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利用MHC等位基因特异性基序精确预测流感病毒NS1蛋白中Kk限制的细胞毒性T细胞表位。

Precise prediction of a Kk-restricted cytotoxic T cell epitope in the NS1 protein of influenza virus using an MHC allele-specific motif.

作者信息

Cossins J, Gould K G, Smith M, Driscoll P, Brownlee G G

机构信息

Sir William Dunn School of Pathology, University of Oxford, United Kingdom.

出版信息

Virology. 1993 Mar;193(1):289-95. doi: 10.1006/viro.1993.1124.

Abstract

The nonstructural protein NS1 of influenza A/PR/8/34 virus has previously been reported to be recognized by murine Kk-restricted cytotoxic T lymphocytes (CTL), although the sequence of the epitope was not defined. A Kk-specific motif has previously been published and consists of a glutamic acid or (less frequently) an aspartic acid at position 2 and an isoleucine at the carboxyl terminus of a peptide eight or nine residues long. This motif was used here to predict the sequence of the NS1 epitope, which was defined as a nonapeptide corresponding to amino acid residues 152-160, sequence EEGAIVGEI. This is the first CTL epitope to be defined within the NS1 protein of the influenza A virus. A model of how this epitope could bind to the Kk molecule was produced by homology modelling from an X-ray crystal structure of a human HLA/peptide complex.

摘要

之前有报道称,甲型流感病毒A/PR/8/34的非结构蛋白NS1可被小鼠Kk限制性细胞毒性T淋巴细胞(CTL)识别,不过其表位序列尚未明确。此前已公布了一个Kk特异性基序,该基序在长度为8或9个残基的肽段中,第2位为谷氨酸或(较少见的)天冬氨酸,且在肽段的羧基末端为异亮氨酸。在此处,该基序被用于预测NS1表位的序列,其被定义为对应于氨基酸残基152 - 160的九肽,序列为EEGAIVGEI。这是在甲型流感病毒NS1蛋白中确定的首个CTL表位。通过对人HLA/肽复合物的X射线晶体结构进行同源建模,构建了该表位与Kk分子结合方式的模型。

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