2nna
From Proteopedia
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Structure of the MHC class II molecule HLA-DQ8 bound with a deamidated gluten peptide
Overview
The risk of celiac disease is strongly associated with human leukocyte, antigen (HLA) DQ2 and to a lesser extent with HLA DQ8. Although the, pathogenesis of HLA-DQ2-mediated celiac disease is established, the, underlying basis for HLA-DQ8-mediated celiac disease remains unclear. We, showed that T helper 1 (Th1) responses in HLA-DQ8-associated celiac, pathology were indeed HLA DQ8 restricted and that multiple, mostly, deamidated peptides derived from protease-sensitive sites of gliadin were, recognized. This pattern of reactivity contrasted with the more absolute, deamidation dependence and relative protease resistance of the dominant, gliadin peptide in DQ2-mediated disease. We provided a structural basis, for the selection of HLA-DQ8-restricted, deamidated gliadin peptides. The, data established that the molecular mechanisms underlying HLA-DQ8-mediated, celiac disease differed markedly from the HLA-DQ2-mediated form of the, disease. Accordingly, nondietary therapeutic interventions in celiac, disease might need to be tailored to the genotype of the individual.
About this Structure
2NNA is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
A structural and immunological basis for the role of human leukocyte antigen DQ8 in celiac disease., Henderson KN, Tye-Din JA, Reid HH, Chen Z, Borg NA, Beissbarth T, Tatham A, Mannering SI, Purcell AW, Dudek NL, van Heel DA, McCluskey J, Rossjohn J, Anderson RP, Immunity. 2007 Jul;27(1):23-34. Epub 2007 Jul 12. PMID:17629515
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