Robertson J M, Jensen P E, Evavold B D
Department of Microbiology and Immunology, Emory University, Atlanta, GA 30322, USA.
J Immunol. 2000 May 1;164(9):4706-12. doi: 10.4049/jimmunol.164.9.4706.
The OVA323-339 epitope recognized by DO11.10 (H-2d) and OT-II (H-2b) T cells was investigated using amino- and carboxy-terminal truncations to locate the approximate ends of the epitopes and single amino acid substitutions of OVA323-339 to identify critical TCR contact residues of the OVA323-339 peptide. DO11.10 and OT-II T cells are both specific for a C-terminal epitope whose core encompasses amino acids 329-337. Amino acid 333 was identified as the primary TCR contact residue for both cells, and amino acid 331 was found to be an important secondary TCR contact residue; however, the importance of other secondary TCR contact residues and peptide flanking residues differ between the cells. Additional OVA323-339-specific clones were generated that recognized epitopes found in the N-terminal end or in the center of the peptide. These findings indicate that OVA323-339 can be presented by I-Ad in at least three binding registers. This study highlights some of the complexities of peptide Ags such as OVA323-339, which contain a nested set of overlapping T cell epitopes and MHC binding registers.
利用氨基端和羧基端截短法来确定OVA323 - 339表位的大致末端,并通过OVA323 - 339的单个氨基酸替换来鉴定该肽段关键的TCR接触残基,以此研究DO11.10(H - 2d)和OT - II(H - 2b)T细胞所识别的OVA323 - 339表位。DO11.10和OT - II T细胞均对一个C端表位具有特异性,其核心包含氨基酸329 - 337。氨基酸333被确定为这两种细胞的主要TCR接触残基,氨基酸331被发现是一个重要的次要TCR接触残基;然而,其他次要TCR接触残基和肽段侧翼残基的重要性在这两种细胞之间存在差异。还产生了额外的OVA323 - 339特异性克隆,它们识别在肽段N端或中间发现的表位。这些发现表明OVA323 - 339可以由I - Ad以至少三种结合方式呈递。本研究突出了诸如OVA323 - 339这类肽抗原的一些复杂性,其包含一组嵌套的重叠T细胞表位和MHC结合方式。