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计算机模拟用于预测在受感染细胞中可能由HIV-1蛋白的蛋白水解作用产生的具有已知HLA I类基序的肽段的可用性。

Computer simulations to predict the availability of peptides with known HLA class I motifs possibly generated by proteolysis of HIV-1 proteins in infected cells.

作者信息

Becker Y

机构信息

Department of Molecular Virology, Faculty of Medicine, Hebrew University of Jerusalem, Israel.

出版信息

Virus Genes. 1995;10(3):227-37. doi: 10.1007/BF01701812.

Abstract

Cytotoxic T cells that recognize HIV-1 peptides generated from all viral proteins were reported. To predict the cleavage pattern of HIV-1 proteins by cytoplasmic proteasomes into peptides with motifs fitting known HLA class I molecules, the computer program Findpatterns was used. In this paper the combined amino acids patterns for proteolytic cleavages and the HLA class I haplotype-restricted peptides motifs are studied. It was noted that peptides with motifs of HLA class I A2 and A68 were abundant compared with HLA class 5B2, B8, B53, and B35.

摘要

据报道,存在能够识别由所有病毒蛋白产生的HIV-1肽段的细胞毒性T细胞。为了预测细胞质蛋白酶体将HIV-1蛋白切割成具有符合已知HLA I类分子基序的肽段的模式,使用了计算机程序Findpatterns。本文研究了蛋白水解切割的组合氨基酸模式以及HLA I类单倍型限制性肽基序。值得注意的是,与HLA 5B2、B8、B53和B35相比,具有HLA I类A2和A68基序的肽段更为丰富。

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