Kobori J A, Hood L, Shastri N
Division of Biology, California Institute of Technology, Pasadena 91125.
Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2940-4. doi: 10.1073/pnas.89.7.2940.
The alpha beta T-cell receptor (TCR) recognizes antigenic peptides bound to major histocompatibility complex (MHC) molecules. In contrast to the antibody combining site, for which the antigen contact or complementarity-determining residues (CDRs) have been precisely defined, the location and function of the corresponding CDR regions of the alpha and beta TCR chains are not known. To develop a model system for systematic analysis of the CDRs of the alpha beta TCR, we isolated a panel of murine T-cell clones that recognize a lysozyme peptide containing residues 74-88 bound to either Ab or Abm-12 MHC class II molecules. Although these two MHC molecules differ by only three amino acid residues within the A beta chain, each of the T-cell clones was specific for peptide bound to the self-MHC molecule and did not recognize the same peptide bound to the other MHC molecule. The structural basis for this exquisite ligand specificity of the TCRs was analyzed by isolation and characterization of alpha and beta chain genes from five closely related T-cell clones. Comparison of predicted amino acid sequences mapped the ligand specificity differences to residues present within the alpha chain variable region segment and the alpha and beta chain variable-joining region junction regions. Thus with current models of TCR-ligand interactions, the results suggest that residues 26-30 of the alpha chain variable region may constitute one of the CDR regions of the TCR.
αβ T细胞受体(TCR)识别与主要组织相容性复合体(MHC)分子结合的抗原肽。与抗体结合位点不同,抗体结合位点的抗原接触或互补决定残基(CDR)已被精确界定,而α和β TCR链相应CDR区域的位置和功能尚不清楚。为了开发一个用于系统分析αβ TCR的CDR的模型系统,我们分离了一组小鼠T细胞克隆,这些克隆识别与Ab或Abm-12 MHC II类分子结合的含有74 - 88位残基的溶菌酶肽。尽管这两种MHC分子在β链内仅相差三个氨基酸残基,但每个T细胞克隆都对与自身MHC分子结合的肽具有特异性,而不识别与另一种MHC分子结合的相同肽。通过从五个密切相关的T细胞克隆中分离和鉴定α链和β链基因,分析了TCR这种精细的配体特异性的结构基础。对预测氨基酸序列的比较将配体特异性差异定位到α链可变区片段以及α链和β链可变连接区连接区域内存在的残基上。因此,根据当前的TCR - 配体相互作用模型,结果表明α链可变区的26 - 30位残基可能构成TCR的一个CDR区域。