The purpose of this study was to identify the binding site(s) within laminin for the alpha 3 beta 1 integrin receptor. It has been previously shown, using proteolytic fragments and anti-laminin antibodies, that the region in laminin for alpha 3 beta 1 integrin binding is localized to the carboxy-terminal region at the end of the long arm (Gehlsen, K. R., E. Engvall, K. Dickerson, W. S. Argraves, and E. Ruoslahti. 1989. J. Biol. Chem. 264:19034-19038; Tomaselli, K. J., D. E. Hall, L. T. Reichardt, L. A. Flier, K. R. Gehlsen, D. C. Turner, and S. Carbonetto. 1990. Neuron. 5:651-662). Using synthetic peptides, we have identified an amino acid sequence within the carboxy-terminal region of the laminin A chain that is recognized by the alpha 3 beta 1 integrin. The amino acid sequence represented by the synthetic peptide GD-6 (KQNCLSSRASFRGCVRNLRLSR residues numbered 3011 to 3032) of the globular domain of the murine A chain supports cell attachment and inhibits cell adhesion to laminin-coated surfaces. By affinity chromatography, peptide GD-6-Sepharose specifically bound solubilized alpha 3 beta 1 from extracts of surface-iodinated cells in a cation-dependent manner, while it did not bind other integrins. In addition, exogenous peptide GD-6 specifically eluted bound alpha 3 beta 1 from laminin-Sepharose columns but did not elute the alpha 3 beta 1 integrin from a fibronectin-Sepharose column. Using integrin subunit-specific monoclonal antibodies, only those antibodies against the alpha 3 and beta 1 subunits inhibited cell adhesion to peptide GD-6-coated surfaces. Finally, a polyclonal antibody made against peptide GD-6 reacted specifically with both murine and human laminin and significantly inhibited cell adhesion to laminin-coated surfaces but not those coated with other matrix proteins. These results identify the laminin A chain amino acid sequence of peptide GD-6 as representing a binding site in laminin for the alpha 3 beta 1 integrin.
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15 April 1992
Article|
April 15 1992
A synthetic peptide derived from the carboxy terminus of the laminin A chain represents a binding site for the alpha 3 beta 1 integrin
KR Gehlsen,
KR Gehlsen
California Institute for Biological Research, La Jolla 92037.
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P Sriramarao,
P Sriramarao
California Institute for Biological Research, La Jolla 92037.
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LT Furcht,
LT Furcht
California Institute for Biological Research, La Jolla 92037.
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AP Skubitz
AP Skubitz
California Institute for Biological Research, La Jolla 92037.
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KR Gehlsen
California Institute for Biological Research, La Jolla 92037.
P Sriramarao
California Institute for Biological Research, La Jolla 92037.
LT Furcht
California Institute for Biological Research, La Jolla 92037.
AP Skubitz
California Institute for Biological Research, La Jolla 92037.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1992) 117 (2): 449–459.
Citation
KR Gehlsen, P Sriramarao, LT Furcht, AP Skubitz; A synthetic peptide derived from the carboxy terminus of the laminin A chain represents a binding site for the alpha 3 beta 1 integrin. J Cell Biol 15 April 1992; 117 (2): 449–459. doi: https://doi.org/10.1083/jcb.117.2.449
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