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4H25

TCR interaction with peptide mimics of nickel offers structure insights to nickel contact allergy

Summary for 4H25
Entry DOI10.2210/pdb4h25/pdb
Related4H1L 4H26
DescriptorHLA class II histocompatibility antigen, DR alpha chain, MHC class II antigen, peptide, ... (6 entities in total)
Functional Keywordsprotein protein complex, immunoglobulin fold, antigen presentation, tcr, cell surface, immune system
Biological sourceHomo sapiens (human)
More
Total number of polymer chains6
Total formula weight93467.08
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 citationYin, 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: 23091041
DOI: 10.1073/pnas.1215928109
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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数据于2024-11-06公开中

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