Crystal structure of an MHC class I presented glycopeptide that generates carbohydrate-specific CTL

被引:112
作者
Speir, JA
Abdel-Motal, UM
Jondal, M
Wilson, IA
机构
[1] Scripps Res Inst, Dept Biol Mol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[3] Karolinska Inst, Microbiol & Tumorbiol Ctr, S-17177 Stockholm, Sweden
关键词
D O I
10.1016/S1074-7613(00)80006-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell receptor (TCR) recognition of nonpeptidic and modified peptide antigens has been recently uncovered but is still poorly understood. Immunization with an H-2K(b)-restricted glycopeptide RGY8-6H-Gal(2) generates a population of cytotoxic T cells that express both alpha/beta TCR, specific for glycopeptide, and gamma/delta TCR, specific for the disaccharide, even on glycolipids, The crystal structure of K-b/RGY8-6H-Gal(2) now demonstrates that the peptide and H-2K(b) structures are unaffected by the peptide glycosylation, but the central region of the putative TCR binding site is dominated by the extensive exposure of the tethered carbohydrate. These features of the K-b/RGY8-6H-Gal(2) structure are consistent with the individual ligand binding preferences identified for the alpha/beta and gamma/delta TCRs and thus explain the generation of a carbohydrate-specific T cell response.
引用
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页码:51 / 61
页数:11
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