6VM8

SILv44 T cell receptor bound to HLA-A2 presenting gp100T2M peptide (IMDQVPFSV)

6VM8 の概要

• エントリーDOI: 10.2210/pdb6vm8/pdb
• 分子名称: MHC class I antigen, A-2 alpha chain, SILv44 T cell receptor beta chain, SILv44 T cell receptor alpha chain, ... (7 entities in total)
• 機能のキーワード: tcr, mhc class i, hla a2, autoimmune, vitiligo, melanoma, immune system
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 95937.69

構造登録者

Smith, A.R.,Baker, B.M. (登録日: 2020-01-27, 公開日: 2020-11-25, 最終更新日: 2024-10-30)

主引用文献

Smith, A.R.,Alonso, J.A.,Ayres, C.M.,Singh, N.K.,Hellman, L.M.,Baker, B.M.
Structurally silent peptide anchor modifications allosterically modulate T cell recognition in a receptor-dependent manner.
Proc.Natl.Acad.Sci.USA, 118:-, 2021

PubMed Abstract: Presentation of peptides by class I MHC proteins underlies T cell immune responses to pathogens and cancer. The association between peptide binding affinity and immunogenicity has led to the engineering of modified peptides with improved MHC binding, with the hope that these peptides would be useful for eliciting cross-reactive immune responses directed toward their weak binding, unmodified counterparts. Increasing evidence, however, indicates that T cell receptors (TCRs) can perceive such anchor-modified peptides differently than wild-type (WT) peptides, although the scope of discrimination is unclear. We show here that even modifications at primary anchors that have no discernible structural impact can lead to substantially stronger or weaker T cell recognition depending on the TCR. Surprisingly, the effect of peptide anchor modification can be sensed by a TCR at regions distant from the site of modification, indicating a through-protein mechanism in which the anchor residue serves as an allosteric modulator for TCR binding. Our findings emphasize caution in the use and interpretation of results from anchor-modified peptides and have implications for how anchor modifications are accounted for in other circumstances, such as predicting the immunogenicity of tumor neoantigens. Our data also highlight an important need to better understand the highly tunable dynamic nature of class I MHC proteins and the impact this has on various forms of immune recognition.

PubMed: 33468649
DOI: 10.1073/pnas.2018125118

実験手法

X-RAY DIFFRACTION (2.41 Å)