Focal adhesion kinase and paxillin bind to peptides mimicking beta integrin cytoplasmic domains
Autor: | Carol A. Otey, Jeffrey D. Hildebrand, J T Parsons, Michael D. Schaller |
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Rok vydání: | 1995 |
Předmět: |
Cytoplasm
Integrins animal structures Molecular Sequence Data PTK2 Integrin macromolecular substances Focal adhesion Actinin Integrin-linked kinase Amino Acid Sequence Cytoskeleton Paxillin Binding Sites biology Articles Cell Biology Protein-Tyrosine Kinases Phosphoproteins Receptor Insulin Cell biology Cytoskeletal Proteins Focal Adhesion Kinase 1 Focal Adhesion Protein-Tyrosine Kinases biology.protein Integrin beta 6 Signal transduction Peptides Cell Adhesion Molecules Protein Binding Signal Transduction Proto-oncogene tyrosine-protein kinase Src |
Zdroj: | The Journal of Cell Biology |
ISSN: | 1540-8140 0021-9525 |
DOI: | 10.1083/jcb.130.5.1181 |
Popis: | The integrins have recently been implicated in signal transduction. A likely mediator of integrin signaling is focal adhesion kinase (pp125FAK or FAK), a structurally distinct protein tyrosine kinase that becomes enzymatically activated upon engagement of integrins with their ligands. A second candidate signaling molecule is paxillin, a focal adhesion associated, cytoskeletal protein that coordinately becomes phosphorylated on tyrosine upon activation of pp125FAK. Paxillin physically complexes with two protein tyrosine kinases, pp60src and Csk (COOH-terminal src kinase), and the oncoprotein p47gag-crk, each of which could function as part of a paxillin signaling complex. Using an in vitro assay we have established that the cytoplasmic domain of the beta 1 integrin can bind to paxillin and pp125FAK from chicken embryo cell lysates. The NH2-terminal, noncatalytic domain of pp125FAK can bind directly to the cytoplasmic tail of beta 1 and recognizes integrin sequences distinct from those involved in binding to alpha-actinin. Paxillin binding is independent of pp125FAK binding despite the fact that both bind to the same region of beta 1. These results demonstrate that the cytoplasmic domain of the beta subunits of integrins contain binding sites for both signaling molecules and structural proteins suggesting that integrins can coordinate the generation of cytoplasmic signals in addition to their role in anchoring components of the cytoskeleton. |
Databáze: | OpenAIRE |
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