3bw9: Difference between revisions

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{{STRUCTURE_3bw9|  PDB=3bw9  |  SCENE=  }}  
{{STRUCTURE_3bw9|  PDB=3bw9  |  SCENE=  }}  


'''Crystal Structure of HLA B*3508 in complex with a HCMV 12-mer peptide from the pp65 protein'''
===Crystal Structure of HLA B*3508 in complex with a HCMV 12-mer peptide from the pp65 protein===




==Overview==
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CD8(+) T-cell responses to persistent viral infections are characterized by the accumulation of an oligoclonal T-cell repertoire and a reduction in the naive T-cell pool. However, the precise mechanism for this phenomenon remains elusive. Here we show that human cytomegalovirus (HCMV)-specific CD8(+) T cells recognizing distinct epitopes from the pp65 protein and restricted through an identical HLA class I allele (HLA B*3508) exhibited either a highly conserved public T-cell repertoire or a private, diverse T-cell response, which was uniquely altered in each donor following in vitro antigen exposure. Selection of a public T-cell receptor (TCR) was coincident with an atypical major histocompatibility complex (MHC)-peptide structure, in that the epitope adopted a helical conformation that bulged from the peptide-binding groove, while a diverse TCR profile was observed in response to the epitope that formed a flatter, more "featureless" landscape. Clonotypes with biased TCR usage demonstrated more efficient recognition of virus-infected cells, a greater CD8 dependency, and were more terminally differentiated in their phenotype when compared with the T cells expressing diverse TCR. These findings provide new insights into our understanding on how the biology of antigen presentation in addition to the structural features of the pMHC-I might shape the T-cell repertoire and its phenotype.
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==About this Structure==
==About this Structure==
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[[Category: Viral matrix protein]]
[[Category: Viral matrix protein]]
[[Category: Virion]]
[[Category: Virion]]
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