol. Biol. 228:460-473, 1992), suggesting that Aβ assembly is partially driven by hydrophobic interactions. Indeed, larger Aβ peptides (Aβ1-42/43) comprising two or three additional hydrophobic C-terminal residues are more amyloidogenic (Jarrett et al., Biochem 32:4693-4697, 1993). Secondly, the conformation adopted by Aβ peptides is crucial in amyloid formation. Aβ incubated at different pH, concentrations and solvents has mainly an α-helical (random coil) or a β-sheet secondary structure (Barrow et al., J. Mol. Biol. 225:1075-1093, 1992: Burdick et al., J. Biol. Chem. 267:546-554, 1992; Zagorski et al., Biochem. 31:5621-5631, 1992). The Aβ peptide with α-helical or random coil structure aggregates slowly; Aβ with β-sheet conformation aggregates rapidly (Zagorski et al., Biochem. 31:5621-5631, 1992; Soto et al., J. Biol. Chem. 270:3063-3067, 1995; Soto and Castano, Biochem. J. 314:701-707, 1.996). The importance of hydrophobicity and β-sheet secondary structure on amyloid formation also is suggested by comparison of the sequence of other amyloidogenic proteins.
- Analysis of Aβ aggregation by turbidity measurements indicates that the length of the C-terminal domain of Aβ influences the rate of Aβ assembly by accelerating nucleus formation (Jarrett et al.,Cell 73:1055-1058, 1993 ). Thus, the C-terminal domain of Aβ may regulate fibrillogenesis. However, in vitro modulators of Aβ amyloid formation, such as metal cations (Zn, Al) (Bush et al., Science 265:1464-1467, 1994; Exley et al., FEBS Lett. 324:293-295, 1993) heparin sulfate proteoglycans, and apoliprotein E (Strittmatter et al., Proc. Natl. Acad. Sci. USA 90:1977-1981, 1993) interact with the 12-28 region of Aβ. Moreover, mutations in the βPP gene within the N-terminal Aβ domain yield analogs more fibrillogenic (Soto et al., 1995, supra; Wisniewski et al., Biochem. Biophys. Res. Commun. 179:1247-1254, 1991). Finally, while the C-terminal domain of Aβ invariably adopts a β-strand structure in aqueous solutions, environmental parameters determine the existence of alternative conformation in the Aβ N-terminal domain (Barrow et al., 1992, supra; Soto et al., 1995, supra; Burdick et al., 1992, supra). Therefore, the N-terminus may be a potential target site for inhibition of the initial random coil to β-sheet conformational change.
- The emerging picture from studies with synthetic peptides is that Aβ amyloid formation is dependent on hydrophobic interactions of Aβ peptides adopting an antiparallel β-sheet conformation and that both the N- and C-terminal domains are important for amyloid formation. The basic unit of fibril formation appears to be the conformer adopting an antiparallel β-sheet composed of strands involving the regions 10-24 and 29-40/42 of the peptide (Soto et al., 1994, supra). Amyloid formation proceeds by intermolecular interactions between the β-strands of several monomers to form an oligomeric β-sheet structure precursor of the fibrillar62 -cross conformation. Wood et al., Biochemistry 34:724-730 (1995), reported the insertion of aggregation-blocking prolines into amyliod proteins and peptides, as exemplified by test peptides having the amino acid sequences of SEQ ID NOs: 50-65, to prevent aggregation of such proteins and peptides. In this manner, the authors suggest that novel proteins can be designed to avoid the problem of aggregation as a barrier to their production without affecting the structure or function of the native protein. Thus, Wood et al. seek to produce novel proteins that would not aggregate during recombinant protein production and purification by inserting aggregation-blocking prolines into these novel prolines. The inhibitory peptides of the present invention, which inhibit the formation of amyloid deposits from native Aβ as opposed to solely preventing aggregation of a proline-modified modified peptide or protein, are not intended to include the peptides of Wood et al. having the amino acid sequences SEQ ID NOs: 50-65.
- To date there is no cure or treatment for AD and even the unequivocal diagnosis of AD can only be made after postmortem examination of brain tissues for the hallmark neurofibrillary tangles (NFT) and neuritic plaques. However, there are several recent publications outlining strategies for the treatment of Alzheimer's disease.
- Heparin sulfate (glycosoaminoglycan) or the heparin sulfate proteoglycan, perlecan, has been identified as a component of all amyloids and has also been implicated in the earliest stages of inflammation-associated amyloid induction. Kisilevsky et al.,Nature Medicine 1(2):143-148, (1995) describes the use of low molecular weight (135-1,000 Da) anionic sulfonate or sulfate compounds that interfere with the interaction of heparin sulfate with the inflammation-associated amyloid precursor and the β-peptide of AD. Heparin sulfate specifically influences the soluble amyloid precursor (SAA2) to adopt an increased β-sheet structure characteristic of the protein-folding pattern of amyloids. These anionic sulfonate or sulfate compounds were shown to inhibit heparin-accelerated Alzheimer's Aβ fibril formation and were able to disassemble preformed fibrils in vitro as monitored by electron micrography. Moreover, when administered orally at relatively high concentrations (20 or 50 mM), these compounds substantially arrested murine splenic inflammation-associated amyloid progression in vivo in acute and chronic models. However, the most potent compound, poly-(vinylsulfonate), was acutely toxic.
-
Anthracycline 4′-iodo-4′-deoxy-doxorubicin (IDOX) has been observed clinically to induce amyloid resorption in patients with immunoglobin light chain amyloidosis (AL). Merlini et al., Proc. Natl. Acad. Sci. USA 92:2959-2963 (1995), elucidated its mechanism of action. IDOX was found to bind strongly via hydrophobic interactions to two distinct binding sites (Scatchard analysis) in five different tested amyloid fibrils, inhibiting fibrillogenesis and the subsequent formation of amyloid deposits in vitro. Preincubation of IDOX with amyloid enhancing factor (AEF) also reduced the formation of amyloid deposits. Specific targeting of IDOX to amyloid deposits in vivo was confirmed in an acute murine model. This binding is distinct from heparin sulfate binding as removal of the glycosaminoglycans from extracted amyloid fibrils with heparinases did not modify IDOX binding. The common structural feature of all amyloids is a β-pleated sheet conformation. However, IDOX does not bind native amyloid precursor light chains which suggests that the β-pleated sheet backbone alone is not sufficient to form the optimal structure for IDOX binding, and that it is the fibril cross-β-sheet quaternary structure that is required for maximal IDOX binding. It has been found that the amount of IDOX extracted from spleens is correlated with amyloid load and not circulating serum precursor amyloid levels. IDOX, however, is also extremely toxic. - The regulation and processing of amyloid precursor protein (APP) via inhibition or modulation of phosphorylation of APP control proteins has also been investigated in U.S. Pat. No. 5,385,915 and WO 9427603. Modulating proteolytic processing of APP to nucleating forms of AD has also been examined in AU 9338358 and EP569777. WO 95046477 discloses synthetic peptides of composition X-X-N-X (SEQ ID NO: 69) coupled to a carrier, where X is a cationic amino acid and N is a neutral amino acid, which inhibit Aβ binding to glycosoaminoglycan. Peptides containing Alzheimer's Aβ sequences that inhibit the coupling of α-1-antichymotrypsin and Aβ are disclosed in WO 9203474.
- Prions are the infectious particles responsible for a group of fatal neurodegenerative diseases known as spongiform encephalopathies (for reviews, see Prusiner & DeArmond,Annu. Rev. Neurosci. 17:311-339, 1994; Prusiner, Science 252:1515-1522, 1991). Creutzfeldt-Jakob disease (CJD), kuru, Gerstmann-Straussler syndrome (GSS) and fatal familial insomnia are all human neurodegenerative diseases caused by prions and are frequently transmissible to laboratory animals. Familial CJD and GSS are also genetic disorders. In addition to the prion diseases in humans, four disorders of animals are included in this type of disease. Scrapie in sheep and goats is the most common of the prion diseases. Bovine spongiform encephalopathy (BSE), also known as the “mad cow disease”, transmissible mink encephalopathy, and chronic wasting disease of captive mule deer and elk are all thought to result from the ingestion of scrapie-infected animal products.
- To date there is no cure or effective treatment for prion-related diseases. The infectious agent causing prion-related diseases differ from bacteria, fungi, parasites, viroids and viruses in that no DNA is needed and it apparently only consists of protein. The principal component of prions is the glycoprotein called PrPsc. Prion replication is hypothesized to occur when PrPsc in the infecting inoculum interacts specifically with host PrPc (normal cellular PrP isoform), catalyzing its conversion to the pathogenic form of the protein (Cohen, F. E. et al., Science 264:530-531, 1994). It is postulated that this conversion takes place spontaneously in PrP molecules carrying mutations that have been linked to familial forms of prion disease.
- The cellular prion protein (PrPc) is a sialoglycoprotein encoded by a gene that in humans is located on chromosome 20 (Oesch, B. et al., Cell 40:735-746, (1985); Basler, K. et al., 46:417-428 (1986); Liao, Y. J. et al., Science 233:364-367 (1986); Meyer, R. K. et al., Proc. Natl. Acad. Sci. USA 83:2310-2314 (1986); Sparkes, R. S. et al., Proc. Natl. Acad. Sci. USA 83:7358-7362 (1986); Bendheim, P. E. et al. J. Infect. Dis. 158:1198-1208 (1988); Turk, E. et al. Eur. J. Biochem. 176:21-30 (1988)). The PrP gene is expressed in neural and non-neural tissues, the highest concentration of mRNA being in neurons (Chesebro, B. et al., Nature 315:331-333 (1985); Kretzschmar, H. A. et al., Am. J. Pathol. 122:1-5 (1986); Brown, H. R. et al., Acta Neuropathol. 80:1-6 (1990); Cashman, N. R. et al., Cell 61:185-192 (1990); Bendheim, P. E., Neurology 42:149-156 (1992)).
- The translation product of the PrP gene consists of 253 amino acids in humans (Kretzschmar, H. A. et al.,DNA 5:315-324 (1986); Pucket, C. et al., Am. J. Hum. 49:320-329 (1991)), 254 in hamster and mice or 256 amino acids in sheep and undergoes several post-translational modifications. In hamsters, a signal peptide of 22 amino acids is cleaved at the N-terminus, 23 amino acids are removed from the C-terminus on addition of a glycosyl phosphatidylinositol (GPI) anchor, and asparagine-linked oligosaccharides are attached to residues 181 and 197 in a loop formed by a disulfide bond (Turk, E. et al., Eur. J. Biochem. 176:21-30 (1988); Hope, J. et al., EMBO J. 5:2591-2597 (1986); Stahl, N. et al., Cell 51:229-240 (1987); Stahl, N. et al., Biochemistry 29:5405-5412 (1990); Safar, J. et al., Proc. Natl. Acad. Sci. USA 87:6377 (1990)).
- In prion-related encephalopathies, PrPc (normal cellular isoform) is converted into an altered form designated PrPSc, that can be experimentally distinguished from PrPc by the following three properties (Cohen et al. Science 264:530-531 (1994): (1) PrPsc is insoluble in physiological solvents and forms aggregates; (2) PrPsc is partially resistant to proteolytic degradation by proteinase K in that only the N-terminal 67 amino acids are removed by proteinase K digestion under conditions in which prPc is completely degraded, and which results in a N-terminally truncated form known as PrP27-30; and (3) PrPsc has an alteration in protein conformation from α-helical for PrPc to an altered form which is rich in β-sheet secondary structure.
- Several lines of evidence indicate that PrPsc is a major and necessary component of the infectious prion (reviewed in Prusiner, S. B. Science 252:1515-1522, 1991) and are as follows: (a) copurification of PrP27-30 and scrapie infectivity were determined by biochemical methods where the concentration of PrP27-30 is proportional to prion titer; (b) kinetics of proteolytic digestion of PrP27-30 and infectivity are similar; (c) copurification of PrPsc and infectivity were observed using immunoaffinity; (d) infectivity was neutralized by anti-PrP antibodies; (e) detection of PrPsc were only detected in clones of cultured cells producing infectivity; (f) most, if not all, of the familial cases of PrP-related disorders are linked to mutations in the PrP gene; (g) mice expressing PrP genes with point mutations linked to GSS spontaneously develop neurologic dysfunction, spongiform brain degeneration and astrocytic gliosis; (h) the species barrier to prion transmission from hamster to mouse could be overcome by introducing a Syriam hamster PrP transgene into the recipient mouse line; and (i) mice devoid of PrP gene are resistant to scrapie infection, developing neither symptoms of scrapie nor allowing propagation of the infectious agent. It has also been established that the protease-resistant core of PrPsc is the major structural protein of amyloid fibrils that accumulate intracerebrally in some of these conditions (Brendheim, P. E. et al., Nature 310:418-421 (1984); DeArmond, S. J. et al., Cell 41:221-235 (1985); Kitamoto, T. et al., Ann. Neurol. 20:204-208 (1986); Robert, G. W. et al., N. Engl. Med. 315:1231-1233 (1986); Ghetti, B. et al., Neurology 39:1453-1461 (1989); Tagliavini, F. et al., EMBO J. 10:513-519 (1991); Kitamoto, T. et al., Neurology 41:306-310 (1991)).
- Although there are obvious differences in the etiology and pathogenesis of PrP-related diseases and Alzheimer's disease (AD), a remarkable number of similarities exist (for reviews, see Kelly, J. W.Curr. Opin. Struct. Biol. 6:11-17, 1996; Castano, E. M. & Frangione, B. Curr. Opin. Neurol. 8:279-285, 1995; Diringer, H. Exp. Clin. Immunogenet. 9:212-229, 1992; DeArmond, S. J. Curr. Opin. Neurol. 6:872-881, 1993), namely: (a) the clinical symptoms of both diseases are similar, including memory loss, behavioral abnormalities, cognitive problems and dementia; (b) both disorders are characterized clinically by age-related sporadic and familial forms of the disease; (c) an abnormal form of a neuronal membrane protein (Amyloid-β precursor protein and PrP) appears to play a key role in the pathogenesis of both diseases; (d) both Aβ and PrP are amyloidogenic and neurotoxic; (e) an important part of the cases affected by familial prion disease typically develop neuritic plaques similar to the AD plaques, but containing PrP (instead of Aβ) amyloid cores; (f) a hallmark event in both diseases is the conformational transition from an α-helical-random coil structure to a β-sheet conformation in either PrP or Aβ.
- While amyloid deposition is not a general characteristic of PrP-related diseases, extensive evidence suggests that the disorder is caused by a disease-specific posttranslational modification of a normal protein isoform (cellular PrP or PrPc) which results in the abnormal scrapie PrP (PrPsc) (Prusiner, S. B. Science 252:1515-1522, 1991). Chemical differences have not been detected between the two PrP isoforms; they only differ in their conformations. For instance, the major secondary structure of PrPsc is β-pleated sheet, as opposed to the predominance of α-helix in PrPc (Pan, K. M. et al. Proc. Natl. Acad. Sci. (USA) 90:10962-10966, 1993). As discussed above, while amyloid or amyloid-like deposits are not observed in all subjects with a PrP-related disease, the pathological β-sheet-rich conformation of PrPsc as an abnormal precursor of amyloid or amyloid-like deposits however are always present.
- Citation of any document herein is not intended as an admission that such document is pertinent prior art, or considered material to the patentability of any claim of the present application. Any statement as to content or a date of any document is based on the information available to applicant at the time of filing and does not constitute an admission as to the correctness of such a statement.
- The present invention relates to novel inhibitory peptides capable of interacting or binding to a hydrophobic β-sheet forming cluster on a protein or peptide which forms amyloid or amyloid-like deposits so as to inhibit or structurally block the abnormal folding of the protein or peptide into a pathological β-sheet structure to form an amyloid or amyloid-like deposit, or a precursor thereof, such as is observed in Alzheimer's disease, amyloidosis disorders, prion-related encephalophathies, etc. The peptide includes a hydrophobic portion having one or more β-sheet blocking amino acid residues, and may also include charged amino acids at one or both ends of the peptide. Such inhibitory peptides have a low probability of adopting a β-sheet conformation and are capable of associating with said hydrophobic β-sheet forming cluster on the protein or peptide to structurally block and inhibit the abnormal folding thereof into amyloid or amyloid-like deposits, or pathological β-sheet precursors of amyloid or amyloid-like deposits.
- The present invention also relates to a method of preventing or treating a disorder or disease associated with the formation of amyloid or amyloid-like deposits involving the abnormal folding of a protein or peptide having a hydrophobic β-sheet forming cluster into a β-sheet structure, by administering an effective amount of such an inhibitory peptide to a subject in need thereof to prevent or reverse the abnormal folding of the protein or peptide into amyloid or amyloid-like deposits or pathological β-sheet precursors thereof.
- The present invention further relates to pharmaceutical compositions for the prevention or therapeutic treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits and pathological β-sheet-rich precursors thereof, using such inhibitory peptides.
- The present invention also relates to a method for detecting disorders or diseases associated with amyloid or amyloid-like fibril deposits and pathological β-sheet-rich precursors thereof.
- FIGS.1A-B provide a consensus sequence for amyloidogenesis in terms of hydrophobicity and secondary structure properties. FIG. 1A is the primary structure of the amyloidogenic sequence of peptides involved in the formation of several amyloid deposits. The sequences correspond to: amyloid β-peptide (SEQ ID NO: 1) found in Alzheimer's disease, its Dutch variant and Downs Syndrome; amyloid A (SEQ ID NO: 2) found in secondary amyloidosis and familial Mediterranean fever; gelsolin amyloid (SEQ ID NO: 3) related to familial amyloidosis of Finnish type; amyloid L (SEQ ID NO: 4) found in immunoglobulin-related primary amyloidosis; β2-microglobulin amyloid (SEQ ID NO: 5) found in patients with chronic hemodialysis-related amyloidosis; and apolipoprotein A1 amyloid (SEQ ID NO: 6) related to familial amyloidotic polyneuropathy. Amino acids written in bold correspond to hydrophobic residues and those underlined represent positions with mutation related to the hereditary form of the disease. FIG. 1B provides the β-sheet prediction for the 15 amino acid fragments containing the sequences shown in FIG. 1A. The solid bar represents regions with a high probability of adopting a β-sheet structure.
- FIGS.2A-B provide the amino acid sequence for several anti-amyloid peptides. FIG. 2A shows the amino acid sequences four anti-amyloid peptides labeled as anti-amyloid 1 (SEQ ID NO: 7), anti-amyloid 2 (SEQ ID NO: 8), anti-amyloid 3 (SEQ ID NO: 9) and anti-amyloid 4 (SEQ ID NO: 10). Hydro-phobic amino acids are highlighted in bold. FIG. 2B shows the circular dichroism spectrum of the anti-amyloid peptide 1 (SEQ ID NO: 7) recorded as described in Example 1.
- FIG. 3 is a schematic representation of the β-cross conformation for amyloid fibrils showing the crucial importance of the interactions by hydrogen bonding between the monomeric β-strand to form the intermolecular β-cross structure.
- FIGS.4A-B show the effect of
anti-amyloid peptide 2 having the sequence of SEQ ID NO: 8 on the amyloid formation by Aβ in vitro. Amyloid formation was quantitated by the fluorometric assay described in Example 1. FIG. 4A shows the dose-dependent inhibition of amyloidogenesis, using anti-amyloid peptide 2 (shown as filled squares) and a 12 amino acid-non related peptide as a control (shown as unfilled square). The incubation time was 24 hours at room temperature and the Aβ concentration was 1 mg/ml in 0.1 M Tris, pH 7.4. FIG. 4B shows the effect of anti-amyloid peptide 2 (SEQ ID NO: 8) on the amyloid formation after various incubation times. - The inhibitory effect of the peptide remained unaltered over several days of incubation. Incubations containing Aβ, alone, are depicted by unfilled squares; incubations of Aβ, and a control peptide are depicted by unfilled circles; and incubations of Aβ and
anti-amyloid peptide 2 are depicted by filled squares. The Aβ concentration used was 1 mg/ml incubated in a molar ratio ofanti-amyloid peptide 2 or control peptide of 1:20. Neither theanti-amyloid peptide 2 nor the control peptide gave fluorescence values over the background level of 1-2 fluorescence units. - FIGS.5A-C show electron micrographs of negative-stained preparations of Aβ (FIG. 5A), Aβ incubated with anti-amyloid peptide 1 (SEQ ID NO: 7: FIG. 5B) and
anti-amyloid peptide 1 alone (FIG. 5C). Aliquots of Aβ were incubated at 1 mg/ml with or without theanti-amyloid peptide 1 in a molar ratio 1:50 (Aβ:anti-amyloid) for 6 days at room temperature. - FIGS.6A-B show the effects of
anti-amyloid peptide 1 on the redissolution of preformed fibrils. Amyloid fibrils were formed by incubating Aβ (1 mg/ml) for 3 days at room temperature.Anti-amyloid peptide 1 was then added in a molar ratio 1:50 (Aβ:anti-amyloid peptide 1). The incubation was continued for 15 minutes, 6 hours or 24 hours and the amyloid formation was quantitated by the fluorometric assay (FIG. 6A). Fluorescence values represent the amount of amyloid formed. FIG. 6B provides electron micrographs of the nonincubated (left side picture) and incubated fibrils for 24 hours with anti-amyloid peptide 1 (right side picture). Magnification is 50,000×. - FIGS.7A-C show the physio-chemical characterization of the amphoterin (HMG-1) derived amyloid fragment, ATNp. FIG. 7A provides the amino acid sequence of the fragment ATNp (SEQ ID NO: 11). Hydrophobic amino acid residues are highlighted in bold. FIG. 7B shows the Chou-Fasman prediction for β-sheet structure of ATNp. The sequence with the highest β-sheet structure probability is indicated with a bar. FIG. 7C is an electron micrograph of negative-stained preparations of ATNp with formed amyloid-like fibrils.
- FIG. 8 is a bar graph showing the effect of
anti-amyloid peptide 1 on the amyloid formation by Aβ and of peptides derived from the amyloidogenic sequence of gelsolin amyloid and amyloid A. Either Aβ or the fifteen amino acid peptides containing the amyloidogenic sequence of gelsolin amyloid (SEQ ID NO: 12) and amyloid A (SEQ ID NO: 13) were incubated in a concentration of 1 mg/ml for 24 hours without and withanti-amyloid peptide 1 in a molar ratio of 1:5 or 1:20. - FIG. 9 shows the structural characteristics of anti-amyloid peptide 2(iAβ). The amino acid sequence and β-sheet probability for iAβ (SEQ ID NO: 8) and for the region of Aβ (SEQ ID NO: 14) used as a template for iAβ is shown underneath the β-sheet probability profile where the solid bar represents the region of Aβ having a high probability of β-sheet structure.
- FIG. 10 shows the circular dichroism spectra of iAβ at different peptide concentration.
- FIG. 11 shows the Aβ-iAβ interaction as quantitated by the quenching of the intrinsic fluorescence of Aβ (tyrosine 10) induced by the binding of iAβ. The inset shows the fluorescence spectra of Aβ incubated alone or in the presence of 4 μM iAβ.
- FIG. 12 shows the dose-dependent inhibition of Aβ1-40 and Aβ1-42 fibrillogenesis by iAβ. Amyloid formation was quantitated by the fluorometric assay, as described in Example 1. The Aβ concentration was 1 mg/ml in 0.1M Tris, pH 7.6 and an incubation time of 24 h.
- FIG. 13 shows the effect of iAβ on amyloid formation by Aβ1-40, after different incubation periods. The molar ratio Aβ:iAβ (or control) was 1:20;
Aβ concentration 1 mg/ml. Amyloid formation was quantitated as in FIG. 12. iAβ or the control peptide alone did not give fluorescence values above the background level. - FIGS. 14A and 14B shows the dissolution of preformed Aβ fibrils by iAβ in vitro. Amyloid fibrils were first preformed by incubating Aβ1-40 or Aβ1-42 at a concentration of 1 mg/ml for 6 days at room temperature. Fluorometric quantitation of amyloid as described in Example 1. FIG. 14A shows the effect of different molar ratios of iAβ or control peptide on fibril disassembly after 24 h of incubation. FIG. 14B fibril dissolution induced by a 40-fold molar excess of iAβ or control peptide after different incubation periods at room temperature.
- FIGS. 15a-f shows the electron microscopy analysis of the effect of iAβ on fibril formation and dissolution. Aliquots of Aβ1-40 (2 mg/ml) were incubated at 37° C. with or without iAβ or control peptide at a molar ratio 1:40 (Aβ:iAβ), centrifuged and the pellet loaded on electron microscopy grids, stained and visualized as described in the Materials and Methods. FIG. 15a shows Aβ incubated for 6 days; FIG. 15b shows Aβ incubated with iAβ for 6 days; FIG. 15c shows Aβ incubated alone for 5 days and then for 1 day with iAβ; FIG. 15d shows iAβ incubated for 6 days at the same concentration as in FIGS. 15b and c; FIG. 15e shows Aβ incubated with the control peptide for 6 days; and FIG. 15f shows control peptide incubated alone for 6 days at the same concentration used in FIG. 15e.
- FIG. 16 shows the inhibition of amyloid formation after long period of incubation (days) in the presence of low concentrations of iAβ. 30 μg of Aβ1-42 was incubated in 30 μl of 0.1M tris, pH 7.4 with a molar ratio 1:5 (Aβ:iAβ) of the inhibitor for different times at room temperature. Amyloid was quantitated by the thioflavine T fluorometric assay and expressed as a percentage of the amount of amyloid incubated for the same time in the absence of the inhibitor.
- FIG. 17 shows the inhibition of Aβ fibrillogenesis by iAβ containing all D-amino acids.
- FIG. 18 shows the effect of iAβ on the promotion of Aβ fibrillogenesis induced by apolipoprotein E. 30 μg of Aβ1-40 were incubated with or without 2.4 μg of human plasma apolipoprotein E (apoE). Samples of Aβ alone or Aβ/apoE were incubated also with 1:10 (Aβ:iAβ) of the inhibitor. All the incubations were performed for 24 h at room temperature. Amyloid formation was evaluated by the thioflavine T fluorometric assay. The average of two different experiments is shown.
- FIG. 19 shows Alzheimer's amyloid plaque dissolution by iAβ.
- FIG. 20 shows the effect of iAβ on the Aβ-induced cell toxicity.
- FIG. 21 shows the change in the conformation of the PrP 109-141 fragment as evaluated by circular dichroism at time points of 0, 1, 3, 5, 7 and 10 days.
- FIG. 22 shows samples of the PrP 109-141 fragment in a random coil or β-sheet conformation being treated with proteinase K and electrophoresed on SDS polyacrylamide gel. Arrows on the left indicate the position of molecular weight standards.
- FIGS. 23A and 23B show the effect of the presence (FIG. 23B) or absence (FIG. 23A) of peptide iPrP-12aa on PrP109-141 fibrillogenesis as evaluated by electron microscopy.
- FIG. 24 shows the dose-dependent inhibition of PrP106-126 peptide fibrillogenesis by iPrP-12aa. The control peptide is CP1 (SEQ ID NO: 49).
- FIG. 25 shows the influence of iPrP-12aa on proteinase K degradation of PrP109-141 as determined by SDS-PAGE. Aliquots of PrP109-141 were converted from random coil to β-sheet by incubation for 7 days under the conditions described in Example 2 for the circular dichroism study in the absence (lane 3) or in the presence of 10-fold molar excess of an unrelated control peptide (CP1) (lane 4) or iPrP-12aa (lane 5). The sample was then lyophilized and resuspended in PBS. A similar aliquot of the fragment that was not pre-incubated (adopting a random coil conformation) was also lyophilized and resuspended in PBS (lane 2). The samples were treated with proteinase K (1:400 w/w) for 60 min. The reactions were then stopped and the samples analyzed by electrophoresis as described above for the results shown in FIG. 22.
Lane 1 corresponds to molecular weight standards. - FIG. 26 shows the inhibition of PrP109-141 conformational transition with inhibitor peptide iPrP-12aa as evaluated by circular dichroism at t=0 and t=7 days.
- Novel peptides specifically designed to interfere with the β-sheet conformation of precursor proteins or peptides involved in the formation of amyloid or amyloid-like deposits have been developed. The present invention is directed to these novel peptides, pharmaceutical compositions containing one or a mixture of such peptides of the invention, and methods for preventing, treating, or detecting disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits or precursors thereof having a pathological β-sheet structure.
- It has now been found that, while the amino acid sequence of proteins or peptides from different amyloid or amyloid-like deposits, or pathological precursors thereof, differ, all of these amyloidogenic proteins or peptides contain a segment having the common characteristic of a hydrophobic β-sheet forming cluster of amino acids (mainly phenylalanine, valine, alanine, leucine, and isoleucine) being present within a larger segment strongly predicted to have a β-sheet conformation (FIGS. 1A and 1B). The hydrophobic β-sheet forming cluster is believed to determine the binding of protein or peptide monomers resulting in aggregation, whereas the β-sheet potential of the longer sequence, of which the hydrophobic β-sheet forming cluster is a part, is believed to control the ordering of the aggregates into a β-cross conformation (β-cross quaternary fibril structure) typical of amyloid fibril structure (FIG. 3). Even a non-amyloid related peptide, which contains a potential amyloidogenic sequence motif (FIGS. 7A and 7B) such as obtained by proteolysis of amphoterin, forms typical amyloid-like fibrils in vitro (FIG. 7C).
- The novel peptides of the present invention contain a hydrophobic portion or segment of at least three amino acid residues, where this portion is interrupted by one or more β-sheet blocking amino acid residues without substantially changing the hydrophobicity of the portion. In addition, these novel peptides can contain more than three hydrophobic amino acid residues within this portion, and/or contain other amino acid residues within this cluster or outside of it that also act to lower the propensity of the peptides of the present invention to adopt a β-sheet conformation.
- Preferably, the peptides capable of interacting or binding with a structural determinant having a hydrophobic β-sheet forming cluster of amino acid residues on a protein or peptide involved in amyloid or amyloid-like deposit formation, which inhibits the abnormal folding of such a protein or peptide, are designed with a knowledge of the structural determinants for amyloid, amyloid-like deposits, or pathological β-sheet precursor formation by prediction of a hydrophobic β-sheet forming cluster and/or by experimental confirmation of β-sheet conformation. However, prior identification of the structural determinant is not always necessary.
- Peptides having a hydrophobic β-sheet blocking portion which interacts with a hydrophobic β-sheet forming determinant of the protein or peptide, but with a very low probability of adopting a β-sheet conformation themselves, are designed to bind to the structural determinant and to function as an inhibitor of the conformational change resulting in the pathological β-sheet rich precursors of amyloid fibril formation and/or as an agent that dissolves preformed amyloid fibrils. In addition, one or more charged amino acid residue, such as aspartic acid, glutamic acid, arginine, or lysine, can be placed at one or both ends of the peptide to increase the solubility of the inhibitory peptide.
- Furthermore, the inhibitory peptides of the invention contain one or more β-sheet blocking amino acids, such as Pro, Gly, Asn, or His, either within the hydrophobic portion containing at least three amino acid residues or immediately adjacent to this portion so as to prevent the binding of protein or peptide monomers into aggregates and the ordering of such aggregates into an altered conformation such as the β-cross conformation typical of amyloid fibril structure. While the peptides can be designed to be preferably homologous or partially homologous to the hydrophobic β-sheet forming cluster as the structural determinant they are to interact with, amino acid homology is not absolutely required as long as the peptide has a portion of sufficient hydrophobicity so that it will interact strongly with the hydrophobic β-sheet forming cluster to structurally block abnormal protein or peptide folding into fibril deposits or pathological β-sheet-rich precursors thereof.
- In the design of the inhibitory peptides of the present invention, it is important not only to have a hydrophobic portion or cluster that can interact and bind to the hydrophobic β-sheet forming cluster of the amyloidogenic protein or peptide, but also to introduce one or more β-sheet blocking amino acid residues. Thus, whereas the hydrophobicity of the inhibitory peptide facilitates the binding interaction with the amyloidogenic protein or peptide, the presence of one or more β-sheet blocking amino acid residues, located in the hydrophobic portion or immediately adjacent to it, lowers the β-sheet forming potential of the inhibitory peptide and inhibits the conformational transition of the amyloidogenic protein or peptide into a β-sheet structure found to be formed in amyloid or amyloid-like deposits and pathological β-sheet precursors thereof.
- As a general non-limiting example of a preferred design approach, which was used for some of the inhibitory peptides of the present invention (such as some of the peptides of Table 1), a peptide is designed so that a hydrophobic portion of at least three amino acids is homologous to the hydrophobic β-sheet forming cluster predicted or identified experimentally to be involved in abnormal protein folding into a β-sheet structure. Highly hydrophobic amino acid residues of the hydrophobic β-sheet forming cluster are generally incorporated into the sequence of the homologous hydrophobic portion of the inhibitory peptide. In addition, any non-hydrophobic or poorly hydrophobic amino acid residues in the hydrophobic β-sheet forming cluster can be incorporated into the homologous hydrophobic portion, or deleted, or replaced with another amino acid such as a β-sheet blocking residue, preferably proline.
- It is intended that the homologous hydrophobic portion of the inhibitory peptide has one or more β-sheet blocking residues that interrupt the homology to the hydrophobic β-sheet forming cluster by avoiding the presence of more than three contiguous amino acids within the homologous hydrophobic portion which are 100% homologous to the corresponding contiguous amino acids in the hydrophobic β-sheet forming cluster. In this manner, the propensity or potential for forming a β-sheet conformation is dramatically reduced for the hydrophobic portion and for the inhibitory peptide as a whole, while the degree of hydrophobicity of the hydrophobic portion is kept substantially unchanged from that of the hydrophobic β-sheet forming cluster. This provides for the capability of the inhibitory peptide to hydrophobically interact/bind with the amyloidogenic protein or peptide where the β-sheet blocking capability of the designed inhibitory peptide is allowed to manifest itself by inhibiting the formation of β-sheet structures characteristic of amyloid or amyloid-like deposits and precursors thereof.
- An additional design parameter that is to be considered is the addition of charged amino acid residues at one or both ends of the inhibitory peptide which act mainly to increase the solubility of the peptide in an aqueous medium. This feature is more important with longer peptides and while preferred, is not absolutely necessary in short peptides.
- It will be appreciated that those of skill in the art can easily synthesize an array of inhibitory peptides, designed in accordance with the present invention, that can be readily tested using the methods described in Examples 1 and 2 for Aβ and PrP, respectively, for the ability to inhibit the conformational transition of amyloidogenic proteins or peptides into pathological β-sheet structures as precursors to, or as fibrils of, amyloid or amyloid-like deposits.
- Prion protein PrP normally assumes an a-helical conformation, but abnormal protein folding alters the normal PrP conformation to an abnormal β-sheet conformation. Considering the similarities between PrP-related disorders and Alzheimer's disease, and since the acquisition of a β-sheet structure plays a crucial role in the disease, inhibitor peptides are designed to bind to PrP to prevent abnormal protein folding into an altered conformation that would result in amyloid or amyloid-like deposits or pathological β-sheet precursors thereof, and thus can be used in the treatment of PrP diseases.
- Non-limiting examples of peptides designed to inhibit abnormal folding in the formation of amyloid and amyloid-like deposits, or pathological β-sheet precursors thereof are presented in Table 1. The anti-PrP peptides are designed to bind to the hydrophobic β-sheet forming structural determinant of PrP corresponding to amino acid residues 114 to 125 of prion (presented as SEQ ID NO: 23). While Pro is used as the preferred β-sheet blocking amino acid in virtually all the peptides presented in Table 1, other β-sheet blockers, such as Gly (exemplified in the peptide of SEQ ID NO: 48), Asn and His, are suitable. The peptides of Wood et al., 1995, supra, having the amino acid sequences of SEQ ID NOs: 50-65 are specifically excluded from the peptides of the present invention.
TABLE 1 Examples of Peptides Inhibiting Abnormal Protein Folding 1. Anti-amyloid peptides SEQ ID NO: 7 SEQ ID NO: 8 (iAβ) SEQ ID NO: 9 SEQ ID NO: 10 a) shorter derivatives of iAβ (SEQ ID NO: 8) SEQ ID NO: 15 SEQ ID NO: 16 SEQ ID NO: 17 SEQ ID NO: 18 SEQ ID NO: 19 Pro-Phe-Phe SEQ ID NO: 27 SEQ ID NO: 28 SEQ ID NO: 29 SEQ ID NO: 30 SEQ ID NO: 31 SEQ ID NO: 32 SEQ ID NO: 33 SEQ ID NO: 49 b) derivatives of iAβ with higher hydrophobicity SEQ ID NO: 20 SEQ ID NO: 21 SEQ ID NO: 22 2. Anti-prion (PrP) peptides SEQ ID NO: 24 SEQ ID NO: 25 SEQ ID NO: 38 SEQ ID NO: 39 SEQ ID NO: 40 SEQ ID NO: 41 SEQ ID NO: 42 SEQ ID NO: 43 SEQ ID NO: 44 SEQ ID NO: 45 SEQ ID NO: 46 SEQ ID NO: 47 - Methods for predicting protein conformation to aid in the design of peptide that have a hydrophobic portion and a low probability of abnormally folding into an altered conformation such as a β-sheet are described in Chou and Fasman,Ann. Rev. Biochem. 47:251-276, 1978, Garnier et al., J. Mol. Biol. 120:97-120, 1978, and Minor et al. Nature 371:264-267, 1994.
- A specific non-limiting example of the general preferred design approach described above for designing Aβ inhibitory peptides according to the present invention first identifies the hydrophobic β-sheet forming cluster of Aβ, Leu Val Phe Phe Ala (corresponding to residues 2-6 of SEQ ID NO: 1). The alanine residue which is poorly hydrophobic, can be replaced with the preferred β-sheet blocker, proline, or can be deleted altogether. The Aβ inhibitory peptide in Table 1 having the sequence of SEQ ID NO: 18 is designed to be homologous to amino acid residues 2-6 of SEQ ID NO: 1 where a proline β-sheet blocking residue is substituted for the valine residue, and a charged aspartic acid residue is placed at the end of the peptide. This peptide has a β-sheet blocker interrupting the hydrophobic β-sheet forming cluster of Aβ such that there are no more than three contiguous amino acids corresponding to the hydrophobic β-sheet forming cluster in the hydrophobic portion of the Aβ inhibitory peptide. Not only does the Aβ inhibitory peptide of SEQ ID NO: 18 have a low β-sheet forming potential, but it also substantially retains the hydrophobicity of the hydrophobic β-sheet forming cluster corresponding to residues 2-6 of SEQ ID NO: 1. The charged aspartic acid residue at the end improves the solubility of the peptide. Instead of replacing the valine residue, proline can be designed to replace one of the phenylalanine residues to yield Aβ inhibitory peptides having the sequences of SEQ ID NOs: 27 and 28. Another possibile design to insert a valine into the sequence of SEQ ID NO: 18 to arrive at an inhibitory peptide having the sequence of SEQ ID NO: 17.
- It will be appreciated by those in the art that besides the twenty common naturally occurring amino acids, modified amino acids or naturally occurring but rare amino acids can also be incorporated into the peptides of the present invention. For instance, it was demonstrated that a peptide with amino acid residues in the D-form inhibited fibrillogenesis of Aβ just as well as the peptide with the same sequence of amino acids in the L-form (see Example 1). It will also be appreciated by those of skill in the art that the peptides of the present invention are intended to include pseudo-peptides, semi-peptides, peptoids and peptide mimetics (Kessler,Angew. Chem. Int. Ed. 32:543-544, 1993, Moore, TIPS 15:124-129, 1994) which provide the characteristics of a cluster or portion of at least three hydrophobic residues and one or more β-sheet blockers interrupting this cluster or portion and/or located immediately adjacent to it, so as to have a low probability of forming a β-sheet or β-sheet-like conformation, and thereby inhibiting aggregation/formation of amyloid or amyloid-like deposits or the precursors thereof.
- Modifications to amino acids in the peptides of the invention include, but are not limited to, an amide moiety or a pyroglutamyl residue. These modifications may contribute to decreasing the propensity to form β-sheet conformation or may contribute to peptide stability, solubility, or even immunogenicity. A more stable, soluble and less immunogenic peptide is desirable. Many neuropeptides modified at the C-terminus with a CONH2 (amide) group appear to be resistant to attack by carboxypeptidases and many neuropeptides having a pyroglutamyl residue at the N-terminus are more resistant to attack by broad specificity amino peptides. Also included as peptides of the present invention are cyclic peptides that are resistant to attack by both carboxypeptidases and aminopeptidases.
- As a method of preventing or treating a disorder or disease associated with amyloid or amyloid-like deposits and pathological β-sheet-rich precursors thereof, the inhibitory peptide of the present invention is administered in an effective amount to a subject in need thereof, where the subject can be human or animal. Likewise, a method of detecting such disorders or diseases also includes administering a sufficient amount of the designed peptide to visualize its binding to fibril deposits or precursors thereof by well-known imaging techniques. To facilitate the transport of the peptides of the present invention across the blood-brain barrier, peptides inhibitory to the formation of amyloid deposits in Alzheimer's disease can be preferably complexed with apolipoprotein J, as described in Zlokovic et al.,Biochem. Biophys. Res. Commun. 205:1431-1437, (1994) and Proc. Natl. Acad. Sci. USA 93:4229-4234 (1996). Apolipoprotein J is believed to be a normal carrier for transport of Aβ into the brain parenchyma. The laboratory of the present inventors has found that the region responsible for interacting with apolipoprotein J in Aβ is the sequence corresponding to residues 17-25 of Aβ (SEQ ID NO: 1). Since this sequence is used as a template for the design of Aβ inhibitor peptides, these inhibitor peptides are expected to also be capable of interacting with apolipoprotein J and be transported across the blood-brain barrier using the receptor for apoJ.
- As used herein, the term “prevention” of a condition, such as Alzheimer's disease or other amyloidosis disorders, in a subject involves administering a peptide according to the present invention prior to the clinical onset of the disease. “Treatment” involves administration of the protective peptide after the clinical onset of the disease. For example, successful administration of the peptide of the present invention, after development of a disorder or disease comprises “treatment” of the disease. The invention is useful in the treatment of humans as well as for veterinary uses in animals.
- The peptides of the present invention may be administered by any means that achieves its intended purpose. For example, administration may be by a number of different parenteral routes including, but not limited to, subcutaneous, intravenous, intradermal, intramuscular, intraperitoneal, intracerebral, intranasal, oral, transdermal, or buccal routes. Parenteral administration can be bolus injection or by gradual perfusion over time.
- A typical regimen for preventing, suppressing, or treating a condition associated with amyloid or amyloid-like deposits, comprises either (1) administration of an effective amount in one or two doses of a high concentration of inhibitory peptides in the range of 0.5 to 10 mg of peptide, more preferably 0.5 to 5 mg of peptide, or (2) administration of an effective amount of the peptide administered in multiple doses of lower concentrations of inhibitor peptides in the range of 10-1000 μg, more preferably 50-500 μg over a period of time up to and including several months to several years.
- It is understood that the dosage administered will be dependent upon the age, sex, health, and weight of the recipient, kind of concurrent treatment, if any, frequency of treatment, and the nature of the effect desired. The total dose required for each treatment may be administered by multiple doses or in a single dose. By “effective amount”, it is meant a concentration of inhibitor peptide(s) which is capable of slowing down or inhibiting the formation of amyloid or amyloid-like deposits, or pathological β-sheet precursors thereof, or of dissolving preformed fibril deposits. Such concentrations can be routinely determined by those of skill in the art. It will also be appreciated by those of skill in the art that the dosage may be dependent on the stability of the administered peptide. A less stable peptide may require administration in multiple doses.
- Preparations for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions, and emulsions, which may contain auxiliary agents or excipients which are known in the art. Pharmaceutical compositions such as tablets and capsules can also be prepared according to routine methods.
- Pharmaceutical compositions comprising the peptides of the invention include all compositions wherein the peptide(s) are contained in an amount effective to achieve its intended purpose. In addition, the pharmaceutical compositions may contain suitable pharmaceutically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically. Suitable pharmaceutically acceptable vehicles are well known in the art and are described for example in Gennaro, Alfonso, Ed.,Remington's Pharmaceutical Sciences, 18th Edition 1990, Mack Publishing Co., Easton, Pa., a standard reference text in this field. Pharmaceutically acceptable vehicles can be routinely selected in accordance with the mode of administration and the solubility and stability of the peptides. For example, formulations for intravenous administration may include sterile aqueous solutions which may also contain buffers, diluents and other suitable additives.
- Suitable formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form, for example, water-soluble salts. In addition, suspension of the active compound as appropriate oily injections suspensions may be administered. Suitable lipophilic solvents or vehicles include fatty oils, for example, sesame oil, or synthetic fatty acid ester,s for example ethyl oleate or triglycerides. Aqueous injection suspensions that may contain substances which increase the viscosity of the suspension include, for example, sodium carboxymethyl cellulose, sorbitol, and/or dextran. optionally, the suspension may also contain stabilizers.
- Disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits or into pathological β-sheet-rich precursors of such deposits to be treated or prevented by administering the pharmaceutical composition of the invention includes, but is not limited to, Alzheimer's disease, FAF, Down's syndrome, other amyloidosis disorders, human prion diseases, such as kuru, Creutzfeldt-Jakob Disease (CJD), Gerstmann-Straussler-Scheinker Syndrome (GSS), prion associated human neurodegenerative diseases as well as animal prion diseases such as scrapie, spongiform encephalopathy, transmissible mink encephalopathy and chronic wasting disease of mule deer and elk.
- Besides preventative and therapeutic treatments, the peptides of the invention may also be administered to detect and diagnose the presence or absence of amyloid or amyloid-like deposits in vivo and precursors thereof. A designed peptide capable of binding to a hydrophobic β-sheet forming cluster as a structural determinant in a corresponding amyloid or amyloid-like deposit and precursors thereof, labeled non-radioactively or with a radioisotope, as is well-known in the art, can be administered to a subject for diagnosing the onset or presence of a disease or disorder associated with abnormal protein folding into amyloid or amyloid-like fibril deposits and pathological β-sheet-rich precursors thereof. The binding of such a labeled peptide after administration to amyloid or amyloid-like deposits or precursors thereof can be detected by in vivo imaging techniques known in the art.
- Having now generally described the invention, the same will be more readily understood through reference to the following example which is provided by way of illustration and is not intended to be limiting of the present invention.
- Amyloid deposition appears to be an important factor in the development of neuritic plaque and neuronal disfunction in AD. The results of the study presented below indicate that a short peptide partially homologous to the central hydrophobic region of Aβ (residues 17-21), but containing amino acids which block the adoption of a β-sheet structure binds Aβ, inhibits amyloid formation in vitro and dissolves preformed Aβ fibrils. Furthermore, the inhibitor is able to block the in vivo deposition of AA in the spleen of mice. Since the inhibition of fibrillogenesis and the disassembly of preformed fibrils occurs in the presence of a molar excess of an 11 amino acid peptide, called inhibitor of Aβ fibrillogenesis peptide (iAβ) and also designated as
anti-amyloid peptide 2, the Aβ-Aβ interaction probably has a greater affinity than the Aβ-iAβ interaction. Although a molar excess of iAβ is required to produce the inhibition of amyloid formation, the very low concentration of sAβ present in human body fluids (1-10 nM) would necessitate only 40-400 nM of iAβ for a 40-fold molar excess. - The results of the study support the concept that the formation of a β-sheet secondary structure is important for fibrillogenesis and it is believed that iAβ inhibits amyloid formation by binding to monomeric Aβ peptides thereby blocking the formation of the oligomeric β-sheet conformation precursor of the fibrils. The dissolution of preformed fibrils induced by iAβ may indicate that the monomeric peptide is in equilibrium with the fibrils, as previously suggested (Maggio, J. et al.,Proc. Natl. Acad. Sci. USA 89:5461-5466, 1992; Tamaokoa, A. et al., Biochem. Biophys. Res. Commun. 205:834-842, 1994). The inhibitor may bind to monomeric peptide, thus displacing the equilibrium, and leading to fibril disaggregation.
- Peptide synthesis. Synthetic peptides containing the sequence 1-40, 1-42 of Aβ and the anti-amyloid peptides were synthesized by a solid phase technique on a p-methyl-benzhydrylamine resin using a
Biosearch SAM 2 synthesizer. Peptides were subjected to purification by high performance liquid chromatography (HPLC) with the use of a reverse-phase support medium (Delta-Bondapak) on a 0.78×30 cm column with a 0-80% linear gradient of acetonitrile in 0.1% (v/v) trifluoroacetic acid. The peptide content of the eluate was monitored by measurement of its absorption at 220 nm. Peptide sequences were determined by automatic Edman degradation on a 477A protein sequencer and the PTH derivatives analyzed with an on-line 120 A PTH analyzer (Applied Biosystems, Foster City, Calif.). Purity of the peptides was evaluated by peptide sequencing and laser desorption mass spectrometry. Stock solutions of the peptides were prepared by dissolving them in 50% acetonitrile. The concentration was determined by amino acid composition analysis on a Waters Pico-Tag amino acid analyzer (Millipore Corp, Bedford, Mass.), after hydrolyzing the samples under reduced pressure in the presence of 6M HCl for 20 hours at 110° C. For experiments, peptide aliquots were lyophilized and resuspended in the buffer used in the assay. - Prediction of Secondary Structure. The α-helix, β-sheet and β-turn propensities for different sequences were calculated by the Chou and Fasman secondary structure prediction algorithm (Chou and Fasman,Ann. Rev. Biochem. 47: 251-2760, 1978) using the program Protylze version 3.01 from Copyright.
- Fluorimetric determination of amyloid formation. Aliquots of peptides were incubated for varying amounts of time at room temperature in O.1M Tris-HCl, pH 7.4. To quantitate amyloid formation, a thioflavine T (Tht) fluorescence method was used. Tht binds specifically to amyloid and this binding procedure produces a shift in its emission spectrum and a fluorescent signal proportional to the amount of amyloid formed (Naiki et al., Lab. Invest. 65:104-110, 1991). Thus, this method is very specific for the semiquantitation of amyloid-like aggregates. After incubation Aβ peptides were added to 50 mM glycine, pH 9.2, 2 μM Tht in a final volume of 2 ml. Fluorescence was measured at an excitation wavelength of 435 nm and an emission wavelength of 485 nm using a Hitachi F-2000 fluorescence spectrometer (Hitachi Instruments Inc., San Jose, Calif.). A time scan of fluorescence was performed and three values after the decay reached the plateau (280, 290 and 300 seconds) were averaged after subtracting the background fluorescence of 2 μM Tht.
- Electron microscopy. For fibril formation, peptides (1 mg/ml) were incubated in 0.1 M Tris-HCl, pH 7.4, for 6 days at room temperature. Samples to be visualized were placed on carbon formvar-coated 300-mesh nickel grids for 1 minute, blotted and stained for 1 minute with 2% uranyl acetate under a vapor of 2% glutaraldehyde and visualized on a
Zeiss EM 10 electron microscope (Carl Zeiss, Inc., Thornwood, N.Y.) at 80 kv. - Circular dichroism studies. The secondary structure of Aβ and inhibitor peptides was analyzed by circular dichroism in aqueous solution. Spectra were recorded in a Jasco spectropolarimeter Model J-720 (Jasco Inc., Easton, Md.). Aliquots of peptides at a concentration of 0.1-0.2 mg/ml in 20 mM Tris-HCl, pH 7.4, were first centrifuged to produce a clear solution and the spectra were recorded at 1 nm intervals over the
wavelength range 190 to 260 nm in a 0.1 cm pathlength cell. Results are expressed in terms of mean residue ellipticity in units of deg cm2dmol−1. - Binding sites. The interaction between Aβ an iAβP was studied by fluorescence spectroscopy at 25° C. using a Perkin Elmer model LS50B spectrofluorimeter. 45 μg of Aβ1-40 was dissolved in 300 μl of 5 mM Tris, pH 7.4 and immediately the fluorescence spectra was recorded between 290 nm an 400 nm at excitation 280 nm, with slits set at 2.5 nm bandwidth. Different amounts of lyophilized iAβ were added to the Aβ solution and after 15 min of incubation the fluorescence spectra was recorded, iAβ at the same concentrations did not give any fluorescence signal above the background. The binding of iAβ to Aβ was evaluated by the change in fluorescence intensity at 309nm between the spectra of Aβ alone and in the presence of different concentrations of the inhibitor. The binding data were analyzed with the aid of a curve fitting software (GraphPad Prism version 1.0).
- In vivo studies using the experimental murine model of amyloidosis. Induction of experimental amyloidosis was done as previously described (Merlini et al.,Proc. Natl. Acad. Sci. USA 92:2959-2964, 1995; Snow et al., J. Histochem. Cytochem. 39:1321-1330, 1991). BALB/c mice were injected t.v. with 100 μg of amyloid enhancing factor (AEF) alone or preincubated for 24 h with 5 mg of iAβ. AEF was prepared using the standard protocols. The AEF injection was followed by a single s.c. injection of 0.5 ml of 2% silver nitrate. Animals were sacrificed 5 days after the injection and the amyloid quantitated by immunohistochemistry and congo red staining. A standard set of amyloid containing tissue was generated (5%, 10%, 20%, 30%, 40%, 50%). These were reference points to determine the amount of amyloid in a given tissue. Standard sections were examined under the microscope (Nikon, using polarizing filters to generate birefringence for Congo red). The images were digitized and transferred to a MacIntosh computer for analysis. The digitized images were analyzed for color (intensity and area) under low power (20×) using a Kontron or Prism Image Analysis. Experimental spleen tissue sections were fixed in 10%. buffered formalin and embedded in paraffin and stained with antibodies against SAA. The experimental sections were analyzed and compared to the standards for quantitation of the area spleen containing amyloid. The experiments were performed using four animals per condition.
- Design of inhibitor peptides. The laboratory of the present inventors focused on the central hydrophobic region within the N-terminal domain of Aβ, amino acids 17-21 (corresponding to amino acid residues 2-6 of SEQ ID NO: 1), as a model for the inhibitor peptide (FIGS. 2A and 9). Proline residues were introduced in the inhibitor peptide in order to block β-sheet structure and charged residues were added at the ends of the peptide to increase solubility. Proline was chosen to block β-sheet structure since it rarely forms part of this conformation (Chou et al.,Ann. Rev. Biochem. 47:251-276, 1978) and does not occur in the interior of antiparallel β-sheets (Wouters et al., Protein Sci. 3:43S, 1994), due to the extraordinary characteristics of this amino acid, namely: (a) the nitrogen of the peptide bond is not available to the β-sheet bonding network; (b) the torsion angles of the peptidyl-propyl bond imposed by the proline ring are incompatible with peptide bond geometries found in β-sheet motifs; and (c) the proline ring can not fit sterically within the β-sheet bonding network. Moreover, recent data showed that the introduction of proline residues into short peptides homologous to Aβ resulted in non-amyloidogenic analogues (Wood et al., Biochem. 34:724-730, 1995).
- Based on these criteria, an 11 amino acid peptide, called inhibitor of Aβ fibrillogenesis peptide (iAβ) was designed, which has a low probability of adopting a β-sheet conformation due to the presence of proline residues (FIG. 9). Other peptide inhibitors based on the above criteria are shown in FIG. 2A. The circular dichroism spectrum of iAβ in aqueous solution was typical of unordered structures (FIG. 10). Samples of iAβ at different concentrations as well as samples incubated for several days have similar spectra (FIG. 10). Indeed, iAβ did not aggregate even at high concentrations (4 mg/ml) or after long periods of incubation (more than 30 days).
- The interaction between Aβ and iAβ was studied by monitoring the quenching of Tyr10 fluorescence of Aβ (FIG. 11). Fluorescence spectroscopy was chosen to study the interaction of Aβ-iAβ because this technique has been used extensively for ligand-binding studies and does not require peptide labelling with reagents that may alter their properties. Aβ excited at 280 nm showed a fluorescence spectrum with a maximum at 309 nm (FIG. 11, inset), which is typical of tyrosine emission. The presence of iAβ induced a saturable quenching of the fluorescence, reaching a maximum of 12.6% of the total fluorescence at approximately 4 μM of iAβ (FIG. 11). Non-linear regression analysis of the binding data to a rectangular hyperbola allowed calculation of a relative dissociation constant of 75.9±6.5 nM.
- Inhibition of Aβ amyloid formation and dissolution of preformed fibrils in vitro. The quantitative evaluation of the effect of iAβ on in vitro Aβ fibrillogenesis was based on a fluorometric assay that measures thioflavine T (Tht) fluorescence emission (Soto et al., 1995, supra) . The binding of Tht to amyloid is specific and produces a shift in the emission spectrum of Tht and a fluorescent enhancement proportional to the amount of amyloid (LeVine et al., 1993, supra). FIG. 12 shows the influence of different concentrations of iAβ on fibrillogenesis of the two major variants of Aβ (Aβ1-40 and Aβ1-42). iAβ inhibited in a dose-dependent manner in vitro amyloid formation by both Aβ variants. After 24 h of incubation in the presence of a 5-fold or 20-fold molar excess of iAβ, Aβ1-40 formed only 33.9% and 13.7%, respectively, of the amyloid detectable in the absence of inhibitor (FIG. 12). Although the inhibitor is less efficient with Aβ1-42, a 5-, 20-, and 40-fold molar excess of iAβ over Aβ1-42 resulted in a 28.7%, 72.3% and 80.6% of inhibition, respectively (FIG. 12). Several non-related peptides had no effect on fibrillogenesis or slightly increased Aβ amyloid formation, probably by incorporation into the fibrils. The 12 residue control peptide (SEQ ID NO: 26), did not alter amyloid formation by Aβ1-40 or Aβ1-42 (FIGS. 12 and 13). iAβ inhibited Aβ amyloid formation even after extensive incubation (FIG. 13) and appeared to be a more efficient blocker of fibrillogenesis after several days of incubation.
- The 15-amino acid peptide, designated anti-amyloid peptide 1 (SEQ ID NO: 7) was found to adopt a random coil conformation (FIG. 2B) and was also found to be 90% inhibitory to amyloid fibril formation at 50-fold molar excess over soluble amyloid monomers (FIGS. 5A and 5B).
- In order to evaluate the ability of iAβ to disassemble preformed Aβ fibrils, Aβ1-40 or Aβ1-42 (1 mg/ml) were preincubated for 5 days at 37° C. before the addition of inhibitor peptide. FIG. 14A shows the dissolution of Aβ1-40 or Aβ1-42 fibrils after 24 h incubation with different iAβ concentrations. The inhibitor efficiently affected disaggregation of Aβ1-40 fibrils, achieving almost complete dissolution when used in a 40-fold molar excess. Conversely, only 51% of Aβ1-42 fibril reduction was obtained with the same molar excess of iAβ (FIG. 14). The maximum level of fibril dissolution was obtained after 2 days of incubation with iAβ and remained unaltered thereafter (FIG. 14B).
- The D-form of iAβ to inhibit Aβ fibrillogenesis was compared to the L-form of iAβ and the results shown in FIG. 17 demonstrate that D-iAβ inhibits Aβ fibrillogenesis similarly to L-iAβ. Aβ1-42 (1 mg/ml) was incubated for 24 h in the presence of different molar ratios of the L- and D-form of iAβ. Amyloid was quantitated by the fluorometric assay based on the thioflavine T fluorescence emission and expressed as a percentage of the amyloid obtained in the Aβ sample non-incubated with the inhibitor.
- The inhibition of fibril formation and the dissolution of preformed fibrils by iAβ was also analyzed by negative-staining electron microscopy (FIGS. 15a-f). Aβ1-40 (2 mg/ml) preincubated for 6 days at 37° C. formed typical 8-10 nm unbranched fibrils (Castano et al., biochem. Biophys. Res. Commun. 141:782-789, 1986) (FIG. 15a). When Aβ was incubated from the start with a 40-fold excess of iAβ, only amorphous aggregates were obtained (FIG. 15b). The control peptide under the same conditions did not produce any effect on Aβ fibrillogenesis (FIG. 15e). Fibrils preformed by incubation of Aβ1-40 for 6 days at 37° C. were almost completely dissolved after 2 days of incubation with a 1:40 molar ratio of Aβ:iAβ (FIG. 15c). iAβ or the control peptide incubated under the same conditions used in the experiments shown in FIGS. 15b and 15 e, formed no amyloid-like material (FIGS. 15d and 15 f).
- Dissolution of preformed fibrils also occurred with the 15 amino acid anti-amyloid peptide 1 (FIGS. 6A and 6B). This anti-amyloid peptide also inhibits the fibril formation of other amyloidgenic peptides derived from various other amyloid material, e.g., amyloid-A and the gelsolin related amyloid (FIG. 8).
- Inhibition of in vivo fibrillogenesis using an animal model of amyloidosis related to amyloid-A. A well-characterized mouse model for systemic amyloid-A (AA) deposition was used. This model has been used to test the role of amyloid-associated components such as proteoglycans and apolipoprotein E (Kindy et al.,Lab. Invest. 73:469-476, 1995; Snow et al., 1991, supra) and to test inhibitors of amyloid deposition in vivo (Kisilevsky et al., Nature Med. 1:143-148, 1995; Merlini et al., 1995, supra). Secondary or reactive amyloidosis is an inflammation-associated disorder in which AA protein is deposited in several organs. The AA protein is a 76 residues N-terminal fragment derived from proteolysis of a precursor called serum amyloid A (SAA) protein (Levin et al., 1972, supra).
- Experimental amyloidosis in mice was induced by injection of amyloid enhancing factor (AEF) and silver nitrate. Under these conditions the animals developed amyloid deposits in the spleen after 36-48 h of the injection (Kisilevsky et al., 1983, supra). We examined the effect of iAβ on AA amyloid formation after 5 days. When 5 mg of iAβ were injected together with AEF, after 24 h of preincubation, the area occupied by amyloid in the spleen was decreased in approximately 86.4% in comparison with the animals treated without the inhibitor (Table 2).
TABLE 2 Effect of iAβ on in vivo amyloid deposition using the animal model of amyloid-A amyloidosis. Amyloid was induced by injection of amyloid enhancing factor (AEF) and silver nitrate (SN). Animals were sacrificed at 5 days and amyloid detected immunohistochemically using an antibody to serum amyloid A protein and quantitated by image analysis, as described in Methods. Controla AEF/SN + Animal AEF/SN untreated iAβ b 1 29.4 0.05 4.35 2 31.65 0.1 3.68 3 32.97 0.21 5.32 4 30.77 0.04 3.67 Average ± SEc 31.2 ± 0.75 0.10 ± 0.04 4.26 ± 0.39 - Effect of iAβ on the promotion of Aβ fibrillogenesis induced by apoliprotein E. It is thought that sAβ in human body fluids is complexed to apolipoproteins, especially apolipoprotein (apo) J and E (Frangione et al.,Neurobiol. Aging 15:97-99, 1994). These proteins as well as others (proteoglycans, amyloid P component, α1-antichymotrypsin, etc) are found in senile plaques and congophilic vessels (Coria et al., Lab. Invest. 58:454-457, 1988; Abraham et al., Cell 52:487-501, 1988; Wisniewski et al., Am. J. Pathol. 145:1030-1035, 1994; Snow et al., Neuron. 12:219-234, 1994). Several of these amyloid-associated proteins bind to Aβ in solution and modulate the rate of amyloid formation in vitro (Moore. G. J. Trends Pharmacol. Sci. 15:124-129, 1994; Wisniewski et al., Am. J. Pathol. 145:1030-1035, 1994; Ma et al., Nature 372:92-94, 1994; Snow et al., Neuron. 12:219-234, 1994).
- The results shown in FIG. 18 show that iAβ blocked the promotion of Aβ fibrillogenesis induced by apo E. Preliminary experiments also indicate that heparan-sulfate proteoglycan-induced Aβ fibrillogenesis is blocked as well by iAβ.
- Dissolution of Alzheimer's amyloid plaque by iAβ. Amyloid was isolated from mature senile plaque extracted from a brain of a patient who died of Alzheimer's disease. Grey matter was separated from meninges and white matter, cleaned, chopped and homogenized in buffer containing 0.25M sucrose. The homogenate was subjected to a series of centrifugation, treatment with DNase I and collagenase and to a discontinuous sucrose density gradient. After this procedure, pure amyloid cores containing >90% Aβ and also several of the amyloid-associated proteins was obtained. 10 μg of amyloid proteins was incubated for 5 days without and with 200 μg of iAβ. The amount of amyloid was quantitated by using the fluorometric assay based in the binding of thioflavine T to amyloid, as described (Soto, C., et al.,J. Biol. Chem. 270: 3063-3067, 1995). The material obtained from two different extractions was tested (
Samples 1 and 2) and the average and standard error of three different experiments was shown. - Effect of iAβ on Aβ-induced cell toxicity. Neuronal differentiated human neuroblastoma cells (IMR-32) were obtained from American Type Culture Collection and were grown using the standard protocols. Fresh Aβ1-42 was added to the medium to reach a final concentration of 30 μM. The inhibitor (final concentration 600 μM) was added together or preincubated with Aβ1-42 for 24 h. After 48 h cell toxicity was evaluated by using the lactate dehydrogenase (LDH) release assay (Simmons, et al.,Mol. Pharmacol. 45: 373-379, 1994), using a kit obtained from Sigma. The results shown correspond to the average between two different experiments.
- Shorter iAβ derivatives. Shorter anti-β-sheet peptides were designed using peptide iAβ (SEQ ID NO: 8) as a model (Table 3). Two frequent problems associated with peptides used as drugs in medicine, i.e., transport across the blood-brain barrier and generation of an immunoreactive response, can be minimized by shortening the length of the peptide. Studies on the inhibition of Aβ amyloid formation in vitro by iAβ derivatives showed that a seven (iAβ2) and a five (iAβ4) amino acid residue peptides are similar or better inhibitors than iAβ under the same experimental conditions (Table 3). In Table 3, 30 μg of Aβ peptides were incubated with a 10-fold molar excess of different peptides for 2 days at room temperature in 30 μl of 0.1M tris pH 7.6. The percentage of amyloid remaining after the incubation period was determined by the ThT fluorometric assay. Several control peptides (CP) and short Aβ fragments did not have any significatn efect on Aβ fibrillogenesis.
TABLE 3 Effect of iAβ derivatives on Aβ1-40 and Aβ1-42 amyloid formation Aβ incubated % of amyloid % of amyloid with Sequence Aβ1-42 Aβ1-40 alone 100 ± 1.7 100 ± 1.4 iAβ SEQ ID NO: 8 57.9 ± 1.3 25.5 ± 0.7 iAβ1 SEQ ID NO: 15 85.7 ± 11.6 55.2 ± 2.1 iAβ2 SEQ ID NO: 16 61.3 ± 3.0 36.7 ± 4.8 iAβ3 SEQ ID NO: 17 87.1 ± 6.1 90.1 ± 1.3 iAβ4 SEQ ID NO: 18 45.4 ± 0.6 28.7 ± 1.7 iAβ5 SEQ ID NO: 19 82.4 ± 5.0 92.1 ± 1.3 iAβ6 Pro-Phe-Phe 88.9 ± 2.6 108.1 ± 7.9 CP1 SEQ ID NO: 49 101.3 ± 1.9 98.4 ± 1.2 CP2 SEQ ID NO: 66 125.3 ± 3.9 111.3 ± 4.1 CP3 SEQ ID NO: 67 94.4 ± 1.4 87.7 ± 2.0 Aβ10-20 SEQ ID NO: 68 80.9 ± 1.6 73.1 ± 0.9 Aβ17-21 a.a. 2-6 of 92.3 ± 3.4 89.2 ± 2.7 SEQ ID NO: 1 Aβ18-21 a.a. 3-6 of 98.5 ± 5.3 105 ± 3.2 SEQ ID NO: 1 - Cerebral deposition of PrP amyloid occurs in most of the cases of the PrP-related disorder known as Gerstmann-Straussler-Scheinker (GSS) disease. The major component of amyloid fibrils in GSS brains is a 11-kDa fragment of PrP that spans residues 58 to 150 (Tagliavini, F., et al.EMBO J. 10:513-519, 1991). By using the synthetic peptides homologous to the consecutive segments of GSS-amyloid protein, it has been shown that the PrP fragment 109-141 is critical in conferring the pathological properties of PrPsc (Nguyen, J., et al. Biochem. 34:4186-4192, 1995; Zhang, H., et al., J. Mol. Biol. 250:514-526, 1995; Tagliavini, F. et al. Proc. Natl. Acad. Sci. (USA) 90:9678-9682, 1993). The peptide 109-141 (SEQ ID NO: 37) as well as the peptide fragments 109-122 (SEQ ID NO: 34) and 106-126 (SEQ ID NO: 35), but not peptide fragment 129-141 (SEQ ID NO: 36), formed typical amyloid fibrils (Zhang H. et al. J. Mol. Biol. 250:514-526, 1995; Gassett, Baldwin, Lloyd, et al. 1992; Tagliavini, F., et al. Proc. Natl. Acad. Sci. (USA) 90:9678-9862, 1993). In addition, the PrP fragment 109-122, (which adopts a β-sheet conformation) can convert the unstructured fragment 129-141 into a β-pleated sheet (Nguyen, J., et al. Biochem. 34:4186-4192, 1995). Moreover, the fragments 90-145 and 109-141 are resistant to degradation by proteinase K when they adopt a β-sheet conformation (Zhang, H., et al. J. Mol. Biol. 250:514-526, 1995). Finally, the peptide fragment 90-145, which adopts a β-sheet conformation, can induce the conversion of PrPc into PrPsc in vitro (Kaneko, K. et al., Proc. Natl. Acad. Sci. USA 92:11160-11165, 1995).
- The experiments described below were carried out using a synthetic peptide corresponding to the 109-141 fragment of PrP as a model system for the conformational transition that is observed in the formation of the pathogenic PrPsc isoform. This synthetic peptide corresponding to the sequence 109-141 of PrP, designated PrP 109-141, undergoes spontaneous conversion from an initial random coil to adopt a β-sheet secondary structure in a period of a few days, as evaluated by circular dichroism (FIG. 21), using the conditions described in Nguyen, J. et al. Biochem. 34:4186-4192 (1995). Briefly, aliquots of 80 μg of PrP109-141 were incubated for 0, 1, 3, 5, 7 and 10 days at 37° C. in 350 μl of 0.1M sodium phosphate,
pH - In addition, when the PrP109-141 peptide adopts a β-sheet conformation, it is highly resistant to degradation by proteinase K (FIG. 22), whereas the same peptide in a random coil structure is highly degradable by this protease. This is shown in FIG. 22 where aliquots of PrP109-141 were incubated as indicated above for the circular dichroism study for 7 days to obtain a peptide adopting a β-sheet conformation. The sample was then lyophilized and resuspended in Phosphate buffered saline (PBS). A similar aliquot of the fragment, without pre-incubation (adopting a random coil conformation), was also resuspended in PBS. Both samples were treated with proteinase K (1:400 w/w) for 0, 10, 30 and 60 min. The reaction was stopped by adding 5 mM phenylmethyl-sulphonylfluoride (PMSF) and sample buffer for electrophoresis. Samples having the equivalent of 5 μg of PrP109-141 per lane were separated by SDS electrophoresis in Tris-Tricine buffer (Schagger, H. & vonjagow, G.,Anal. Biochem. 166:368-379, 1987) and stained with Coomasie blue. The result that PrP109-141 in the β-sheet conformation is resistant to proteinase K degradation is very similar to the differences in proteinase K sensitivity observed between PrPsc and PrPc.
- Moreover, the PrP109-141 fragment as well as the PrP fragment 106-126 form typical amyloid fibrils when incubated for several days under physiological conditions, as evaluated by electron microscopy (FIG. 23A). FIGS. 23A and 23B show the electron microscopy pattern obtained when PrP109-141 was incubated alone (FIG. 23A) or in the presence of 10-fold molar excess of iPrP-12aa (FIG. 23B), a prototype PrP peptide inhibitor (12 amino acid residues; SEQ ID NO: 24) that was first screened for its ability to inhibit amyloid formation by PrP fragments in vitro. Aliquots of PrP109-141 (2 mg/ml) were incubated for 7 days at 37° C. without (FIG. 23A) or with (FIG. 23B) 10-fold molar excess of iPrP-12aa. The samples were first centrifuged at 14,000 rpm for 5 min and the pellet was resuspended in half of the initial volume and placed on carbon formar-coated 300-mesh nickel grids. The grids were stained for 60 seconds with 2% uranyl acetate under a vapor of 2% glutaraldehyde and visualized on a
Zeiss EM 10 electron microscope at 80 kV. A reduction in the number of fibrils was clearly observed when the PrP fragment was incubated with the inhibitor. - FIG. 24 shows the dose-dependent inhibition of PrP106-126 fibrillogenesis by iPrP-12aa. Amyloid formation was quantitated by the fluorometric assay, based on the specific interaction of Thioflavine T (Tht) with amyloid fibrils. PrP106-126 at 1 g/μl in PBS, pH 7.4, was incubated for 5 days at 37° C., and at the end of the incubation period, 50 mM glycine, pH 9.2, 2 μM Tht was added in a final volume of 2 ml. Fluorescence was measured at an excitation wavelength of 435 nm and an emission wavelength of 485 nm in a Perkin Elmer, model LS50B fluorescence spectrometer. Approximately, 50% inhibition of amyloid formation was observed in the presence of a 10-fold molar excess of iPrP-12aa. No significant effect was seen when the PrP fragment was incubated with the same concentration of an unrelated peptide of 12 amino acids (CPI; SEQ ID NO: 49). Peptide iPrP-12aa was also able to partially block the conversion of PrP109-141 from a protease-sensitive (random coil conformation) to a protease-resistant form (β-sheet conformation) (FIG. 25). In fact, while almost 100% of the PrP peptide molecules after incubation for 5 days in the absence of the inhibitor were resistant to proteinase K, less than 50% of the PrP peptide molecules were resistant when the PrP fragment was incubated in the presence of a 10-fold molar excess of iPrP-12aa (FIG. 25). Since the differences in protease degradability are associated with the secondary structure adopted by the peptide (FIG. 22), the latter result demonstrates that peptide iPrP-12aa is able to function as a peptide inhibitor and block the conversion of random coil→β-sheet in the peptide model of PrP. This conclusion is supported by direct evaluation of the effect of iPrP-12aa on the conformational transition of PrP109-141 (FIG. 26). When 80 μg aliquots of the 109-141 fragment were incubated alone for 7 days as described previously in this example for circular dichroism studies, the spontaneous transformation of an initial random coil structure to a β-sheet rich conformation was observed. However, when PrP109-141 was incubated under the same conditions, but in the presence of 10 μg of iPrP-12aa (molar ratio peptide inhibitor=2.5:1), the extent of conformational change was clearly lower (FIG. 26). In short, these results indicate that anti-β sheet peptides designed to interact with PrP109-141 in view of the PrP sequence can be used to prevent the in vitro transformation of PrPc→PrPsc, as determined by using the peptide model system described above.
- Having now fully described this invention, it will be appreciated by those skilled in the art that the same can be performed within a wide range of equivalent parameters, concentrations, and conditions without departing from the spirit and scope of the invention and without undue experimentation.
- While this invention has been described in connection with specific embodiments thereof, it will be understood that it is capable of further modifications. This application is intended to cover any variations, uses, or adaptations of the inventions following, in general, the principles of the invention and including such departures from the present disclosure as come within known or customary practice within the art to which the invention pertains and as may be applied to the essential features hereinbefore set forth as follows in the scope of the appended claims.
- All references cited herein, including journal articles or abstracts, published or corresponding U.S. or foreign patent applications, issued U.S. or foreign patents, or any other references, are entirely incorporated by reference herein, including all data, tables, figures, and text presented in the cited references. Additionally, the entire contents of the references cited within the references cited herein are also entirely incorporated by reference.
- Reference to known method steps, conventional methods steps, known methods or conventional methods is not in any way an admission that any aspect, description or embodiment of the present invention is disclosed, taught or suggested in the relevant art.
- The foregoing description of the specific embodiments will so fully reveal the general nature of the invention that others can, by applying knowledge within the skill of the art (including the contents of the references cited herein), readily modify and/or adapt for various applications such specific embodiments, without undue experimentation, without departing from the general concept of the present invention. Therefore, such adaptations and modifications are intended to be within the meaning and range of equivalents of the disclosed embodiments, based on the teaching and guidance presented herein. It is to be understood that the phraseology or terminology herein is for the purpose of description and not of limitation, such that the terminology or phraseology of the present specification is to be interpreted by the skilled artisan in light of the teachings and guidance presented herein, in combination with the knowledge of one of ordinary skill in the art.
-
0 SEQUENCE LISTING (1) GENERAL INFORMATION: (iii) NUMBER OF SEQUENCES: 69 (2) INFORMATION FOR SEQ ID NO: 1: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 1: Lys Leu Val Phe Phe Ala Glu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 2: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 2: Arg Ser Phe Phe Ser Phe Leu Gly 1 5 (2) INFORMATION FOR SEQ ID NO: 3: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 3: Asp Cys Phe Ile Leu Asp Leu Gly 1 5 (2) INFORMATION FOR SEQ ID NO: 4: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 4: Arg Val Thr Ile Thr Cys Gln Ala 1 5 (2) INFORMATION FOR SEQ ID NO: 5: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 5: Ser Phe Tyr Leu Leu Tyr Tyr Thr 1 5 (2) INFORMATION FOR SEQ ID NO: 6: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 6: Asp Leu Ala Thr Val Tyr Val Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 7: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 7: Ser Arg Gly Asp Leu Pro Phe Phe Pro Val Pro Ile Gly Asp Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 8: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 8: Arg Asp Leu Pro Phe Phe Pro Val Pro Ile Asp 1 5 10 (2) INFORMATION FOR SEQ ID NO: 9: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 9: Arg Asp Phe Ile Pro Leu Pro Leu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 10: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 10: Arg Asp Tyr Leu Pro Tyr Tyr Pro Leu Asp 1 5 10 (2) INFORMATION FOR SEQ ID NO: 11: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 18 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 11: Gly Lys Met Ser Ser Tyr Ala Phe Phe Val Gln Thr Cys Arg Glu Glu 1 5 10 15 His Lys (2) INFORMATION FOR SEQ ID NO: 12: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 12: Phe Asn Asn Gly Asp Cys Phe Ile Leu Asp Leu Gly Asn Asn Ile 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 13: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 13: Arg Ser Phe Phe Ser Phe Leu Gly Glu Ala Phe Asp Gly Ala Arg 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 14: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 14: Gln Lys Leu Val Phe Phe Ala Glu Asp Val Gly 1 5 10 (2) INFORMATION FOR SEQ ID NO: 15: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 15: Arg Asp Leu Pro Phe Phe Pro Val Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 16: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 7 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 16: Leu Pro Phe Phe Pro Val Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 17: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 17: Leu Pro Phe Phe Val Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 18: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 18: Leu Pro Phe Phe Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 19: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 19: Leu Pro Phe Phe 1 (2) INFORMATION FOR SEQ ID NO: 20: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 20: Arg Asp Leu Pro Ile Val Pro Leu Pro Ile Asp 1 5 10 (2) INFORMATION FOR SEQ ID NO: 21: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 7 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 21: Leu Pro Ile Val Pro Leu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 22: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 22: Leu Pro Ile Val Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 23: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 12 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 23: Gly Ala Ala Ala Ala Gly Ala Val Val Gly Gly Leu 1 5 10 (2) INFORMATION FOR SEQ ID NO: 24: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 12 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 24: Arg Asp Ala Pro Ala Ala Pro Val Val Pro Leu Asp 1 5 10 (2) INFORMATION FOR SEQ ID NO: 25: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 7 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 25: Ala Ala Pro Val Val Pro Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 26: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 12 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 26: Val His Val Ser Glu Glu Gly Thr Glu Pro Glu Ala 1 5 10 (2) INFORMATION FOR SEQ ID NO: 27: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 27: Leu Val Pro Phe Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 28: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 28: Leu Phe Pro Phe Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 29: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 29: Pro Leu Phe Phe Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 30: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 30: Leu Val Phe Pro Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 31: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 31: Lys Leu Pro Phe Phe 1 5 (2) INFORMATION FOR SEQ ID NO: 32: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 32: Lys Leu Val Pro Phe 1 5 (2) INFORMATION FOR SEQ ID NO: 33: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 33: Lys Pro Val Phe Phe 1 5 (2) INFORMATION FOR SEQ ID NO: 34: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 14 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 34: Met Lys His Met Ala Gly Ala Ala Ala Ala Gly Ala Val Val 1 5 10 (2) INFORMATION FOR SEQ ID NO: 35: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 21 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 35: Lys Thr Asn Met Lys His Met Ala Gly Ala Ala Ala Ala Gly Ala Val 1 5 10 15 Val Gly Gly Leu Gly 20 (2) INFORMATION FOR SEQ ID NO: 36: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 36: Met Leu Gly Ser Ala Met Ser Arg Pro Met Met His Phe 1 5 10 (2) INFORMATION FOR SEQ ID NO: 37: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 33 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 37: Met Lys His Met Ala Gly Ala Ala Ala Ala Gly Ala Val Val Gly Gly 1 5 10 15 Leu Gly Gly Tyr Met Leu Gly Ser Ala Met Ser Arg Pro Met Met His 20 25 30 Phe (2) INFORMATION FOR SEQ ID NO: 38: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 38: Arg Asp Ala Pro Ala Ala Pro Ala Gly Pro Val Val Pro Leu Asp 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 39: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 14 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 39: Arg Asp Ala Pro Ala Ala Pro Ala Gly Val Pro Val Leu Asp 1 5 10 (2) INFORMATION FOR SEQ ID NO: 40: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 40: Asp Ala Pro Ala Ala Pro Ala Gly Pro Ala Val Pro Val 1 5 10 (2) INFORMATION FOR SEQ ID NO: 41: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 41: Asp Ala Ala Ala Pro Ala Gly Ala Pro Val Val 1 5 10 (2) INFORMATION FOR SEQ ID NO: 42: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 42: Asp Ala Pro Ala Ala Pro Ala Val Pro Val 1 5 10 (2) INFORMATION FOR SEQ ID NO: 43: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 43: Asp Ala Ala Pro Ala Ala Pro Val Val 1 5 (2) INFORMATION FOR SEQ ID NO: 44: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 8 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 44: Asp Ala Pro Ala Ala Pro Val Val 1 5 (2) INFORMATION FOR SEQ ID NO: 45: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 7 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 45: Asp Ala Ala Pro Val Val Pro 1 5 (2) INFORMATION FOR SEQ ID NO: 46: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 46: Asp Ala Ala Pro Val Val 1 5 (2) INFORMATION FOR SEQ ID NO: 47: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 47: Ala Ala Pro Val Val 1 5 (2) INFORMATION FOR SEQ ID NO: 48: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 48: Arg Asp Leu Gly Phe Phe Pro Val Pro Gly Asp 1 5 10 (2) INFORMATION FOR SEQ ID NO: 49: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 49: Val His Val Ser Glu Glu Gly Thr Glu Pro Ala 1 5 10 (2) INFORMATION FOR SEQ ID NO: 50: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 50: Lys Lys Pro Val Phe Phe Ala Glu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 51: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 51: Lys Lys Leu Pro Phe Phe Ala Glu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 52: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 52: Lys Lys Leu Val Pro Phe Ala Glu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 53: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 53: Lys Lys Leu Val Phe Pro Ala Glu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 54: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 54: Lys Lys Leu Val Phe Phe Pro Glu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 55: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 55: Val His His Gln Lys Leu Val Pro Phe Ala Glu Asp Val Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 56: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 56: Val Pro His Gln Lys Leu Val Phe Phe Ala Glu Asp Val Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 57: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 57: Val His Pro Gln Lys Leu Val Phe Phe Ala Glu Asp Val Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 58: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 58: Val His His Pro Lys Leu Val Phe Phe Ala Glu Asp Val Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 59: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 59: Val His His Gln Pro Leu Val Phe Phe Ala Glu Asp Val Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 60: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 60: Val His His Gln Lys Leu Val Phe Phe Ala Pro Asp Val Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 61: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 61: Val His His Gln Lys Leu Val Phe Phe Ala Glu Pro Val Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 62: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 62: Val His His Gln Lys Val Leu Phe Phe Ala Glu Asp Pro Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 63: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 63: Val His His Gln Lys Leu Val Phe Phe Ala Glu Asp Val Pro Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 64: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 64: Lys Lys Leu Val Phe Phe Ala Glu Asp 1 5 (2) INFORMATION FOR SEQ ID NO: 65: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 65: Val His His Gln Lys Leu Val Phe Phe Ala Glu Asp Val Gly Ser 1 5 10 15 (2) INFORMATION FOR SEQ ID NO: 66: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 66: Gly Tyr Leu Thr Val Ala Ala Val Phe Arg Gly 1 5 10 (2) INFORMATION FOR SEQ ID NO: 67: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 12 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 67: Pro Ala Asp Val Pro Leu Ala Pro Arg Ala Val Asp 1 5 10 (2) INFORMATION FOR SEQ ID NO: 68: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 68: Tyr Glu Val His His Gln Lys Leu Val Phe Phe 1 5 10 (2) INFORMATION FOR SEQ ID NO: 69: (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4 amino acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: peptide (ix) FEATURE: (D) OTHER INFORMATION: ′Xaa′ in position one is a cationic amino acid ′Xaa′ in position two is a cationic amino acid ′Xaa′ in position three is a neutral amino acid ′Xaa′ in position four is a cationic amino acid (ix) FEATURE: (ix) FEATURE: (ix) FEATURE: (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 69: Xaa Xaa Xaa Xaa
Claims (8)
1. An isolated inhibitory peptide, comprising a portion of at least three amino acid residues, which portion is hydrophobic and has one or more β-sheet blocking amino acid residues therein, said inhibitory peptide consisting of a sequence predicted not to adopt a β-sheet structure as calculated by the Chou and Fasman secondary structure prediction algorithm, with the proviso that said inhibitory peptide is not any of the following peptides: SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 53, SEQ ID NO: 54, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO:62, SEQ ID NO: 63, SEQ ID NO: 64, and SEQ ID NO: 65, wherein said inhibitory peptide associates with a hydrophobic β-sheet cluster on a protein or peptide involved in the abnormal folding into a β-sheet structure and in the formation of amyloid or amyloid-like deposits, or pathological β-sheet precursors thereof, to structurally block the abnormal folding of said protein or peptide.
2. The isolated inhibitory peptide in accordance with claim 1 , wherein said hydrophobic portion of said inhibitory peptide comprises at least three residues identical to said hydrophobic β-sheet forming cluster of said protein or peptide, wherein said hydrophobic portion is interrupted by one or more β-sheet blocking amino acid residues to prevent having more than three contiguous amino acids within said hydrophobic portion to be identical to the corresponding amino acids in said hydrophobic β-sheet forming cluster of said protein or peptide, and wherein any non-hydrophobic residues in said cluster are optionally deleted in said inhibitory peptide.
3. The isolated inhibitory peptide in accordance with claim 2 , wherein any non-hydrophobic residues in said cluster are deleted in said inhibitory peptide.
4. The isolated inhibitory peptide in accordance with claim 1 , wherein said one or more β-sheet blocking amino acid residues is selected from the group consisting of Pro, Gly, Asn, and His.
5. The isolated inhibitory peptide in accordance with claim 1 , wherein said one or more β-sheet blocking amino acid residues are Pro.
6. The isolated inhibitory peptide in accordance with claim 1 , wherein one or more charged residues are present on one or both ends of said inhibitory peptide to improve the solubility of said inhibitory peptide.
7. The isolated inhibitory peptide in accordance with claim 1 , wherein at least some amino acid residues of said sequence are D-amino acid residues.
8. A composition, comprising the isolated inhibitory peptide of claim 1 and a pharmaceutically acceptable carrier.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/235,483 US20030087407A1 (en) | 1995-06-07 | 2002-09-06 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47832695A | 1995-06-07 | 1995-06-07 | |
US08/630,645 US5948763A (en) | 1995-06-07 | 1996-04-10 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
US08/766,596 US6462171B1 (en) | 1995-06-07 | 1996-12-12 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
US10/235,483 US20030087407A1 (en) | 1995-06-07 | 2002-09-06 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/766,596 Continuation US6462171B1 (en) | 1995-06-07 | 1996-12-12 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
Publications (1)
Publication Number | Publication Date |
---|---|
US20030087407A1 true US20030087407A1 (en) | 2003-05-08 |
Family
ID=27045861
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/630,645 Expired - Lifetime US5948763A (en) | 1995-06-07 | 1996-04-10 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
US08/766,596 Expired - Lifetime US6462171B1 (en) | 1995-06-07 | 1996-12-12 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
US10/235,483 Abandoned US20030087407A1 (en) | 1995-06-07 | 2002-09-06 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/630,645 Expired - Lifetime US5948763A (en) | 1995-06-07 | 1996-04-10 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
US08/766,596 Expired - Lifetime US6462171B1 (en) | 1995-06-07 | 1996-12-12 | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits |
Country Status (8)
Country | Link |
---|---|
US (3) | US5948763A (en) |
EP (1) | EP0843516B1 (en) |
JP (1) | JP2001519753A (en) |
AT (1) | ATE369379T1 (en) |
AU (1) | AU715662B2 (en) |
CA (1) | CA2222690A1 (en) |
DE (1) | DE69637199T2 (en) |
WO (1) | WO1996039834A1 (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040121960A1 (en) * | 1999-11-05 | 2004-06-24 | Claudio Soto-Jara | Peptide analogs and mimetics suitable for in vivo use in the treatment of diseases associated with abnormal protein folding into amyloid, amyloid like deposits or beta sheet rich pathological precursor thereof |
US20070003552A1 (en) * | 2002-07-09 | 2007-01-04 | Gebbink Martijn F B | Cross-beta structure comprising amyloid binding proteins and methods for detection of the cross-beta structure, for modulating cross-beta structures fibril formation and for modulating cross-beta structure-mediated toxicity and method for interfering with blood coagulation |
US20070015133A1 (en) * | 2005-07-13 | 2007-01-18 | Umc Utrecht Holding B.V. | Method for detecting and/or removing protein and/or peptide comprising a cross-beta structure from an aqueous solution comprising a protein |
US20070015206A1 (en) * | 2005-07-13 | 2007-01-18 | Umc Utrecht Holding B.V. | Method for detecting and/or removing protien comprising a cross-beta structure from a pharmaceutical composition |
US20080118529A1 (en) * | 2005-07-13 | 2008-05-22 | Gebbink Martijn Frans Ben Gera | Adjuvation Through Cross -Beta Structure |
US20080241165A1 (en) * | 2002-07-09 | 2008-10-02 | Crossbeta Biosciences B.V. | Cross-beta structure comprising amyloid-binding proteins and methods for detection of the cross-beta structure, for modulating cross-beta structures fiber formation and modulating cross-beta structure-mediated toxicity |
US20080267948A1 (en) * | 2005-07-13 | 2008-10-30 | Martijn Frans Ben Gerard Gebbink | Croos-B Structure Binding Compounds |
WO2008134034A1 (en) * | 2007-04-26 | 2008-11-06 | Yale University | Prion protein as a receptor for amyloid-beta oligomers |
US20090142377A1 (en) * | 2007-11-08 | 2009-06-04 | Crossbeta Biosciences B.V. | Immunogenic compositions |
US20090155254A1 (en) * | 2006-02-16 | 2009-06-18 | Martijn Frans Ben Gerard Gebbink | Affinity Regions |
US20100099609A1 (en) * | 2008-07-28 | 2010-04-22 | Buck Institute For Age Research | eAPP AND DERIVATIVES FOR TREATMENT OF ALZHEIMER'S DISEASE |
US20110008376A1 (en) * | 2007-11-08 | 2011-01-13 | Martijn Frans Ben Gerard Gebbink | Immunogenic compositions capable of activating t-cells |
US10808034B2 (en) | 2016-04-15 | 2020-10-20 | Medimmune Limited | Anti-PrP antibodies and uses thereof |
Families Citing this family (81)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0866805A1 (en) * | 1995-12-12 | 1998-09-30 | Karolinska Innovations AB | PEPTIDE BINDING THE KLVFF-SEQUENCE OF AMYLOID $g(b) |
WO1998030229A1 (en) * | 1997-01-10 | 1998-07-16 | Massachusetts Institute Of Technology | TREATMENTS FOR NEUROTOXICITY IN ALZHEIMER'S DISEASE BY β-AMYLOID PEPTIDES |
US6942963B1 (en) | 1997-01-10 | 2005-09-13 | Massachusetts Institute Of Technology | Methods for identifying treatments for neurotoxicity in Alzheimer's disease caused by β-amyloid peptides |
WO1998036059A2 (en) * | 1997-02-14 | 1998-08-20 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Prion propagation inhibition by dominant-negative prion protein mutants |
DE19725619A1 (en) * | 1997-06-17 | 1998-12-24 | Fraunhofer Ges Forschung | Peptides as agonists and / or inhibitors of amyloid formation and cytotoxicity as well as for use in Alzheimer's disease, in type II diabetes mellitus and in spongiform encephalopathies |
GB9714276D0 (en) * | 1997-07-08 | 1997-09-10 | Univ Dundee | Peptides and related compounds |
US6472140B1 (en) | 1997-09-05 | 2002-10-29 | The General Hospital Corporation | α-2- macroglobulin therapies and drug screening methods for Alzheimer's disease. |
US6342350B1 (en) | 1997-09-05 | 2002-01-29 | The General Hospital Corporation | Alpha-2-macroglobulin diagnostic test |
US7212924B1 (en) * | 1997-10-02 | 2007-05-01 | Akiko Itai | Method of inferring three-dimensional structure of protein |
US8003612B2 (en) * | 1997-10-08 | 2011-08-23 | Proteotech Inc. | Small peptides for the treatment of Alzheimer's disease and other beta-amyloid protein disorders |
US7964192B1 (en) | 1997-12-02 | 2011-06-21 | Janssen Alzheimer Immunotherapy | Prevention and treatment of amyloidgenic disease |
US20080050367A1 (en) | 1998-04-07 | 2008-02-28 | Guriq Basi | Humanized antibodies that recognize beta amyloid peptide |
TWI239847B (en) | 1997-12-02 | 2005-09-21 | Elan Pharm Inc | N-terminal fragment of Abeta peptide and an adjuvant for preventing and treating amyloidogenic disease |
US7790856B2 (en) | 1998-04-07 | 2010-09-07 | Janssen Alzheimer Immunotherapy | Humanized antibodies that recognize beta amyloid peptide |
US7799535B1 (en) | 1997-12-09 | 2010-09-21 | Arch Development Corporation | Methods for identifying factors that control the folding of amyloid proteins of diverse origin |
US6211149B1 (en) | 1998-08-03 | 2001-04-03 | The United States Of America As Represented By The Department Of Health And Human Services | Inhibitors of formation of protease resistant prion protein |
GB2348203B (en) | 1998-11-04 | 2002-06-19 | Imp College Innovations Ltd | Solube beta-forms of prion proteins, methods of preparation and use |
CN1157224C (en) * | 1999-02-18 | 2004-07-14 | 科研制药株式会社 | Novel amide derivs. as growth hormone secretagogues |
US7060670B1 (en) * | 1999-05-05 | 2006-06-13 | Neurochem (International) Limited | Stereoselective antifibrillogenic peptides and peptidomimetics thereof |
UA81216C2 (en) * | 1999-06-01 | 2007-12-25 | Prevention and treatment of amyloid disease | |
US7041807B1 (en) | 1999-06-23 | 2006-05-09 | Caprion Pharmaceuticals, Inc. | Antibodies to a YYX epitope of a mammalian prion protein |
AU6524500A (en) | 1999-08-04 | 2001-03-05 | Northwestern University | Amyloid beta protein (globular assembly and uses thereof) |
WO2001034631A2 (en) * | 1999-11-05 | 2001-05-17 | Axonyx, Inc. | PEPTIDE ANALOGS AND MIMETICS SUITABLE FOR IN VIVO USE IN THE TREATMENT OF DISEASES ASSOCIATED WITH ABNORMAL PROTEIN FOLDING INTO AMYLOID, AMYLOID-LIKE DEPOSITS OR β-SHEET RICH PATHOLOGICAL PRECURSOR THEREOF |
CN1434706A (en) | 1999-12-23 | 2003-08-06 | 神经化学公司 | Compounds and methods for modulating cerebral anyloid angiopathy |
CN1249085C (en) | 2000-05-22 | 2006-04-05 | 纽约大学 | Synthetic immunogenic but non-amyloidogenic peptides homologous to amyloid beta for induction of immune response to amyloid beta and amyloid deposits |
IL148202A0 (en) * | 2000-06-20 | 2002-09-12 | Caprion Pharmaceuticals Inc | Copolymers and methods of treating prion-related diseases |
WO2002035987A2 (en) * | 2000-11-03 | 2002-05-10 | Massachusetts Institute Of Technology | METHODS FOR IDENTIFYING TREATMENTS FOR NEUROTOXICITY IN ALZHEIMER'S DISEASE CAUSED BY β-AMYLOID PEPTIDES |
US7067550B2 (en) * | 2000-11-03 | 2006-06-27 | Massachusetts Institute Of Technology | Treatments for neurotoxicity in Alzheimer's Disease |
US6716589B2 (en) | 2000-11-20 | 2004-04-06 | Alphabeta Ab | Discordant helix stabilization for prevention of amyloid formation |
US7700751B2 (en) | 2000-12-06 | 2010-04-20 | Janssen Alzheimer Immunotherapy | Humanized antibodies that recognize β-amyloid peptide |
DE10104480A1 (en) * | 2001-01-31 | 2002-08-14 | November Ag Molekulare Medizin | Method, use and kit for finding drugs against diseases associated with specific proteins |
WO2002074931A2 (en) * | 2001-03-20 | 2002-09-26 | University Of Chicago | Inhibitors and disassemblers of fibrillogenesis |
US6613505B2 (en) | 2001-04-12 | 2003-09-02 | Bioresource International, Inc. | Composition and method for destruction of infetious prion proteins |
US7521479B2 (en) * | 2001-04-16 | 2009-04-21 | Panacea Pharmaceuticals, Inc. | Methods of treating prion disease in mammals |
EP1395833B1 (en) * | 2001-05-31 | 2013-02-27 | Adlyfe, Inc. | Misfolded protein sensor method |
US7479482B2 (en) * | 2001-11-21 | 2009-01-20 | New York University | Synthetic immunogenic but non-deposit-forming polypeptides and peptides homologous to amyloid β, prion protein, amylin, α-synuclein, or polyglutamine repeats for induction of an immune response thereto |
AU2002360696A1 (en) * | 2001-12-21 | 2003-07-30 | Ilex Oncology, Inc. | Combination comprising anti-cd52 antibodies and other therapeutic agents for treatment for multiple sclerosis |
WO2005000193A2 (en) * | 2003-06-30 | 2005-01-06 | Tel Aviv University Future Technology Development L.P. | Peptides antibodies directed thereagainst and methods using same for diagnosing and treating amyloid-associated diseases |
US20040052928A1 (en) | 2002-09-06 | 2004-03-18 | Ehud Gazit | Peptides and methods using same for diagnosing and treating amyloid-associated diseases |
AU2004203461B2 (en) * | 2002-01-31 | 2009-09-03 | Tel Aviv University Future Technology Development L.P. | Peptides Antibodies Directed Thereagainst and Methods Using Same for Diagnosing and Treating Amyloid-Associated Diseases |
MY139983A (en) | 2002-03-12 | 2009-11-30 | Janssen Alzheimer Immunotherap | Humanized antibodies that recognize beta amyloid peptide |
GB0209384D0 (en) * | 2002-04-24 | 2002-06-05 | Pepsyn Ltd | Peptide composition |
DE10221052A1 (en) * | 2002-05-10 | 2003-12-04 | Transmit Technologietransfer | Active substances for therapy, diagnostics and prophylaxis of diseases in which abnormal protein structures occur |
WO2003105677A2 (en) * | 2002-06-01 | 2003-12-24 | Praecis Pharmaceuticals, Inc. | Methods for treating viral diseases using modulators of amyloidogenic peptide aggregation |
DE10230141B4 (en) * | 2002-07-04 | 2004-07-15 | Priontype Gmbh | Method and kit for the enrichment and detection of modified prion proteins (PrPSc) |
US20040072236A1 (en) | 2002-09-27 | 2004-04-15 | Neil Cashman | PrPSc -interacting molecules and uses thereof |
AR042258A1 (en) * | 2002-12-02 | 2005-06-15 | Applied Research Systems | AZA PEPTIDES |
ATE529744T1 (en) * | 2002-12-03 | 2011-11-15 | Pathogen Removal & Diagnostic Technologies Inc | PRION PROTEIN LIGANDS AND METHODS OF USE THEREOF |
WO2004056318A2 (en) * | 2002-12-19 | 2004-07-08 | New York University | Method for treating amyloid disease |
US20070155955A1 (en) * | 2003-03-18 | 2007-07-05 | Applied Research Systems Ars Holding N.V. | Amylin aggregation inhibitors and use thereof |
WO2004087733A2 (en) * | 2003-03-28 | 2004-10-14 | New York University | Prevention and treatment of alzheimer amyloid deposition |
US7335644B2 (en) * | 2003-03-31 | 2008-02-26 | Council Of Scientific And Industrial Research | Anti-hypertensive molecules and process for preparation thereof |
JP5133561B2 (en) * | 2003-06-19 | 2013-01-30 | メルク セローノ ソシエテ アノニム | Use of factors that regulate prion conversion |
NZ580256A (en) | 2003-08-13 | 2011-07-29 | Novartis Vaccines & Diagnostic | Prion-specific peptide reagents comprising the sequence KKRPKPGG |
EP1725870A1 (en) * | 2004-03-18 | 2006-11-29 | Applied Research Systems ARS Holding N.V. | Anti-lipid rafts antibodies |
ES2434732T3 (en) | 2004-12-15 | 2013-12-17 | Janssen Alzheimer Immunotherapy | Humanized beta-amyloid antibodies for use in improving cognition |
WO2006076497A2 (en) * | 2005-01-13 | 2006-07-20 | Novartis Vaccines And Diagnostics Inc. | Osplation of pathogenic prions |
WO2006076683A2 (en) * | 2005-01-13 | 2006-07-20 | Novartis Vaccines And Diagnostics Inc. | Isolation and detection of pathogenic prions |
CN101356186A (en) * | 2005-09-09 | 2009-01-28 | 诺华有限公司 | Prion-specific peptidomimetic reagents |
US8784810B2 (en) | 2006-04-18 | 2014-07-22 | Janssen Alzheimer Immunotherapy | Treatment of amyloidogenic diseases |
WO2007126111A1 (en) * | 2006-04-28 | 2007-11-08 | Kagoshima University | PEPTIDE CAPABLE OF INHIBITING AMYLOID-β FIBROSIS |
WO2008022035A2 (en) * | 2006-08-10 | 2008-02-21 | The Scripps Research Institute | Methods for identifying cellular modulators of disaggregation activity or aggregation activity in an animal |
JP2010518064A (en) | 2007-02-12 | 2010-05-27 | メルク・シャープ・エンド・ドーム・コーポレイション | Piperazine derivatives for the treatment of AD and related conditions |
US8003097B2 (en) | 2007-04-18 | 2011-08-23 | Janssen Alzheimer Immunotherapy | Treatment of cerebral amyloid angiopathy |
DK2182983T3 (en) | 2007-07-27 | 2014-07-14 | Janssen Alzheimer Immunotherap | TREATMENT OF AMYLOIDOGENIC DISEASES WITH HUMANIZED ANTI-ABETA ANTIBODIES |
EP2175879A4 (en) * | 2007-08-09 | 2010-09-22 | Sylvan Pharmaceuticals Pty Ltd | Treatment of prion protein related diseases |
JO3076B1 (en) | 2007-10-17 | 2017-03-15 | Janssen Alzheimer Immunotherap | Immunotherapy regimes dependent on apoe status |
CN102083450A (en) * | 2008-04-30 | 2011-06-01 | 诺华有限公司 | Assay for pathogenic conformers |
US9242010B2 (en) | 2008-05-16 | 2016-01-26 | Research Foundation Of The City University Of New York | Living copolymer-protein/peptide hybrids for biomedical applications |
EP2303315A1 (en) * | 2008-05-22 | 2011-04-06 | Ramot at Tel Aviv University Ltd. | Method for treating disease characterized by plaque |
WO2010062570A2 (en) * | 2008-10-27 | 2010-06-03 | Recombinant Technologies Llc | COMPOSITIONS COMPRISING CAPTURE PEPTIDES FOR A β-AMYLOID PEPTIDE |
US9067981B1 (en) | 2008-10-30 | 2015-06-30 | Janssen Sciences Ireland Uc | Hybrid amyloid-beta antibodies |
US8409584B2 (en) | 2009-05-05 | 2013-04-02 | New York University | Immunotherapy targeting of the shared abnormal conformational state of amyloidogenic peptides/proteins |
EP2273273A1 (en) | 2009-07-11 | 2011-01-12 | Rheinische Friedrich-Wilhelms-Universität Bonn | Inhibitors of the nitration of amyloid ß peptides and their uses in the diagnosis and treatment of alzheimer's disease |
JP5911503B2 (en) | 2010-11-15 | 2016-04-27 | ラモット・アット・テル・アビブ・ユニバーシテイ・リミテッドRamot At Tel Aviv University Ltd. | Dipeptide analogs for treating amyloid fibril formation-related conditions |
SG187271A1 (en) * | 2011-07-07 | 2013-02-28 | Agency Science Tech & Res | Anti-amyloidogenic, alpha-helix breaking ultra-small peptide therapeutic |
WO2013012811A2 (en) | 2011-07-19 | 2013-01-24 | New York University | Immunotherapeutic modulation of amyloidogenic disease using non-fibrillogenic, non-amyloidogenic polymerized proteins and peptides |
US8906382B2 (en) | 2011-07-19 | 2014-12-09 | New York University | Method for treating amyloid disease |
AU2012358269B2 (en) | 2011-12-22 | 2017-11-02 | Children's Medical Center Corporation | Saposin-A derived peptides and uses thereof |
CN114057858B (en) | 2020-08-10 | 2023-03-21 | 上海瑞吉康生物医药有限公司 | Polypeptides having a disaggregating effect on protein aggregation causing neurodegenerative and neurodegenerative diseases |
DE202022107272U1 (en) | 2022-12-28 | 2023-01-30 | Centurion University of Technology and Management | A system for analysis of Pseudomonas syringae infection by targeting cochaperones containing a J-domain |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5169933A (en) * | 1988-08-15 | 1992-12-08 | Neorx Corporation | Covalently-linked complexes and methods for enhanced cytotoxicity and imaging |
US5547931A (en) * | 1994-02-23 | 1996-08-20 | Immtech International Inc. | Methods of stimulatory thrombocytopoiesis using modified C-reactive protein |
US5817626A (en) * | 1995-03-14 | 1998-10-06 | Praecis Pharmaceuticals Incorporated | Modulators of beta-amyloid peptide aggregation |
US5854215A (en) * | 1995-03-14 | 1998-12-29 | Praecis Pharmaceuticals Incorporated | Modulators of β-amyloid peptide aggregation |
US5854204A (en) * | 1995-03-14 | 1998-12-29 | Praecis Pharmaceuticals, Inc. | Aβ peptides that modulate β-amyloid aggregation |
US5935778A (en) * | 1995-02-09 | 1999-08-10 | Boehringer Mannheim Gmbh | Method for serological typing using type-specific antigens |
US5985242A (en) * | 1995-10-27 | 1999-11-16 | Praecis Pharmaceuticals, Inc. | Modulators of β-amyloid peptide aggregation comprising D-amino acids |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5135736A (en) * | 1988-08-15 | 1992-08-04 | Neorx Corporation | Covalently-linked complexes and methods for enhanced cytotoxicity and imaging |
US5434050A (en) * | 1991-08-13 | 1995-07-18 | Regents Of The University Of Minnesota | Labelled β-amyloid peptide and methods of screening for Alzheimer's disease |
WO1993011155A1 (en) * | 1991-12-03 | 1993-06-10 | Proteus Molecular Design Limited | Fragments of prion proteins |
TW327194B (en) * | 1992-05-01 | 1998-02-21 | American Cyanamid Co | Novel amyloid precursor proteins and methods of using same |
US6696061B1 (en) * | 1992-08-11 | 2004-02-24 | President And Fellows Of Harvard College | Immunomodulatory peptides |
US6120765A (en) * | 1993-04-02 | 2000-09-19 | Shiseido Co. Ltd. | Urokinase plasminogen activator fragments |
US5470951A (en) * | 1993-09-29 | 1995-11-28 | City Of Hope | Peptides for antagonizing the effects of amyloid βprotein |
JP3542181B2 (en) * | 1994-10-21 | 2004-07-14 | 日本たばこ産業株式会社 | New protein |
EP0866805A1 (en) * | 1995-12-12 | 1998-09-30 | Karolinska Innovations AB | PEPTIDE BINDING THE KLVFF-SEQUENCE OF AMYLOID $g(b) |
-
1996
- 1996-04-10 US US08/630,645 patent/US5948763A/en not_active Expired - Lifetime
- 1996-06-06 AU AU61129/96A patent/AU715662B2/en not_active Ceased
- 1996-06-06 AT AT96918482T patent/ATE369379T1/en not_active IP Right Cessation
- 1996-06-06 WO PCT/US1996/010220 patent/WO1996039834A1/en active IP Right Grant
- 1996-06-06 EP EP96918482A patent/EP0843516B1/en not_active Expired - Lifetime
- 1996-06-06 CA CA002222690A patent/CA2222690A1/en not_active Abandoned
- 1996-06-06 DE DE69637199T patent/DE69637199T2/en not_active Expired - Lifetime
- 1996-06-06 JP JP50224597A patent/JP2001519753A/en active Pending
- 1996-12-12 US US08/766,596 patent/US6462171B1/en not_active Expired - Lifetime
-
2002
- 2002-09-06 US US10/235,483 patent/US20030087407A1/en not_active Abandoned
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5169933A (en) * | 1988-08-15 | 1992-12-08 | Neorx Corporation | Covalently-linked complexes and methods for enhanced cytotoxicity and imaging |
US5547931A (en) * | 1994-02-23 | 1996-08-20 | Immtech International Inc. | Methods of stimulatory thrombocytopoiesis using modified C-reactive protein |
US5935778A (en) * | 1995-02-09 | 1999-08-10 | Boehringer Mannheim Gmbh | Method for serological typing using type-specific antigens |
US5817626A (en) * | 1995-03-14 | 1998-10-06 | Praecis Pharmaceuticals Incorporated | Modulators of beta-amyloid peptide aggregation |
US5854215A (en) * | 1995-03-14 | 1998-12-29 | Praecis Pharmaceuticals Incorporated | Modulators of β-amyloid peptide aggregation |
US5854204A (en) * | 1995-03-14 | 1998-12-29 | Praecis Pharmaceuticals, Inc. | Aβ peptides that modulate β-amyloid aggregation |
US5985242A (en) * | 1995-10-27 | 1999-11-16 | Praecis Pharmaceuticals, Inc. | Modulators of β-amyloid peptide aggregation comprising D-amino acids |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060069058A1 (en) * | 1999-11-05 | 2006-03-30 | Axonyx, Inc. | Beta-sheet breaker peptide analogs that inhibit beta-pleated sheet formation in amyloid beta-peptide |
US20040121960A1 (en) * | 1999-11-05 | 2004-06-24 | Claudio Soto-Jara | Peptide analogs and mimetics suitable for in vivo use in the treatment of diseases associated with abnormal protein folding into amyloid, amyloid like deposits or beta sheet rich pathological precursor thereof |
US20080241165A1 (en) * | 2002-07-09 | 2008-10-02 | Crossbeta Biosciences B.V. | Cross-beta structure comprising amyloid-binding proteins and methods for detection of the cross-beta structure, for modulating cross-beta structures fiber formation and modulating cross-beta structure-mediated toxicity |
US20070003552A1 (en) * | 2002-07-09 | 2007-01-04 | Gebbink Martijn F B | Cross-beta structure comprising amyloid binding proteins and methods for detection of the cross-beta structure, for modulating cross-beta structures fibril formation and for modulating cross-beta structure-mediated toxicity and method for interfering with blood coagulation |
US8158585B2 (en) | 2002-07-09 | 2012-04-17 | Crossbeta Biosciences B.V. | Cross-β structure comprising amyloid-binding proteins and methods for detection of the cross-β structure, for modulating cross-β structures fiber formation and modulating cross-β structure-mediated toxicity |
US8067187B2 (en) | 2005-07-13 | 2011-11-29 | Crossbeta Biosciences B.V. | Cross-β structure binding compounds |
US20070015206A1 (en) * | 2005-07-13 | 2007-01-18 | Umc Utrecht Holding B.V. | Method for detecting and/or removing protien comprising a cross-beta structure from a pharmaceutical composition |
US20080267948A1 (en) * | 2005-07-13 | 2008-10-30 | Martijn Frans Ben Gerard Gebbink | Croos-B Structure Binding Compounds |
US20070015133A1 (en) * | 2005-07-13 | 2007-01-18 | Umc Utrecht Holding B.V. | Method for detecting and/or removing protein and/or peptide comprising a cross-beta structure from an aqueous solution comprising a protein |
US8114832B2 (en) | 2005-07-13 | 2012-02-14 | Crossbeta Biosciences B.V. | Method for detecting and/or removing a protein comprising a cross-beta structure from a pharmaceutical composition |
US20080118529A1 (en) * | 2005-07-13 | 2008-05-22 | Gebbink Martijn Frans Ben Gera | Adjuvation Through Cross -Beta Structure |
US20090155254A1 (en) * | 2006-02-16 | 2009-06-18 | Martijn Frans Ben Gerard Gebbink | Affinity Regions |
US20100291090A1 (en) * | 2007-04-26 | 2010-11-18 | Strittmatter Stephen M | Prion Protein as a Receptor for Amyloid-Beta Oligomers |
EP2152744A4 (en) * | 2007-04-26 | 2012-02-15 | Univ Yale | PRION PROTEIN AS RECEPTOR FOR AMYLOID BETA OLIGOMERS |
WO2008134034A1 (en) * | 2007-04-26 | 2008-11-06 | Yale University | Prion protein as a receptor for amyloid-beta oligomers |
US9217036B2 (en) | 2007-04-26 | 2015-12-22 | Yale University | Prion protein as a receptor for amyloid-β oligomers |
US20110008376A1 (en) * | 2007-11-08 | 2011-01-13 | Martijn Frans Ben Gerard Gebbink | Immunogenic compositions capable of activating t-cells |
US20110052564A1 (en) * | 2007-11-08 | 2011-03-03 | Martijn Frans Ben Gerard Gebbink | Enhancement of immunogenicity of antigens |
US20090142377A1 (en) * | 2007-11-08 | 2009-06-04 | Crossbeta Biosciences B.V. | Immunogenic compositions |
US20100099609A1 (en) * | 2008-07-28 | 2010-04-22 | Buck Institute For Age Research | eAPP AND DERIVATIVES FOR TREATMENT OF ALZHEIMER'S DISEASE |
US10808034B2 (en) | 2016-04-15 | 2020-10-20 | Medimmune Limited | Anti-PrP antibodies and uses thereof |
US12110336B2 (en) | 2016-04-15 | 2024-10-08 | Medimmune Limited | Method for treating a neurodegenerative disease by administering an anti-cellular prion protein (PrPc) antibody |
Also Published As
Publication number | Publication date |
---|---|
ATE369379T1 (en) | 2007-08-15 |
US6462171B1 (en) | 2002-10-08 |
EP0843516A4 (en) | 2002-08-14 |
EP0843516B1 (en) | 2007-08-08 |
AU6112996A (en) | 1996-12-30 |
WO1996039834A1 (en) | 1996-12-19 |
DE69637199T2 (en) | 2008-04-24 |
CA2222690A1 (en) | 1996-12-19 |
EP0843516A1 (en) | 1998-05-27 |
DE69637199D1 (en) | 2007-09-20 |
JP2001519753A (en) | 2001-10-23 |
US5948763A (en) | 1999-09-07 |
AU715662B2 (en) | 2000-02-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6462171B1 (en) | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits | |
Estrada et al. | Disrupting β-amyloid aggregation for Alzheimer disease treatment | |
Fraser et al. | Fibril formation by primate, rodent, and Dutch-hemorrhagic analogs of Alzheimer amyloid. beta.-protein | |
Teplow | Structural and kinetic features of amyloid β-protein fibrillogenesis | |
Soto | Unfolding the role of protein misfolding in neurodegenerative diseases | |
Wilhelmus et al. | Small heat shock proteins inhibit amyloid-β protein aggregation and cerebrovascular amyloid-β protein toxicity | |
Hamley | The amyloid beta peptide: a chemist’s perspective. Role in Alzheimer’s and fibrillization | |
Fraser et al. | α1‐Antichymotrypsin binding to Alzheimer Aβ peptides is sequence specific and induces fibril disaggregation in vitro | |
Kisilevsky et al. | AßT Amyloidogenesis: Unique, or Variation on a Systemic Theme | |
JP5221633B2 (en) | Low molecular weight peptides for the treatment of Alzheimer's disease and other β-amyloid protein fibril formation disorders | |
Carter | The Interaction of Amyloid-β with ApoE: The form of beta amyloid is a partial determinant of the interaction with Apolipoprotein E | |
Sian et al. | Oligomerization of β-amyloid of the Alzheimer’s and the Dutch-cerebral-haemorrhage types | |
US20060069058A1 (en) | Beta-sheet breaker peptide analogs that inhibit beta-pleated sheet formation in amyloid beta-peptide | |
JP2004502781A (en) | Methods for preventing damage to nervous tissue and treating α-synuclein disease | |
KR20020079731A (en) | Peptide Analogs and Mimetics Suitable for in Vivo Use in the Treatment of Diseases Associated with Abnormal Protein Folding into Amyloid, Amyloid-like Deposits or β-Sheet Rich Pathological Precursor Thereof | |
Niu et al. | Aggregation Mechanisms and Molecular Structures of Amyloid‐β in Alzheimer's Disease | |
Bett et al. | Structure− activity relationships in peptide modulators of β-amyloid protein aggregation: variation in α, α-disubstitution results in altered aggregate size and morphology | |
US20020132758A1 (en) | Method for identifying compounds to treat medical pathologies associated with molecular crystallization | |
Matsunaga et al. | Conformational changes preceding amyloid-fibril formation of amyloid-beta and stefin B; parallels in pH dependence | |
US8003612B2 (en) | Small peptides for the treatment of Alzheimer's disease and other beta-amyloid protein disorders | |
Estrada et al. | Protein misfolding disorders and rational design of antimisfolding agents | |
Bugiani et al. | Preamyloid deposits, amyloid deposits, and senile plaques in Alzheimer's disease, Down syndrome, and aging | |
US9809627B2 (en) | Cyclized transthyretin peptide and methods of use therefor | |
Kim | Characterization of beta-amyloid aggregation and its modulation | |
Kremer | Interactions between beta-amyloid peptide and model neuronal membranes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |
|
AS | Assignment |
Owner name: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF Free format text: EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE;ASSIGNOR:NEW YORK UNIVERSITY;REEL/FRAME:020929/0072 Effective date: 20030521 |