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HLA-A*0201限制性H-Y抗原含有一个翻译后修饰的半胱氨酸,该半胱氨酸显著影响T细胞识别。

The HLA-A*0201-restricted H-Y antigen contains a posttranslationally modified cysteine that significantly affects T cell recognition.

作者信息

Meadows L, Wang W, den Haan J M, Blokland E, Reinhardus C, Drijfhout J W, Shabanowitz J, Pierce R, Agulnik A I, Bishop C E, Hunt D F, Goulmy E, Engelhard V H

机构信息

Department of Chemistry, University of Virginia, Charlottesville 22901, USA.

出版信息

Immunity. 1997 Mar;6(3):273-81. doi: 10.1016/s1074-7613(00)80330-1.

Abstract

A peptide recognized by two cytotoxic T cell clones specific for the human minor histocompatibility antigen H-Y and restricted by HLA-A*0201 was identified. This peptide originates from SMCY, as do two other H-Y epitopes, supporting the importance of this protein as a major source of H-Y determinants in mice and humans. In naturally processed peptides, T cells only recognize posttranslationally altered forms of this peptide that have undergone modification of a cysteine residue in the seventh position. One of these modifications involves attachment of a second cysteine residue via a disulfide bond. This modification has profound effects on T cell recognition and also occurs in other class I MHC-associated peptides, supporting its general importance as an immunological determinant.

摘要

一种由两个针对人类次要组织相容性抗原H-Y且受HLA-A*0201限制的细胞毒性T细胞克隆识别的肽段被鉴定出来。该肽段源自SMCY,另外两个H-Y表位也是如此,这支持了该蛋白作为小鼠和人类中H-Y决定簇主要来源的重要性。在天然加工的肽段中,T细胞仅识别该肽段翻译后经修饰的形式,该修饰发生在第七位的半胱氨酸残基上。其中一种修饰涉及通过二硫键连接第二个半胱氨酸残基。这种修饰对T细胞识别有深远影响,并且也发生在其他I类MHC相关肽段中,支持了其作为免疫决定簇的普遍重要性。

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