Abstract
Recognition by a T-cell antigen receptor (TCP) of peptide complexed with a major histo-compatibility complex (MHC) molecule occurs through variable loops in the TCP structure which bury almost all the available peptide and a much larger area of the MHC molecule. The TCP fits diagonally across the MHC peptide-binding site in a surface feature common to all class I and class II MHC molecules, providing evidence that the nature of binding is general. A broadly applicable binding mode has implications for the mechanism of repertoire selection and the magnitude of alloreactions.
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Garboczi, D., Ghosh, P., Utz, U. et al. Structure of the complex between human T-cell receptor, viral peptide and HLA-A2. Nature 384, 134–141 (1996). https://doi.org/10.1038/384134a0
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DOI: https://doi.org/10.1038/384134a0