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HLA-DM介导肽从HLA-DR上解离

Mediation by HLA-DM of dissociation of peptides from HLA-DR.

作者信息

Sloan V S, Cameron P, Porter G, Gammon M, Amaya M, Mellins E, Zaller D M

机构信息

Department of Autoimmune Disease Research, Merck Research Laboratories, Rahway, New Jersey 07065, USA.

出版信息

Nature. 1995 Jun 29;375(6534):802-6. doi: 10.1038/375802a0.

Abstract

Human leukocyte antigen (HLA)-DM is an unconventional major histocompatibility complex (MHC) class II heterodimer that is important for B-cell-mediated antigen processing and presentation to MHC class II-restricted T cells. HLA-DM is encoded by two genes, DMA and DMB, which map to the MHC class II region, and shares some homology with MHC class I and class II proteins. Here we define the biochemical role of HLA-DM. Recombinant soluble HLA-DM heterodimers have been purified from culture supernatants of insect cell transformants. At pH 5.0, they induce the dissociation of a subset of peptides bound to HLA-DR, including a nested set of class-II-associated invariant chain peptides (CLIP). This process liberates HLA-DR and leads to the enhanced binding of exogenous peptides.

摘要

人类白细胞抗原(HLA)-DM是一种非常规的主要组织相容性复合体(MHC)II类异二聚体,对于B细胞介导的抗原加工以及向MHC II类限制性T细胞呈递抗原有重要作用。HLA-DM由两个基因DMA和DMB编码,这两个基因定位于MHC II类区域,并且与MHC I类和II类蛋白具有一些同源性。在此我们确定了HLA-DM的生化作用。重组可溶性HLA-DM异二聚体已从昆虫细胞转化体的培养上清液中纯化出来。在pH 5.0时,它们可诱导与HLA-DR结合的一部分肽解离,包括一组嵌套的II类相关恒定链肽(CLIP)。这一过程释放出HLA-DR,并导致外源肽结合增强。

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