Structural insight into MR1-mediated recognition of the mucosal associated invariant T cell receptor

• DOI: 10.1084/jem.20112095
• Publication Date: 2012-03-13T04:46:01Z
• Authors: Rangsima Reantragoon; Lars Kjer-Nielsen; Onisha Patel; Zhenjun Chen; Patricia T. Illing; Mugdha Bhati; Lyudmila Kostenko; Mandvi Bharadwaj; Bronwyn Meehan; Ted H. Hansen; Dale I. Godfrey; Jamie Rossjohn; James McCluskey
• Keywords: 570; Mucous Membrane; Histocompatibility Antigens Class I; Static Electricity; Receptors, Antigen, T-Cell; 610; CD1d; T-Cell; Complementarity Determining Regions; Article; Cell Line; Minor Histocompatibility Antigens; 03 medical and health sciences; 0302 clinical medicine; Antigen; Receptors; Humans; Natural Killer T-Cells; Antigens; Antigens, CD1d

Mucosal-associated invariant T (MAIT) cells express a semiinvariant αβ T cell receptor (TCR) that binds MHC class I–like molecule (MR1). However, the molecular basis for MAIT TCR recognition by MR1 is unknown. In this study, we present the crystal structure of a human Vα7.2Jα33-Vβ2 MAIT TCR. Mutagenesis revealed highly conserved requirements for the MAIT TCR–MR1 interaction across different human MAIT TCRs stimulated by distinct microbial sources. Individual residues within the MAIT TCR β chain were dispensable for the interaction with MR1, whereas the invariant MAIT TCR α chain controlled specificity through a small number of residues, which are conserved across species and located within the Vα-Jα regions. Mutagenesis of MR1 showed that only two residues, which were centrally positioned and on opposing sides of the antigen-binding cleft of MR1, were essential for MAIT cell activation. The mutagenesis data are consistent with a centrally located MAIT TCR–MR1 docking that was dominated by the α chain of the MAIT TCR. This candidate docking mode contrasts with that of the NKT TCR–CD1d-antigen interaction, in which both the α and β chain of the NKT TCR is required for ligation above the F′-pocket of CD1d.