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Free Content Evidence for a human leucocyte antigen-DM-induced structural change in human leucocyte antigen-DOβ

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Summary

Human leucocyte antigen (HLA)-DO is a non-classical major histocompatibility complex class II molecule which modulates the function of HLA-DM and the loading of antigenic peptides on molecules such as HLA-DR. The bulk of HLA-DO associates with HLA-DM and this interaction is critical for HLA-DO egress from the endoplasmic reticulum. HLA-DM assists the early steps of HLA-DO maturation presumably through the stabilization of the interactions between the N-terminal regions of the α and β chains. To evaluate a possible role for HLA-DM in influencing the conformation of HLA-DO, we made use of a monoclonal antibody, Mags.DO5, that was raised against HLA-DO/DM complexes. Using transfected cells expressing mismatched heterodimers between HLA-DR and -DO chains, we found that the epitope for Mags.DO5 is located on the DOβ chain and that Mags.DO5 reactivity was increased upon cotransfection with HLA-DM. Our results suggest that HLA-DM influences the folding of HLA-DO in the endoplasmic reticulum. A mutant HLA-DO showing reduced capacity for endoplasmic reticulum egress was better recognized by Mags.DO5 in the presence of HLA-DM. On the other hand, an HLA-DO mutant capable of endoplasmic reticulum egress on its own was efficiently recognized by Mags.DO5, irrespective of the presence of HLA-DM. Taken together, our results suggest that HLA-DM acts as a private chaperone, directly assisting the folding of HLA-DO to promote egress from the endoplasmic reticulum.
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Keywords: B cells; antigen presentation; antigen processing; human; major histocompatibility complex

Document Type: Research Article

Affiliations: 1: Immunology Program, Weill Graduate School of Medical Sciences, Cornell University, and Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, NY, USA 2: Laboratoire d’Immunologie Moléculaire, Département de Microbiologie et Immunologie, Université de Montréal, Montréal, QC, Canada

Publication date: July 1, 2009

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