T细胞受体
CD1D公司
抗原
细胞生物学
生物
T细胞
化学
免疫学
免疫系统
医学
作者
Adam P. Uldrich,Jérôme Le Nours,Daniel G. Pellicci,Nicholas A. Gherardin,Kirsty McPherson,Ricky Lim,Onisha Patel,Travis Beddoe,Stéphanie Gras,Jamie Rossjohn,Dale I. Godfrey
出处
期刊:Nature Immunology
[Springer Nature]
日期:2013-09-29
卷期号:14 (11): 1137-1145
被引量:253
摘要
The T cell repertoire comprises αβ and γδ T cell lineages. Although it is established how αβ T cell antigen receptors (TCRs) interact with antigen presented by antigen-presenting molecules, this is unknown for γδ TCRs. We describe a population of human V δ 1 + γδ T cells that exhibit autoreactivity to CD1d and provide a molecular basis for how a γδ TCR binds CD1d-α- galactosylceramide (α-GalCer). The γδ TCR docked orthogonally, over the A′ pocket of CD1d, in which the V δ 1-chain, and in particular the germ line-encoded CDR1δ loop, dominated interactions with CD1d. The TCR γ-chain sat peripherally to the interface, with the CDR3γ loop representing the principal determinant for α-GalCer specificity. Accordingly, we provide insight into how a γδ TCR binds specifically to a lipid-loaded antigen-presenting molecule.
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