Sequential Interactions of the TCR with Two Distinct Cytoplasmic Tyrosine Kinases

Makio Iwashima(Howard Hughes Medical Institute), Bryan Irving(Howard Hughes Medical Institute), Nicolai S. C. van Oers(Howard Hughes Medical Institute), Andrew C. Chan(Howard Hughes Medical Institute), Arthur Weiss(Howard Hughes Medical Institute)
Science
February 25, 1994
Cited by 719

Abstract

The T cell antigen receptor (TCR) initiates signals by interacting with cytoplasmic protein tyrosine kinases (PTKs) through a 17-residue sequence motif [called the antigen recognition activation motif (ARAM)] that is contained in the TCR zeta and CD3 chains. TCR stimulation induces the tyrosine phosphorylation of several cellular substrates, including the ARAMs. Lck kinase activity is required for phosphorylation of two conserved tyrosine residues in an ARAM. This phosphorylation leads to the recruitment of a second cytoplasmic PTK, ZAP-70, through both of the ZAP-70 Src homology 2 domains and its phosphorylation. Thus, TCR signal transduction is initiated by the sequential interaction of two PTKs with TCR ARAMs.


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