Sequential Interactions of the TCR with Two Distinct Cytoplasmic Tyrosine Kinases
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作者:
Iwashima, Makio
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机构:Univ Calif San Francisco, Dept Med, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Iwashima, Makio
Irving, Bryan A.
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机构:Univ Calif San Francisco, Dept Med, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Irving, Bryan A.
van Oers, Nicolai S. C.
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机构:Univ Calif San Francisco, Dept Med, Howard Hughes Med Inst, San Francisco, CA 94143 USA
van Oers, Nicolai S. C.
Chan, Andrew C.
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机构:Univ Calif San Francisco, Dept Med, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Chan, Andrew C.
Weiss, Arthur
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Univ Calif San Francisco, Dept Med, Howard Hughes Med Inst, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Med, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Weiss, Arthur
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机构:
[1] Univ Calif San Francisco, Dept Med, Howard Hughes Med Inst, San Francisco, CA 94143 USA
The T cell antigen receptor (TCR) inihates 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 phosphoryiation 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 PTK.s with TCR ARAMs.