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

机译:Lck激酶如何磷酸化T细胞受体?空间组织作为监管机制

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摘要

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.
机译:T细胞信号转导始于关联肽与T细胞抗原受体(TCR)的连接,以及激酶Lck对受体免疫受体基于酪氨酸的活化基序域的磷酸化。但是,规范的受体模型不足以解释组成型活性激酶Lck如何区分未连接的TCR和连接的TCR。在这里,我们讨论了被认为调节TCR和Lck的空间分布并因此严重影响TCR信号启动的因素。

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