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激酶 Lck 如何磷酸化 T 细胞受体?空间组织作为一种调节机制。

How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism.

机构信息

Centre for Vascular Research, University of New South Wales, Sydney, NSW, Australia.

出版信息

Front Immunol. 2012 Jun 19;3:167. doi: 10.3389/fimmu.2012.00167. eCollection 2012.

Abstract

T cell signaling begins with the ligation of the T cell antigen receptor (TCR) by a cognate peptide and the phosphorylation of the receptor's immunoreceptor tyrosine-based activation motif domains by the kinase Lck. However, the canonical receptor model is insufficient to explain how the constitutively active kinase Lck can discriminate between non-ligated and ligated TCRs. Here, we discuss the factors that are thought to regulate the spatial distribution of the TCR and Lck, and therefore critically influence TCR signaling initiation.

摘要

T 细胞信号转导始于 T 细胞抗原受体(TCR)与同源肽的结合,以及激酶 Lck 对受体免疫受体酪氨酸激活基序域的磷酸化。然而,经典的受体模型不足以解释为什么组成性激活的激酶 Lck 能够区分非结合和结合的 TCR。在这里,我们讨论了被认为调节 TCR 和 Lck 空间分布的因素,这些因素对 TCR 信号转导的起始具有重要影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c211/3377954/3e8b268b0d6e/fimmu-03-00167-g001.jpg

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