T细胞受体
磷酸化
免疫受体酪氨酸激活基序
酪氨酸磷酸化
原癌基因酪氨酸蛋白激酶Src
酪氨酸激酶
CD3型
细胞质
细胞生物学
生物
蛋白质酪氨酸磷酸酶
SH3域
受体酪氨酸激酶
SH2域
锡克
酪氨酸
化学
分子生物学
激酶
生物化学
T细胞
信号转导
抗原
遗传学
免疫系统
CD8型
作者
Makio Iwashima,Bryan Irving,Nicolai S. C. van Oers,Andrew C. Chan,Arthur Weiss
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1994-02-25
卷期号:263 (5150): 1136-1139
被引量:694
标识
DOI:10.1126/science.7509083
摘要
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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