WO1997044357A1

WO1997044357A1 - Synthetic glucagon binding proteins

Info

Publication number: WO1997044357A1
Application number: PCT/US1997/008509
Authority: WO
Inventors: Margaret A. Cascieri; Gary G. Chicchi; Michael P. Graziano; Patricia J. Hey
Original assignee: Merck & Co., Inc.
Priority date: 1996-05-22
Filing date: 1997-05-19
Publication date: 1997-11-27
Also published as: JP2000512132A; CA2255541A1; EP0901503A1

Abstract

A synthetic human glucagon (hGlu) binding protein designated hGluΔ252-259 binding protein is cloned, expressed and used in an in vitro assay to screen for compounds that bind to the synthetic binding protein, including compounds that specifically stimulate or inhibit the binding of glucagon to the synthetic receptor. The invention includes the assay, the synthetic binding protein used in the assay, DNA encoding the synthetic binding protein, cells expressing the synthetic binding protein, and compounds identified through the use of the synthetic binding protein.

Description

TITLE OF THE INVENTION

SYNTHETIC GLUCAGON BINDING PROTEINS

CROSS-RELATED APPLICATION This is a continuation application of U.S. Serial No.

60/017,612, filed May 22, 1996 now pending.

BACKGROUND OF THE INVENTION

Glucagon is a major counterregulatory hormone that attenuates the inhibition of liver glucogenesis by insulin. Glucagon receptors are found primarily in liver, although their presence has been documented in kidney and adipose tissue. Type II diabetics have elevated levels of plasma glucagon and increased rates of hepatic glucose production. In fact, the rate of hepatic glucose production positively correlates with fasting blood glucose levels in type II diabetes.

Therefore, antagonists of glucagon have the potential to improve insulin responsiveness in the liver, decrease the rate of gluconeogenesis and lower the rate of hepatic glucose output resulting in a decrease in the levels of plasma glucose. Glucagon action is mediated by a G protein-coupled receptor that stimulates cyclic AMP accumulation via activation of Gs. G-protein coupled receptors are characterized by the ability of agonists to promote the formation of a high affinity ternary complex between the agonist, the receptor and the G-protein. The α subunit of the G- protein contains a guanine nucleotide binding site that, in the high affinity ternary [G protein-receptor-agonist] complex, is occupied by GDP. Ln the presence of physiological concentrations of GTP, the GDP molecule in the guanine nucleotide binding site of the G protein is displaced by a GTP molecule. The binding of GTP dissociates the a subunit of the G protein from its β and γ subunits and from the receptor, thereby activating the G-protein to stimulate downstream effectors (adenylyl cyclase in the case of the glucagon receptor) and propagating the intracellular signal. Thus, the ternary complex is transient in the presence of physiological concentrations of GTP. Because the affinity of the agonist for the receptor-G protein complex is higher than its affinity for the uncomplexed receptor, one consequence of the destabilization of the ternary complex is a reduction in the affinity of the receptor for the agonist. Thus, the affinity of agonists for G-protein coupled receptors is a function of the efficiency with which the receptor is coupled to the G-protein. In contrast, antagonists bind with the same affinity to the receptor in the presence or absence of G-protein coupling. G protein-coupled receptors such as the glucagon receptor are predicted to have seven transmembrane domains linked by hydrophilic loops. Extensive modeling and mutagenesis experiments show that the binding domain for small molecules is within the transmembrane helical domains, although peptide agonist binding also involves the hydrophilic extracellular domains. However, the intracellular loop domains are involved in coupling of receptor to G- proteins. Deletion of either the amino terminal or carboxyl terminal sections of the third intracellular loop led to loss of functional coupling of the β-adrenergic receptor to Gs. However, these altered receptors maintained high affinity for agonist. Subsequent amino acid replacements in the third intracellular loop confirmed the role of this region in G protein interaction.

A human glucagon receptor has been cloned and expressed (D. MacNeil et al., 1994, Bioch. Biophys. Res. Comm. 198:328-334). We have characterized a mutant of the human glucagon receptor in which residues 252 to 259 in the second intracellular loop are deleted. The mutant protein is designated hGluΔ252-259 binding protein. When hGluΔ252-259 binding protein is expressed in COS cells, glucagon does not stimulate cAMP accumulation, suggesting that the hGluΔ252-259 binding protein does not couple to Gs upon agonist binding. However, the hGluΔ252-259 binding protein has higher affinity for glucagon than the wild type receptor, suggesting that the mutation locks the hGluΔ252- 259 binding protein into a conformation with high affinity for agonist. Thus, hGluΔ252-259 binding protein is a high affinity glucagon binding protein that does not function as a glucagon receptor (ie., it does not transduce a signal).

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 shows the sequence of the intracellular domains of the human glucagon receptor and the position of the deletion in intracellular loop 2.

Figure 2 shows the effect of glucagon on cAMP synthesis in COS cells transiently expressing either the wild type glucagon receptor or the hGlu Δ252-259 binding protein.

Figure 3 shows 125ι_gi_ucag_0n binding to membranes from COS cells transiently expressing wild type glucagon receptor or the hGluΔ252-259 binding protein.

SUMMARY OF THE INVENTION

A synthetic human glucagon (hGlu) binding protein lacking amino acid residues 252 through 259 of the wild type human glucagon receptor (hGlu Δ252-259 binding protein) is cloned, expressed and used in an in vitro assay to screen for compounds that bind to the synthetic binding protein, including compounds that specifically stimulate or inhibit the high affinity binding of glucagon to the synthetic binding protein. The invention includes the assay, the synthetic binding protein used in the assay, DNA encoding the synthetic binding protein, cells expressing the synthetic binding protein, and compounds identified through the use of the synthetic binding protein.

DETAILED DESCRIPTION OF THE INVENTION

The human glucagon receptor (hGlu) was identified, cloned and expressed in cell cultures by the instant inventors.

Once the human glucagon receptor or hGluΔ252-259 binding protein is cloned and expressed in a non-human cell line, such as COS-7 cells or CHO cells, the recombinant proteins are free of other human proteins. The membranes from the recombinant cells expressing these proteins are then isolated according to methods known in the art and may be used in a variety of membrane associated binding assays. One example of such an assay is described by Wright and Rodbell (J. Biol. Chem. 254:268-269, 1979). Generally, a compound of interest is used to compete with the binding of a known, quantifiable glucagon receptor ligand. By increasing the amount of unlabeled test compound, the labeled compound is competed off the receptor or hGluΔ252-259 binding protein. From these experiments, an IC50 value for each test compound is determined.

Thus, according to this invention, a method is provided for identifying compounds that bind synthetic hGluΔ252-259 binding protein comprising the following steps:

(a) cloning the synthetic hGluΔ252-259 binding protein; (b) splicing the cloned hGluΔ252-259 binding protein into an expression vector to produce a construct such that the hGluΔ252-259 binding protein is operably linked to transcription and translation signals sufficient to induce expression of the binding protein upon introduction of the construct into a prokaryotic or eukaryotic cell; (c) introducing the construct into a prokaryotic or eukaryotic cell that does not express a glucagon receptor or binding protein in the absence of the introduced construct; and (d) incubating cells or membranes isolated from cells produced in step (c) with a quantifiable compound known to bind to human glucagon receptors, and subsequently adding test compounds at a range of concentrations so as to compete the quantifiable compound from the receptor, such that an IC50 for the test compound is obtained as the concentration of test compound at which 50% of the quantifiable compound becomes displaced from the receptor or binding protein.

Whereas glucagon has been shown to counter the inhibitory effect of insulin on liver glucogenesis, an antagonist of glucagon action discovered as described above would increase insulin sensitivity and would be useful in the treatment of diabetes.

The following examples are provided to further define the invention without, however, limiting the invention to the particulars of these examples.

EXAMPLE 1 Mutagenesis of a cloned human glucagon receptor was performed using the Bio-Rad Mutagene Phagemid In Vitro mutagenesis kit, version 2. The sequence of the wild type receptor was modified to produce the hGluΔ252-259 binding protein using the oligonucleotide primer 5' CTG TAC CTG CAC AAC GAG AGG AGC TTC TTC 3'

(SEQ ID NO:l). This primer sequence corresponds to nucleotides 739 through 753 and 778 through 792 of the coding sequence of the human glucagon receptor. The deletion (ie., nucleotides 754 through 777 of the coding sequence of the human glucagon receptor) was confirmed by sequencing. The cDNA was ligated into the vector PCI/neo for expression studies.

COS cells were transfected in T 175 flask monolayers using

10 μg cDNA and 8 mg DEAE-dextran in Dulbecco's modified Eagles medium containing 10% Nuserum and 100 μM chloroquine for two hours at 37°C in 5% Cθ2 incubation followed by two minute shock in

10% DMSO. Cells were maintained in fresh growth medium overnight then were harvested and seeded into T175 flasks for binding and 24- well dishes for cyclase activity measurement. After two days, cells were harvested from flasks using enzyme-free dissociation fluid, homogenized and the crude membrane pellet was recovered by centrifugation. 125ι_gi_ucag_0n (5ft pM) binding to the membrane preparation was measured in 20mM Tris pH 7.4 containing 2.5 mM MgCl2, I mM DTT, 5 μg/ml leupeptin, 10 μg/ml benzamidine, 40 μg/ml bacitracin, 5 μg/ml soybean trypsin inhibitor and 3 μM o- phenanthroline +/- 1 μM glucagon for 1 hour. Bound cpm were recovered by filtration using aTomtec harvester and quantitfied in a gamma-scintillation counter. Functional responses in transfectants were measured by exposing the cell monolayers to Dulbecco's modified Eagles medium (basal), DMEM with increasing concentrations of glucagon or DMEM with 10 μM forskolin for thirty minutes at 22°C in order to generate intracellular cAMP. Cells were lysed in HCI and cAMP in lysates was acetylated and quantitated by radioimmunoassay. The amount of receptor protein in COS membranes was normalized by quantitating the binding of an antibody to the C-terminus of the glucagon receptor to a dot blot using various concentrations of membrane protein.

EXAMPLE 2 The sequence of the intracellular domains of the human glucagon receptor and the position of the deletion (Δ252-259) in intracellular loop 2 are shown in Figure 1. Expression of the wild type human glucagon receptor in COS cells produced an 8-fold increase in intracellular cAMP levels upon addition of glucagon (Figure 2). The EC50 for glucagon activation is 48 pM. Ln contrast, virtually no increase in cAMP levels is observed in cells expressing the hGluΔ252- 259 binding protein at up to 100 nM glucagon (Figure 2). These data were normalized for differences in expression levels of the two proteins as described below. These data suggest that the deletion of residues 252 to 259 in intracellular loop two of the human glucagon receptor disrupts the binding interaction between the receptor and Gs. Quantitation of the amount of human glucagon receptor or hGluΔ252-259 binding protein expressed in COS membranes was performed utilizing an antibody to the carboxyl terminal of the glucagon receptor. These experiments show that there is 38% higher expression of the wild type glucagon receptor than the hGluΔ252-259 binding protein in the transfection experiment shown in Figure 2.

Inhibition of the binding of 125ι_gi_ucag₀n to the wild type human glucagon receptor and hGluΔ252-259 binding protein by unlabeled glucagon shows that glucagon has a 4-fold higher affinity for the hGluΔ252-259 binding protein than for the wild type human glucagon receptor (Figure 3). Thus, despite the lack of coupling to Gs, the hGluΔ252-259 binding protein has high affinity for glucagon. Scatchard analysis of these data show that the binding of glucagon to the hGluΔ252-259 binding protein is fit to a single site with a Kd for glucagon of 0.7 nM. These data suggest that the deletion of residues 252 to 259 locks the protein into a conformation that has high affinity for agonist.

EXAMPLE 3 Compounds that bind synthetic hGluΔ252-259 binding protein are identified by a method such as:

(a) cloning the synthetic hGluΔ252-259 binding protein;

(b) splicing the cloned hGluΔ252-259 binding protein into an expression vector to produce a construct such that the hGluΔ252-259 binding protein is operably linked to transcription and translation signals sufficient to induce expression of the binding protein upon introduction of the construct into a prokaryotic or eukaryotic cell;

(c) introducing the construct into a prokaryotic or eukaryotic cell that does not express a glucagon receptor or binding protein in the absence of the introduced construct; and

(d) incubating cells or membranes isolated from cells produced in step (c) with a quantifiable compound known to bind to human glucagon receptors, and subsequently adding test compounds at a range of concentrations so as to compete the quantifiable compound from the receptor, such that an IC50 for the test compound is obtained as the concentration of test compound at which 50% of the quantifiable compound becomes displaced from the receptor or binding protein.

EXAMPLE 4 Compounds identified by the method of Example 3 are formulated into pharmaceutical compositions.

Claims

WHAT IS CLAIMED IS:

1. DNA encoding synthetic hGluRΔ252-259 binding protein.

2. The DNA molecule of Claim 1 , wherein the DNA coding for the binding protein is operably linked to regulatory sequences such that the binding protein may be expressed upon introduction into a prokaryotic or eukaryotic cell.

3. A peptide encoded by the DNA molecule of Claim 1.

4. A cell containing the DNA of Claim 1.

5. A method for identifying compounds that specifically bind to synthetic hGluΔ252-259 binding protein, comprising the steps of:

(a) cloning the synthetic binding protein;

(b) splicing the synthetic binding protein into an expression vector to produce a construct such that synthetic binding protein is operably linked to transcription and translation signals sufficient to induce expression of the binding protein upon introduction of the construct into a cell;

(c) introducing the construct into a prokaryotic or eukaryotic cell that does not express the glucagon receptor or synthetic binding protein in the absence of the introduced construct;

(d) incubating cells or membranes isolated from cells produced in step (c) with a quantifiable compound known to bind to human glucagon receptors or binding proteins, and subsequently adding test compounds at a range of concentrations so as to compete the quantifiable compound from the receptor or binding protein; and (e) calculating the relative binding affinity of the test compound to hGluΔ252-259 binding protein as expressed in the cells or membranes of step (d).

6. Compounds identified by the method of Claim 5.

7. A method of alleviating the effects of diabetes that comprises administering a pharmaceutically effective amount of a compound that specifically binds to the synthetic binding protein encoded by the DNA of Claim 1.

8. Synthetic human glucagon binding protein having the amino acid sequence shown in Figure 1.

9. Synthetic human glucagon binding protein designated hGluΔ252-259 binding protein.