High affinity integrin polypeptides and uses thereof

Chemistry: natural resins or derivatives; peptides or proteins; – Peptides of 3 to 100 amino acid residues – 25 or more amino acid residues in defined sequence

Reexamination Certificate

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Reexamination Certificate

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07064180

ABSTRACT:
Polypeptides comprising all or part of a variant integrin α subunit A domain or a variant integrin β subunit A-like domain are described. In solution or in membrane-associated form, the A domain or the A-like domain of the polypeptides of the invention exists predominantly in a high affinity conformation. In the polypeptides of the invention, referred to as variant integrin polypeptides, a crucial isoleucine residue (described in greater detail below) is absent. The isoleucine can be either deleted or replaced with different amino acids residue, preferably a smaller or less hydrophobic amino acid residue, e.g., alanine or glycine. Because the variant integrin polypeptides of the invention exist in solution or in membrane-associated form predominantly in a high affinity conformation, they are useful in screening assays for the identification of molecules that bind to (and/or mediate the activity of) an integrin. They are also useful for generating antibodies, e.g., monoclonal antibodies, which bind to the high affinity form of an integrin. Some such antibodies recognize an epitope that is either not present or not accessible on an integrin that is in a lower affinity conformation. The variant integrin polypeptides of the invention can be derived from any integrin α subunit or any integrin β subunit and could be used therapeutically. The variant integrin polypeptides preferably include a ligand-binding portion of an A-domain or an A-like domain.

REFERENCES:
patent: 5985278 (1999-11-01), Mitjans et al.
patent: 2003/0078375 (2003-04-01), Arnaout et al.
patent: WO 00/59878 (2000-10-01), None
patent: WO 00/60355 (2000-10-01), None
patent: WO 02/04521 (2002-01-01), None
patent: WO 02/31511 (2002-04-01), None
Burgess et al. Possible dissociation of the heparin-binding and mitogenic activities of heparin-binding . . . growth factor-1 from its receptor-binding activities by site-directed mutagenesis of a single lysine residue. J. Cell Biol. 1990, 111(5 Pt 1):2129-38.
Lazar et al. Transforming growth factor alpha: mutation of aspartic acid 47 and leucine 48 results in different biological activities. Mol Cell Biol. Mar. 8, 1988(3):1247-52.
Baldwin et al., “Cation binding to the integrin CD11b I domain and activation model assessment”,Structure, 6:923-935 (1998).
Edwards et al., “Mapping the Intercellular Adhesion Molecule-1 and -2 Binding Site on the Inserted Domain of Leukocyte Function-associated Antigen-1”,The Journal of Biological Chemistry, 273:28937-28944 (1998).
Emsley et al., “Structural Basis of Collagen Recognition by Integrin α2β1”,Cell, 100:47-56 (2000).
Emsley et al., “Crystal Structure of the I Domain from Integrin α2β1”,The Jounal of Biological Chemistry, 272:28512-28517 (1997).
Feng et al., “Peptides Derived from the Complementarity-determining Regions of Anti-Mac-1 Antibodies Block Intercellular Adhesion Molecule-1 Interaction with Mac-1”,The Jounal of Biological Chemistry, 273:5625-5630 (1998).
Kamata T and Takada Y, “Direct Binding of Collagen to the I Domain of Integrin α2β1 (VLA-2, CD49b/CD29) in a Divalent Cation-independent Manner”,The Journal of Biolocal Chemistry, 269:26006-26010 (1994).
Kern et al., “The Role of the I Domain in Ligand Binding of the Human Integrin α1β1”,The Journal of Biological Chemistry, 269:22811-22816 (1994).
Lee et al., “Crystal Structure of the A Domain from the α Subunit of Integrin CR3 (CD11b/CD18)”Cell, 80:631-638 (1995).
Lee et al., “Two conformations of the integrin A-domain (I-domain): a pathway for activation?”,Structure, 3:1333-1340 (1995).
Legge et al., “NMR Solution Structure of the Inserted Domain of Human Leukocyte Function Associated Antigen-1”,Journal of Molecular Biology, 295:1251-1264 (2000).
Li et al., “Two Functional States of the CD11b A-Domain: Correlations with Key Features of Two Mn2+-complexed Crystal Structures”,The Journal of Cell Biology, 143:1523-1534 (1998).
Michishita et al., “A Novel Divalent Cation-Binding Site in the A Domain of the β2 Integrin CR3 (CD11b/CD18) Is Essential for Ligand Binding”,Cell, 72:857-867 (1993).
Nolte et al., “Crystal structure of the α1β1 integrin I-domain: insights into integrin I-domain function”,FEBS Letters, 452:379-385 (1999).
Oxvig et al., “Conformational changes in tertiary structure near the ligand binding site of an integrin I domain”,Proc. Natl. Acad. Sci. USA, 96:2215-2220 (1999).
Rieu et al., “Solvent-accessible Residues on the Metal Ion-dependent Adhesion Site Face of Integrin CR3 Mediate Its Binding to the Neutrophil Inhibitory Factor”,The Journal of Biological Chemistry, 271:15858-15861 (1996).
Smith JW and Cheresh DA, “The Arg-Cly-Asp Binding Domain of the Vitronectin Receptor”,The Journal of Biological Chemistry, 263:18726-18731 (1988).
Zhang L and Plow EF, “A Discrete Site Modulates Activation of I Domains”,The Journal of Biological Chemistry, 271:29953-29957 (1996).
Zhang L and Plow EF, “Amino Acid Sequences within the α Subunit of Integrin αMβ2(Mac-1) Critical for Specific Recognition of C3bi”,Biochemistry, 38:8064-8071 (1999).
Xiong et al., “An Isoleucine-based Allosteric Switch Controls Affinity . . . ”0 J. of Biol. Chem. 275:38762-38767, 2000.
Burgess et al., “Possible Dissociation of the Heparin-Binding and Mitogenic Activities . . . ” J. Cell. Biol. 111:2129-2138, 1990.
Corbi et al., “The Human Leukocyte Adhesion Glycoprotein Mac-1 . . . ” J. Biol. Chem. 263(25):12403-11, 1988.
Huth et al., NMR and Mutagenesis Evidence for and I Domain Allosteric Site . . . : Proc. Nat;l. Acad. Sci. 97(10):5235, 2000.
Lazar et al., “Transforming Growth Factor Alpha: Mutation of Aspartic Acid 47 . . . ” Mol. Cell. Biol. 8:1247-1252, 1988.

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