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6EQA

HLA class I histocompatibility antigen

Summary for 6EQA
Entry DOI10.2210/pdb6eqa/pdb
Related3HG1
DescriptorHLA class I histocompatibility antigen, A-2 alpha chain, Beta-2-microglobulin, ALA-ALA-GLY-ILE-GLY-ILE-LEU-THR-VAL, ... (7 entities in total)
Functional Keywordsmelanoma, immune system, vaccine, tcr, mhc, 3d structure
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains5
Total formula weight93664.68
Authors
Rizkallah, P.J.,Cole, D.K. (deposition date: 2017-10-12, release date: 2018-10-10, Last modification date: 2024-11-13)
Primary citationMadura, F.,Rizkallah, P.J.,Legut, M.,Holland, C.J.,Fuller, A.,Bulek, A.,Schauenburg, A.J.,Trimby, A.,Hopkins, J.R.,Wells, S.A.,Godkin, A.,Miles, J.J.,Sami, M.,Li, Y.,Liddy, N.,Jakobsen, B.K.,Loveridge, E.J.,Cole, D.K.,Sewell, A.K.
TCR-induced alteration of primary MHC peptide anchor residue.
Eur.J.Immunol., 49:1052-1066, 2019
Cited by
PubMed Abstract: The HLA-A*02:01-restricted decapeptide EAAGIGILTV, derived from melanoma antigen recognized by T-cells-1 (MART-1) protein, represents one of the best-studied tumor associated T-cell epitopes, but clinical results targeting this peptide have been disappointing. This limitation may reflect the dominance of the nonapeptide, AAGIGILTV, at the melanoma cell surface. The decapeptide and nonapeptide are presented in distinct conformations by HLA-A*02:01 and TCRs from clinically relevant T-cell clones recognize the nonapeptide poorly. Here, we studied the MEL5 TCR that potently recognizes the nonapeptide. The structure of the MEL5-HLA-A*02:01-AAGIGILTV complex revealed an induced fit mechanism of antigen recognition involving altered peptide-MHC anchoring. This "flexing" at the TCR-peptide-MHC interface to accommodate the peptide antigen explains previously observed incongruences in this well-studied system and has important implications for future therapeutic approaches. Finally, this study expands upon the mechanisms by which molecular plasticity can influence antigen recognition by T cells.
PubMed: 31091334
DOI: 10.1002/eji.201948085
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.16 Å)
Structure validation

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