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  • 标题:Differential thymic selection outcomes stimulated by focal structural alteration in peptide/major histocompatibility complex ligands
  • 本地全文:下载
  • 作者:Yoseph Ghendler ; Mai-kun Teng ; Jin-huan Liu
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:1998
  • 卷号:95
  • 期号:17
  • 页码:10061-10066
  • DOI:10.1073/pnas.95.17.10061
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:The T lineage repertoire is shaped by T cell receptor (TCR)-dependent positive and negative thymic selection processes. Using TCR-transgenic (N15tg) {beta}2-microglobulin-deficient ({beta}2m-/-) RAG-2-/- H-2b mice specific for the VSV8 (RGYVYQGL) octapeptide bound to Kb, we identified a single weak agonist peptide variant V4L (L4) inducing phenotypic and functional T cell maturation. The cognate VSV8 peptide, in contrast, triggers negative selection. The crystal structure of L4/Kb was determined and refined to 2.1 A for comparison with the VSV8/Kb structure at similar resolution. Aside from changes on the p4 side chain of L4 and the resulting alteration of the exposed Kb Lys-66 side chain, these two structures are essentially identical. Hence, a given TCR recognizes subtle distinctions between highly related ligands, resulting in dramatically different selection outcomes. Based on these finding and the recent structural elucidation of the N15-VSV8/Kb complex, moreover, it appears that the germ-line V repertoire contributes in a significant way to positive selection.
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