MHC-II dynamics are maintained in HLA-DR allotypes to ensure catalyzed peptide exchange
Authors
- E.T. Abualrous
- S. Stolzenberg
- J. Sticht
- M. Wieczorek
- Y. Roske
- M. Günther
- S. Dähn
- B.B. Boesen
- M.M. Calvo
- C. Biese
- F. Kuppler
- Á. Medina-García
- M. Álvaro-Benito
- T. Höfer
- F. Noé
- C. Freund
Journal
- Nature Chemical Biology
Citation
- Nat Chem Biol 19 (10): 1196-1204
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.