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8D5Q

TCR TG6 in complex with Ld-HF10

Summary for 8D5Q
Entry DOI10.2210/pdb8d5q/pdb
Related6X2T 6X30
DescriptorTCR-alpha, TCR-beta, H-2 class I histocompatibility antigen, L-D alpha chain, ... (7 entities in total)
Functional Keywordsmhci, cd8 t cell, immune system
Biological sourceMus musculus (Mouse)
More
Total number of polymer chains4
Total formula weight73728.58
Authors
Wang, Y.,Dai, S. (deposition date: 2022-06-05, release date: 2022-09-14, Last modification date: 2024-11-13)
Primary citationWang, Y.,Tsitsiklis, A.,Devoe, S.,Gao, W.,Chu, H.H.,Zhang, Y.,Li, W.,Wong, W.K.,Deane, C.M.,Neau, D.,Slansky, J.E.,Thomas, P.G.,Robey, E.A.,Dai, S.
Peptide Centric V beta Specific Germline Contacts Shape a Specialist T Cell Response.
Front Immunol, 13:847092-847092, 2022
Cited by
PubMed Abstract: Certain CD8 T cell responses are particularly effective at controlling infection, as exemplified by elite control of HIV in individuals harboring HLA-B57. To understand the structural features that contribute to CD8 T cell elite control, we focused on a strongly protective CD8 T cell response directed against a parasite-derived peptide (HF10) presented by an atypical MHC-I molecule, H-2Ld. This response exhibits a focused TCR repertoire dominated by Vβ2, and a representative TCR (TG6) in complex with Ld-HF10 reveals an unusual structure in which both MHC and TCR contribute extensively to peptide specificity, along with a parallel footprint of TCR on its pMHC ligand. The parallel footprint is a common feature of Vβ2-containing TCRs and correlates with an unusual Vα-Vβ interface, CDR loop conformations, and Vβ2-specific germline contacts with peptides. Vβ2 and Ld may represent "specialist" components for antigen recognition that allows for particularly strong and focused T cell responses.
PubMed: 35967379
DOI: 10.3389/fimmu.2022.847092
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.501 Å)
Structure validation

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