Arginyl-glycyl-aspartic acid (RGD): a cell adhesion motif

SE D'Souza, MH Ginsberg, EF Plow - Trends in biochemical sciences, 1991 - Elsevier
SE D'Souza, MH Ginsberg, EF Plow
Trends in biochemical sciences, 1991Elsevier
Abstract The tripeptide Arg-Gly-Asp (RGD) was originally identified as the sequence within
fibronectin that mediates cell attachment. The RGD motif has now been found in numerous
other proteins and supports cell adhesion in many, but not all, of these. The integrins, a
family of cell-surface proteins, act as receptors for cell adhesion molecules. A subset of the
integrins recognize the RGD motif within their ligands, the binding of which mediates both
cell-substratum and cell-cell interactions. RGD peptides and mimetics, in addition to …
Abstract
The tripeptide Arg-Gly-Asp (RGD) was originally identified as the sequence within fibronectin that mediates cell attachment. The RGD motif has now been found in numerous other proteins and supports cell adhesion in many, but not all, of these. The integrins, a family of cell-surface proteins, act as receptors for cell adhesion molecules. A subset of the integrins recognize the RGD motif within their ligands, the binding of which mediates both cell-substratum and cell-cell interactions. RGD peptides and mimetics, in addition to providing insights into the fundamental mechanisms of cell adhesion, are potential therapeutic agents for the treatment of diseases such as thrombosis and cancer.
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