4H26
TCR interaction with peptide mimics of nickel offers structure insight to nickel contact allergy
Summary for 4H26
Entry DOI | 10.2210/pdb4h26/pdb |
Related | 4H1L 4H25 |
Descriptor | HLA class II histocompatibility antigen, DR alpha chain, MHC class II antigen, peptide, ... (5 entities in total) |
Functional Keywords | protein-protein complex, immunoglobulin fold, antigen presentation, tcr, cell surface, immune system |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 6 |
Total formula weight | 89258.38 |
Authors | Kappler, J.W.,Yin, L.,Dai, S.,Marrack, P.,Crawford, F. (deposition date: 2012-09-12, release date: 2013-10-16, Last modification date: 2024-11-06) |
Primary citation | Yin, L.,Crawford, F.,Marrack, P.,Kappler, J.W.,Dai, S. T-cell receptor (TCR) interaction with peptides that mimic nickel offers insight into nickel contact allergy. Proc.Natl.Acad.Sci.USA, 109:18517-18522, 2012 Cited by PubMed Abstract: T cell-mediated allergy to Ni(++) is one of the most common forms of allergic contact dermatitis, but how the T-cell receptor (TCR) recognizes Ni(++) is unknown. We studied a TCR from an allergic patient that recognizes Ni(++) bound to the MHCII molecule DR52c containing an unknown self-peptide. We identified mimotope peptides that can replace both the self-peptide and Ni(++) in this ligand. They share a p7 lysine whose εNH(2) group is surface-exposed when bound to DR52c. Whereas the TCR uses germ-line complementary-determining region (CDR)1/2 amino acids to dock in the conventional diagonal mode on the mimotope-DR52c complex, the interface is dominated by the TCR Vβ CDR3 interaction with the p7 lysine. Mutations in the TCR CDR loops have similar effects on the T-cell response to either the mimotope or Ni(++) ligand. We suggest that the mimotope p7 lysine mimics Ni(++) in the natural TCR ligand and that MHCII β-chain flexibility in the area around the peptide p7 position forms a common site for cation binding in metal allergies. PubMed: 23091041DOI: 10.1073/pnas.1215928109 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.5 Å) |
Structure validation
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