The adaptor protein Nck links receptor tyrosine kinases with the serine-threonine kinase Pak1

• Published in: The Journal of biological chemistry 1996-08, Vol.271 (35), p.20997-21000
• Main Authors: Galisteo, M L, Chernoff, J, Su, Y C, Skolnik, E Y, Schlessinger, J
• Format: Article
• Language: English
• Subjects: Adaptor Proteins, Signal Transducing; Amino Acid Sequence; Animals; Cell Line; ErbB Receptors - metabolism; HeLa Cells; Humans; Molecular Sequence Data; Oncogene Proteins - metabolism; p21-Activated Kinases; Protein Binding; Protein-Serine-Threonine Kinases - metabolism; Rats; Receptor Protein-Tyrosine Kinases - metabolism; Receptors, Platelet-Derived Growth Factor - metabolism; Signal Transduction
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.271.35.20997

Nck is an adaptor protein composed of a single SH2 domain and three SH3 domains. Upon growth factor stimulation, Nck is recruited to receptor tyrosine kinases via its SH2 domain, probably initiating one or more signaling cascades. In this report, we show that Nck is bound in living cells to the serine-threonine kinase Pak1. The association between Nck and Pak1 is mediated by the second SH3 domain of Nck and a proline-rich sequence in the amino terminus of Pak1. We also show that Pak1 is recruited by activated epidermal growth factor (EGF) and platelet-derived growth factor receptors. Moreover, Pak1 kinase activity is increased in response to EGF in HeLa cells transfected with human Pak1, and the kinase activity was enhanced when Nck was co-transfected. It is concluded that Nck links receptor tyrosine kinases with Pak1 and is probably involved in targeting and regulation of Pak1 activity.