Department of Biochemistry and Molecular Biology, School of Biomedical Sciences, Monash University, Clayton, Victoria 3800, Australia.
Nat Commun. 2013;4:2142. doi: 10.1038/ncomms3142.
The mucosal-associated invariant T-cell antigen receptor (MAIT TCR) recognizes MR1 presenting vitamin B metabolites. Here we describe the structures of a human MAIT TCR in complex with human MR1 presenting a non-stimulatory ligand derived from folic acid and an agonist ligand derived from a riboflavin metabolite. For both vitamin B antigens, the MAIT TCR docks in a conserved manner above MR1, thus acting as an innate-like pattern recognition receptor. The invariant MAIT TCR α-chain usage is attributable to MR1-mediated interactions that prise open the MR1 cleft to allow contact with the vitamin B metabolite. Although the non-stimulatory antigen does not contact the MAIT TCR, the stimulatory antigen does. This results in a higher affinity of the MAIT TCR for a stimulatory antigen in comparison with a non-stimulatory antigen. We formally demonstrate a structural basis for MAIT TCR recognition of vitamin B metabolites, while illuminating how TCRs recognize microbial metabolic signatures.
黏膜相关不变 T 细胞抗原受体(MAIT TCR)识别 MR1 呈递的维生素 B 代谢物。在这里,我们描述了人 MAIT TCR 与人 MR1 复合物的结构,MR1 呈递的非刺激性配体来源于叶酸,而激动剂配体来源于核黄素代谢物。对于这两种维生素 B 抗原,MAIT TCR 以保守的方式在 MR1 上方结合,因此作为一种先天样模式识别受体发挥作用。不变的 MAIT TCRα 链的使用归因于 MR1 介导的相互作用,这些相互作用使 MR1 裂隙张开,允许与维生素 B 代谢物接触。尽管非刺激性抗原不与 MAIT TCR 接触,但刺激性抗原会接触。这导致 MAIT TCR 对刺激性抗原的亲和力高于非刺激性抗原。我们正式证明了 MAIT TCR 识别维生素 B 代谢物的结构基础,同时阐明了 TCR 如何识别微生物的代谢特征。