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WO1998006440A3 - Phenotypic conversion of cells mediated by external guide sequences - Google Patents

Phenotypic conversion of cells mediated by external guide sequences Download PDF

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Publication number
WO1998006440A3
WO1998006440A3 PCT/US1997/014457 US9714457W WO9806440A3 WO 1998006440 A3 WO1998006440 A3 WO 1998006440A3 US 9714457 W US9714457 W US 9714457W WO 9806440 A3 WO9806440 A3 WO 9806440A3
Authority
WO
WIPO (PCT)
Prior art keywords
cells
drug
external guide
guide sequences
sensitive
Prior art date
Application number
PCT/US1997/014457
Other languages
French (fr)
Other versions
WO1998006440A2 (en
Inventor
Garry B Takle
Allan R Goldberg
Shaji T George
Original Assignee
Innovir Lab Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Innovir Lab Inc filed Critical Innovir Lab Inc
Priority to AU39844/97A priority Critical patent/AU3984497A/en
Publication of WO1998006440A2 publication Critical patent/WO1998006440A2/en
Publication of WO1998006440A3 publication Critical patent/WO1998006440A3/en

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1137Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/11Antisense
    • C12N2310/111Antisense spanning the whole gene, or a large part of it
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/12Type of nucleic acid catalytic nucleic acids, e.g. ribozymes
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/12Type of nucleic acid catalytic nucleic acids, e.g. ribozymes
    • C12N2310/126Type of nucleic acid catalytic nucleic acids, e.g. ribozymes involving RNAse P
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/12Type of nucleic acid catalytic nucleic acids, e.g. ribozymes
    • C12N2310/127DNAzymes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Life Sciences & Earth Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Zoology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Virology (AREA)
  • Microbiology (AREA)
  • Plant Pathology (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Disclosed are a method and compositions for delivering nucleic acids to bacterial cells. The method does not require manipulation of the bacteria and is therefore particularly suited to delivery of nucleic acids to bacteria in natural environments, including inside animal bodies. The method generally involves conjugating the nucleic acid to be delivered with a cationic porphyrin and bringing the conjugate and the target bacterial cells into contact. Both the porphyrin and conjugated nucleic acid are taken up by the bacterial cells and the nucleic acid can then have a biological effect on the cells. Specifically disclosed is a method for converting drug-resistant bacterial cells to drug-sensitive cells by delivery of external guide sequences to the cells which then promote cleavage of RNA molecules involved in conferring the drug-resistant phenotype on the cells. The drug-resistant phenotype of the cells is thus converted to a drug-sensitive phenotype. The drug-sensitive cells are then susceptible to drug therapy. Also disclosed is a method and compositions for killing eukaryotic pathogens or converting drug-resistant eukaryotic cells to drug-sensitive cells. The method involves the delivery of external guide sequences, ribozymes, or vectors encoding external guide sequences or ribozymes, to eukaryotic cells. Preferred target eukaryotic cells for the disclosed method include algae, protozoa, fungi, slime mold, and cells of helminths.
PCT/US1997/014457 1996-08-16 1997-08-15 Phenotypic conversion of cells mediated by external guide sequences WO1998006440A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU39844/97A AU3984497A (en) 1996-08-16 1997-08-15 Phenotypic conversion of cells mediated by external guide sequences

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US2367596P 1996-08-16 1996-08-16
US60/023,675 1996-08-16

Publications (2)

Publication Number Publication Date
WO1998006440A2 WO1998006440A2 (en) 1998-02-19
WO1998006440A3 true WO1998006440A3 (en) 1998-06-25

Family

ID=21816556

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1997/014457 WO1998006440A2 (en) 1996-08-16 1997-08-15 Phenotypic conversion of cells mediated by external guide sequences

Country Status (2)

Country Link
AU (1) AU3984497A (en)
WO (1) WO1998006440A2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9912965D0 (en) * 1999-06-03 1999-08-04 Oxford Biomedica Ltd In vivo selection method

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993013740A2 (en) * 1991-12-31 1993-07-22 Worcester Foundation For Experimental Biology Antiparasitic oligonucleotides active against drug resistant malaria
WO1994012643A1 (en) * 1992-12-03 1994-06-09 Unisearch Ltd. Nucleotide sequence encoding carbamoyl phosphate synthetase ii
WO1995027480A1 (en) * 1994-04-12 1995-10-19 Innovir Laboratories, Inc. Heme-bearing microparticles for targeted delivery of drugs
WO1996008558A1 (en) * 1994-09-12 1996-03-21 City Of Hope Modulation of drug radiation resistant genes
WO1996021731A2 (en) * 1995-01-13 1996-07-18 Innovir Laboratories, Inc. Stabilized external guide sequences
WO1996021665A1 (en) * 1995-01-13 1996-07-18 Board Of Regents, The University Of Texas System Turcasarins, novel expanded porphyrins, and uses thereof
WO1997033622A2 (en) * 1996-03-14 1997-09-18 Innovir Laboratories, Inc. Delivery of nucleic acids by porphyrins

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993013740A2 (en) * 1991-12-31 1993-07-22 Worcester Foundation For Experimental Biology Antiparasitic oligonucleotides active against drug resistant malaria
WO1994012643A1 (en) * 1992-12-03 1994-06-09 Unisearch Ltd. Nucleotide sequence encoding carbamoyl phosphate synthetase ii
WO1995027480A1 (en) * 1994-04-12 1995-10-19 Innovir Laboratories, Inc. Heme-bearing microparticles for targeted delivery of drugs
WO1996008558A1 (en) * 1994-09-12 1996-03-21 City Of Hope Modulation of drug radiation resistant genes
WO1996021731A2 (en) * 1995-01-13 1996-07-18 Innovir Laboratories, Inc. Stabilized external guide sequences
WO1996021665A1 (en) * 1995-01-13 1996-07-18 Board Of Regents, The University Of Texas System Turcasarins, novel expanded porphyrins, and uses thereof
WO1997033622A2 (en) * 1996-03-14 1997-09-18 Innovir Laboratories, Inc. Delivery of nucleic acids by porphyrins

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
GUERRIER-TAKADA C ET AL: "Phenotypic conversion of drug - resistant bacteria to drug sensitivity.", PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, (1997 AUG 5) 94 (16) 8468-72., XP002052175 *
GUERRIER-TAKADA, C. ET AL.: "Artificial regulation of gene expression in Escherichia coli by RNase P", PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF USA., vol. 92, November 1995 (1995-11-01), WASHINGTON US, pages 11115 - 11119, XP002052174 *
HARTMANN R K ET AL: "TOWARDS A NEW CONCEPT OF GENE INACTIVATION: SPECIFIC RNA CLEAVAGE BY ENDOGENOUS RIBONUCLEASE P", BIOTECHNOLOGY ANNUAL REVIEW, vol. 1, 1995, pages 215 - 265, XP000609333 *
HIROSHI KIJIMA ET AL: "THERAPEUTIC APPLICATIONS OF RIBOZYMES", PHARMACOLOGY AND THERAPEUTICS, vol. 68, no. 2, 1995, pages 247 - 267, XP000612090 *
KOBAYASHI H ET AL: "Reversal of drug sensitivity in multidrug-resistant tumor cells by an MDR1 (PGY1) ribozyme.", CANCER RESEARCH, (1994 MAR 1) 54 (5) 1271-5., XP002062947 *
MERCHAT, M. ET AL.: "Meso-substituted cationic porphyrins as efficient photosensitizers of Gram-positive and Gram-negative bacteria", JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B: BIOLOGY, vol. 32, February 1996 (1996-02-01), pages 153-157, XP002052173 *

Also Published As

Publication number Publication date
AU3984497A (en) 1998-03-06
WO1998006440A2 (en) 1998-02-19

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