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HLA-A2.4功能性变体KNE的结构分析。对HLA-A2特异性T细胞表位图谱绘制的意义。

Structural analysis of HLA-A2.4 functional variant KNE. Implications for the mapping of HLA-A2-specific T-cell epitopes.

作者信息

Doménech N, Ezquerra A, Castaño R, López de Castro J A

机构信息

Department of Immunology, Fundación Jiménez Díaz, Madrid, Spain.

出版信息

Immunogenetics. 1988;27(3):196-202. doi: 10.1007/BF00346586.

Abstract

HLA-A2 antigens are divided into four subtypes, designated A2.1 to A2.4, by the use of cytolytic T lymphocytes (CTL). The A2.4 subtype consists of a functionally heterogeneous group of variants that are not recognized by A2.1-, A2.2-, or A2.3-specific CTL lines while it is indistinguishable from A2.1 by isoelectric focusing. The structure of an A2.4 variant expressed on donor KNE has been established by comparative peptide mapping with A2.1 and radiochemical sequencing. It was found to differ from A2.1 by a single amino acid change of Cys to Tyr at position 99. This position is only moderately polymorphic and has not previously been found to vary in any other HLA or H-2 variants. The nature of the change is compatible with its generation by one-point mutation from A2.1. The only other previously characterized A2.4 variant, CLA, differs from A2.1 by a single amino acid replacement at position 9. Both residues 9 and 99 are located in homologous positions within the alpha 1 and alpha 2 domains, respectively. The results shown contribute to the molecular interpretation of the heterogeneity of CTL recognition within the HLA-A2.4 group of antigens.

摘要

通过使用细胞溶解性T淋巴细胞(CTL),HLA - A2抗原被分为四个亚型,命名为A2.1至A2.4。A2.4亚型由一组功能异质性的变体组成,这些变体不能被A2.1、A2.2或A2.3特异性CTL系识别,而通过等电聚焦它与A2.1无法区分。通过与A2.1进行比较肽图谱分析和放射化学测序,已确定了在供体KNE上表达的一种A2.4变体的结构。发现它与A2.1的区别在于第99位氨基酸由半胱氨酸(Cys)单氨基酸突变为酪氨酸(Tyr)。该位置仅有适度的多态性,此前在任何其他HLA或H - 2变体中均未发现其发生变化。这种变化的性质与其由A2.1的单点突变产生相一致。此前唯一另一个已被表征的A2.4变体CLA,与A2.1的区别在于第9位氨基酸的单氨基酸替换。第9位和第99位残基分别位于α1和α2结构域内的同源位置。所示结果有助于对HLA - A2.4组抗原内CTL识别异质性进行分子解释。

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