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7R7Z

Crystal structure of QW9-HLA-B*5301 specific T Cell Receptor, C3

Summary for 7R7Z
Entry DOI10.2210/pdb7r7z/pdb
DescriptorAlpha chain of C3 TCR, Beta chain of C3 TCR, SULFATE ION, ... (5 entities in total)
Functional Keywordsmhc, t cell immunity, antigen presentation, hiv, immune system
Biological sourceHomo sapiens (Human)
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Total number of polymer chains2
Total formula weight50591.89
Authors
Li, X.L.,Tan, K.M.,Xu, S.T.,Ng, R.,Walker, B.D.,Wang, J.H. (deposition date: 2021-06-25, release date: 2022-06-29, Last modification date: 2024-11-06)
Primary citationLi, X.,Singh, N.K.,Collins, D.R.,Ng, R.,Zhang, A.,Lamothe-Molina, P.A.,Shahinian, P.,Xu, S.,Tan, K.,Piechocka-Trocha, A.,Urbach, J.M.,Weber, J.K.,Gaiha, G.D.,Takou Mbah, O.C.,Huynh, T.,Cheever, S.,Chen, J.,Birnbaum, M.,Zhou, R.,Walker, B.D.,Wang, J.H.
Molecular basis of differential HLA class I-restricted T cell recognition of a highly networked HIV peptide.
Nat Commun, 14:2929-2929, 2023
Cited by
PubMed Abstract: Cytotoxic-T-lymphocyte (CTL) mediated control of HIV-1 is enhanced by targeting highly networked epitopes in complex with human-leukocyte-antigen-class-I (HLA-I). However, the extent to which the presenting HLA allele contributes to this process is unknown. Here we examine the CTL response to QW9, a highly networked epitope presented by the disease-protective HLA-B57 and disease-neutral HLA-B53. Despite robust targeting of QW9 in persons expressing either allele, T cell receptor (TCR) cross-recognition of the naturally occurring variant QW9_S3T is consistently reduced when presented by HLA-B53 but not by HLA-B57. Crystal structures show substantial conformational changes from QW9-HLA to QW9_S3T-HLA by both alleles. The TCR-QW9-B53 ternary complex structure manifests how the QW9-B53 can elicit effective CTLs and suggests sterically hindered cross-recognition by QW9_S3T-B53. We observe populations of cross-reactive TCRs for B57, but not B53 and also find greater peptide-HLA stability for B57 in comparison to B53. These data demonstrate differential impacts of HLAs on TCR cross-recognition and antigen presentation of a naturally arising variant, with important implications for vaccine design.
PubMed: 37217466
DOI: 10.1038/s41467-023-38573-8
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.286 Å)
Structure validation

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