7Z0Q
MHC-II dynamics are maintained in HLA-DR allotypes to ensure catalyzed peptide exchange
Summary for 7Z0Q
Entry DOI | 10.2210/pdb7z0q/pdb |
Descriptor | HLA class II histocompatibility antigen, DR alpha chain, HLA-DRB1 protein, CLIP peptide, ... (5 entities in total) |
Functional Keywords | hla-drb1*0701, clip peptide, mhcii, immune system |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 3 |
Total formula weight | 47580.60 |
Authors | Roske, Y.,Abualrous, E.T.,Freund, C. (deposition date: 2022-02-23, release date: 2023-03-08, Last modification date: 2024-11-06) |
Primary citation | Abualrous, E.T.,Stolzenberg, S.,Sticht, J.,Wieczorek, M.,Roske, Y.,Gunther, M.,Dahn, S.,Boesen, B.B.,Calvo, M.M.,Biese, C.,Kuppler, F.,Medina-Garcia, A.,Alvaro-Benito, M.,Hofer, T.,Noe, F.,Freund, C. MHC-II dynamics are maintained in HLA-DR allotypes to ensure catalyzed peptide exchange. Nat.Chem.Biol., 19:1196-1204, 2023 Cited by PubMed Abstract: Presentation of antigenic peptides by major histocompatibility complex class II (MHC-II) proteins determines T helper cell reactivity. The MHC-II genetic locus displays a large degree of allelic polymorphism influencing the peptide repertoire presented by the resulting MHC-II protein allotypes. During antigen processing, the human leukocyte antigen (HLA) molecule HLA-DM (DM) encounters these distinct allotypes and catalyzes exchange of the placeholder peptide CLIP by exploiting dynamic features of MHC-II. Here, we investigate 12 highly abundant CLIP-bound HLA-DRB1 allotypes and correlate dynamics to catalysis by DM. Despite large differences in thermodynamic stability, peptide exchange rates fall into a target range that maintains DM responsiveness. A DM-susceptible conformation is conserved in MHC-II molecules, and allosteric coupling between polymorphic sites affects dynamic states that influence DM catalysis. As exemplified for rheumatoid arthritis, we postulate that intrinsic dynamic features of peptide-MHC-II complexes contribute to the association of individual MHC-II allotypes with autoimmune disease. PubMed: 37142807DOI: 10.1038/s41589-023-01316-3 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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