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ZAP-70对VHR磷酸酶的酪氨酸磷酸化作用。

Tyrosine phosphorylation of VHR phosphatase by ZAP-70.

作者信息

Alonso Andres, Rahmouni Souad, Williams Scott, van Stipdonk Marianne, Jaroszewski Lukasz, Godzik Adam, Abraham Robert T, Schoenberger Stephen P, Mustelin Tomas

机构信息

Program of Signal Transduction, The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Nat Immunol. 2003 Jan;4(1):44-8. doi: 10.1038/ni856. Epub 2002 Nov 25.

Abstract

The ZAP-70 tyrosine kinase is a key component of the signaling machinery for the T cell antigen receptor (TCR). Whereas recruitment and activation of ZAP-70 are relatively well understood, the proteins phosphorylated by ZAP-70 are incompletely known. We report here that VHR, a Vaccinia virus VH1-related dual-specific protein phosphatase that inactivates the mitogen-activated kinases Erk2 and Jnk, is phosphorylated at Y138 by ZAP-70. Tyr138 phosphorylation was required for VHR to inhibit the Erk2-Elk-1 pathway and, conversely, the VHR(Y138F) mutant augmented TCR-induced Erk2 kinase and activation of the gene encoding interleukin 2. These results suggest that VHR is a target for ZAP-70 and tempers activation of the Erk2 pathway in a ZAP-70-controlled manner.

摘要

ZAP-70酪氨酸激酶是T细胞抗原受体(TCR)信号传导机制的关键组成部分。虽然ZAP-70的募集和激活已得到较好理解,但其磷酸化的蛋白质仍不完全清楚。我们在此报告,痘苗病毒VH1相关双特异性蛋白磷酸酶VHR可使丝裂原活化激酶Erk2和Jnk失活,其在Y138位点被ZAP-70磷酸化。Y138磷酸化是VHR抑制Erk2-Elk-1途径所必需的,相反,VHR(Y138F)突变体增强了TCR诱导的Erk2激酶活性以及白细胞介素2编码基因的激活。这些结果表明VHR是ZAP-70的作用靶点,并以ZAP-70控制的方式调节Erk2途径的激活。

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