Suppr超能文献

与MAGE-A4基因编码的肿瘤特异性抗原肽结合的HLA-A*0201的高分辨率结构。

High-resolution structure of HLA-A*0201 in complex with a tumour-specific antigenic peptide encoded by the MAGE-A4 gene.

作者信息

Hillig R C, Coulie P G, Stroobant V, Saenger W, Ziegler A, Hülsmeyer M

机构信息

Institut für Immungenetik, Universitätsklinikum Charité, Humboldt-Universität zu Berlin, Germany.

出版信息

J Mol Biol. 2001 Jul 27;310(5):1167-76. doi: 10.1006/jmbi.2001.4816.

Abstract

The heterotrimeric complex of the human major histocompatibity complex (MHC) molecule HLA-A0201, beta2-microglobulin and the decameric peptide GVYDGREHTV derived from the melanoma antigen (MAGE-A4 protein has been determined by X-ray crystallography at 1.4 A resolution. MAGE-A4 belongs to a family of genes that are specifically expressed in a variety of tumours. MAGE-A4-derived peptides are presented by MHC molecules at the cell surface to cytotoxic T-lymphocytes. As the HLA-A0201:MAGE-A4 complex occurs only on tumour cells, it is considered to be an appropriate target for immunotherapy. The structure presented here reveals potential epitopes specific to the complex and indicates which peptide residues could be recognised by T-cell receptors. In addition, as the structure could be refined anisotropically, it was possible to describe the movements of the bound peptide in more detail.

摘要

人类主要组织相容性复合体(MHC)分子HLA - A0201、β2 - 微球蛋白与源自黑色素瘤抗原(MAGE - A4蛋白)的十聚体肽GVYDGREHTV的异源三聚体复合物已通过X射线晶体学在1.4埃分辨率下确定。MAGE - A4属于在多种肿瘤中特异性表达的基因家族。MAGE - A4衍生的肽由MHC分子呈递至细胞表面给细胞毒性T淋巴细胞。由于HLA - A0201:MAGE - A4复合物仅出现在肿瘤细胞上,它被认为是免疫治疗的合适靶点。此处呈现的结构揭示了该复合物特有的潜在表位,并指出了哪些肽残基可被T细胞受体识别。此外,由于该结构可以进行各向异性精修,因此有可能更详细地描述结合肽的运动。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验