Luukkonen B G, Fenyö E M, Schwartz S
Microbiology and Tumorbiology Center, Karolinska Institute, Stockholm, Sweden.
Virology. 1995 Feb 1;206(2):854-65. doi: 10.1006/viro.1995.1008.
Here we have investigated if human immunodeficiency virus type 1 (HIV-1) protease expressed in trans can interfere with production of infectious HIV-1 particles. Protease produced from a Tat and Rev inducible expression plasmid specifically cleaved HIV-1 p55Gag in a dose-dependent manner. Coexpression of protease and an infectious HIV-1 proviral clone resulted in increased intracellular cleavage of p55Gag. As a consequence, virus production and virus infectivity was significantly reduced. These results suggest that overexpression of HIV-1 protease in HIV-1-infected cells is a powerful way to inhibit production of infectious virions.
在此,我们研究了反式表达的1型人类免疫缺陷病毒(HIV-1)蛋白酶是否会干扰传染性HIV-1颗粒的产生。从Tat和Rev诱导型表达质粒产生的蛋白酶以剂量依赖的方式特异性切割HIV-1 p55Gag。蛋白酶与传染性HIV-1前病毒克隆的共表达导致p55Gag在细胞内的切割增加。结果,病毒产生和病毒感染性显著降低。这些结果表明,在HIV-1感染的细胞中过表达HIV-1蛋白酶是抑制传染性病毒粒子产生的有效方法。