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细胞毒性T淋巴细胞识别与HLA - A2相关的流感病毒基质蛋白片段。

Cytotoxic T lymphocytes recognize a fragment of influenza virus matrix protein in association with HLA-A2.

作者信息

Gotch F, Rothbard J, Howland K, Townsend A, McMichael A

出版信息

Nature. 1987;326(6116):881-2. doi: 10.1038/326881a0.

Abstract

Both human and murine cytotoxic T cells (CTL) elicited in response to infection with influenza A viruses have been shown to be specific for internal viral proteins, such as the matrix and nucleoprotein. Individual CTL epitopes have been identified in the nucleoprotein by successfully substituting short synthetic peptides for the intact virus in the preparation of target cells in cytotoxicity assays. The defined peptide epitopes have each been recognized by CTL in association with individual class I major histocompatibility complex (MHC) proteins, H-2Db, H-2Kk, H-2Kd (Taylor, P. et al., unpublished data) and HLA-B37. A logical strategy to investigate the molecular details of the interaction between antigen and MHC class I proteins would be to define an epitope recognized by the MHC class I molecule HLA-A2. This is because the amino-acid sequence is known, several variants of A2 have been characterized and the protein has been purified and crystallized. Here we describe a peptide derived from the influenza matrix protein that is recognized by human CTL in association with the HLA-A2 molecule.

摘要

对甲型流感病毒感染产生应答而引发的人类和鼠类细胞毒性T细胞(CTL)均已显示出对病毒内部蛋白具有特异性,如基质蛋白和核蛋白。通过在细胞毒性试验中制备靶细胞时成功用短合成肽替代完整病毒,已在核蛋白中鉴定出单个CTL表位。所确定的肽表位均已被CTL与单个I类主要组织相容性复合体(MHC)蛋白H-2Db、H-2Kk、H-2Kd(泰勒等人,未发表数据)和HLA-B37结合识别。研究抗原与I类MHC蛋白之间相互作用分子细节的一个合理策略是确定被I类MHC分子HLA-A2识别的表位。这是因为其氨基酸序列已知,已对A2的几种变体进行了表征,且该蛋白已被纯化和结晶。在此,我们描述了一种源自流感病毒基质蛋白的肽,它被人类CTL与HLA-A2分子结合识别。

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