Title of article :
What do TCR–pMHC crystal structures teach us about MHC restriction and alloreactivity?
Author/Authors :
Dominique Housset، نويسنده , , Bernard Malissen، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
9
From page :
429
To page :
437
Abstract :
MHC-encoded molecules govern immune responses by presenting antigenic peptides to T-cell receptors (TCRs). Several crystal structures of TCR–pMHC (peptide–MHC) complexes have unveiled the atomic details of this interaction, which is crucial to T-cell activation. By combining these data with biological and thermodynamical results, we revisit the structural basis of TCR crossreactivity and alloreactivity and the dynamics of the TCR binding process. Some emerging principles are at variance with recently proposed models of TCR recognition that would bring one back to ‘dual recognition’ models, in which TCR discriminates which part of its ligand is MHC and which part is peptide
Journal title :
Trends in Immunology
Serial Year :
2003
Journal title :
Trends in Immunology
Record number :
468774
Link To Document :
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