HIV-1 gag proteins in virions and in infected cell fractions.

Biomedical science Pub Date : 1991-01-01
N K Sharova, V B Grigor'ev, A G Bukrinskaya
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Abstract

The relation of the initial products of the HIV-1 gag gene to the final products was determined in virus samples and cell fractions of infected H9 and Jurkat-tat cell cultures. The proteins were identified by immunoblotting with pooled sera from AIDS patients or monoclonal antibodies. The proportion in the virions of gag precursor proteins and the products of their proteolytic cleavage varied according to the maturity of the virus particles as determined by electron microscopy. The distribution of viral gag proteins in the cell fractions was determined 2, 4, and 24 h after infection. Treatment of cells with cycloheximide to block de novo protein synthesis did not significantly affect the results. Gag proteins containing the N terminus of the precursor p55 (including p55, the intermediate precursors p41(45) and p39, and mature protein p17) were found in the cell nuclei up to 24 h after infection. The major core protein p24 was located in the cytoplasmic fraction. These data strongly suggest that gag precursors from the p55 N terminus and the matrix protein p17 enter the infected cell separately from the major core protein p24, or become separated from it in the cytoplasm.

病毒粒子和感染细胞片段中的HIV-1 gag蛋白。
HIV-1 gag基因的初始产物与最终产物的关系是在病毒样本和感染H9和Jurkat-tat细胞培养的细胞组分中确定的。用艾滋病患者血清或单克隆抗体进行免疫印迹鉴定。病毒粒子中gag前体蛋白及其蛋白水解裂解产物的比例根据病毒粒子的成熟度而变化。感染后2、4、24 h检测病毒gag蛋白在细胞组分中的分布。用环己亚胺处理细胞以阻断新生蛋白合成对结果没有显著影响。感染24 h后,细胞核中发现含有前体p55 N端(包括p55、中间前体p41(45)和p39以及成熟蛋白p17)的Gag蛋白。主要核心蛋白p24位于细胞质部分。这些数据有力地表明,来自p55 N端和基质蛋白p17的gag前体与主要核心蛋白p24分开进入感染细胞,或在细胞质中与p24分离。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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