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- W2067328756 abstract "The interaction between the alphabeta T cell receptor (TCR) and the peptide bound to the major histocompatibility complex class I molecule (pMHC-I) constitutes a central interaction in adaptive immunity. How these receptors interact with such low affinity while maintaining exquisite specificity for peptide antigen and host MHC (MHC-I restriction) remains a challenge to be explained by structural immunologists. Moreover, how this extracellular interaction is transmitted as an intracellular signal via the CD3 complex remains unresolved. Nevertheless, several structures of TCRs, non-liganded and ligated to a defined pMHC-I, combined with detailed biophysical analyses, have provided insight of the structural basis of MHC-I restriction. In addition, structures of isolated CD3 components have enabled T cell signalling mechanisms to be postulated. Recent findings in this area, which include seven distinct TCR/pMHC-I complexes, have fundamental implications in adaptive immunity as well as therapeutic applications to modulate the adaptive immune response." @default.
- W2067328756 created "2016-06-24" @default.
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- W2067328756 date "2006-12-01" @default.
- W2067328756 modified "2023-10-16" @default.
- W2067328756 title "Specificity on a knife-edge: the αβ T cell receptor" @default.
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- W2067328756 doi "https://doi.org/10.1016/j.sbi.2006.09.004" @default.
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