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TCR Vα与MHC对接和CD8依赖性之间的相关性:对T细胞选择的影响。

A correlation between TCR Valpha docking on MHC and CD8 dependence: implications for T cell selection.

作者信息

Buslepp Jennifer, Wang Huanchen, Biddison William E, Appella Ettore, Collins Edward J

机构信息

Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Immunity. 2003 Oct;19(4):595-606. doi: 10.1016/s1074-7613(03)00269-3.

Abstract

T cell receptors (TCR) adopt a similar orientation when binding with major histocompatibility complex (MHC) molecules, yet the biological mechanism that generates this similar TCR orientation remains obscure. We show here the cocrystallographic structure of a mouse TCR bound to a human MHC molecule not seen by the TCR during thymic development. The orientation of this xenoreactive murine TCR atop human MHC deviates from the typical orientation more than any previously determined TCR/MHC structure. This unique orientation is solely due to the placement of the TCR Valpha domain on the MHC. In light of new information provided by this structure, we have reanalyzed the existing TCR/MHC cocrystal structures and discovered unique features of TCR Valpha domain position on class I MHC that correlate with CD8 dependence. Finally, we propose that the orientation seen in TCR recognition of MHC is a consequence of selection during T cell development.

摘要

T细胞受体(TCR)与主要组织相容性复合体(MHC)分子结合时采用相似的取向,但产生这种相似TCR取向的生物学机制仍不清楚。我们在此展示了一种小鼠TCR与人MHC分子的共晶体结构,该人MHC分子在胸腺发育过程中未被TCR识别。这种异种反应性小鼠TCR在人MHC上的取向比任何先前确定的TCR/MHC结构偏离典型取向的程度都更大。这种独特的取向完全是由于TCR的Vα结构域在MHC上的位置所致。根据该结构提供的新信息,我们重新分析了现有的TCR/MHC共晶体结构,并发现了I类MHC上TCR Vα结构域位置的独特特征,这些特征与CD8依赖性相关。最后,我们提出在T细胞发育过程中的选择导致了TCR识别MHC时所见的取向。

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