Stone Jennifer D, Chervin Adam S, Kranz David M
Department of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Immunology. 2009 Feb;126(2):165-76. doi: 10.1111/j.1365-2567.2008.03015.x.
The interaction between the T-cell receptor (TCR) and its peptide-major histocompatibility complex (pepMHC) ligand plays a critical role in determining the activity and specificity of the T cell. The binding properties associated with these interactions have now been studied in many systems, providing a framework for a mechanistic understanding of the initial events that govern T-cell function. There have been various other reviews that have described the structural and biochemical features of TCR : pepMHC interactions. Here we provide an overview of four areas that directly impact our understanding of T-cell function, as viewed from the perspective of the TCR : pepMHC interaction: (1) relationships between T-cell activity and TCR : pepMHC binding parameters, (2) TCR affinity, avidity and clustering, (3) influence of coreceptors on pepMHC binding by TCRs and T-cell activity, and (4) impact of TCR binding affinity on antigenic peptide specificity.
T细胞受体(TCR)与其肽-主要组织相容性复合体(pepMHC)配体之间的相互作用在决定T细胞的活性和特异性方面起着关键作用。目前已在许多系统中研究了与这些相互作用相关的结合特性,为从机制上理解调控T细胞功能的初始事件提供了一个框架。已有各种其他综述描述了TCR:pepMHC相互作用的结构和生化特征。在此,我们从TCR:pepMHC相互作用的角度概述直接影响我们对T细胞功能理解的四个领域:(1)T细胞活性与TCR:pepMHC结合参数之间的关系,(2)TCR亲和力、亲合力和聚集,(3)共受体对TCR与pepMHC结合及T细胞活性的影响,以及(4)TCR结合亲和力对抗原肽特异性的影响。