Knight D M, Flomerfelt F A, Ghrayeb J
Science. 1987 May 15;236(4803):837-40. doi: 10.1126/science.3033827.
The art/trs transactivator protein of human immunodeficiency virus (HIV) was expressed in mammalian cells as a 19-kilodalton protein that was immunoreactive with sera from HIV-infected patients. Separate plasmids encoding the art/trs protein, the tat protein, or the envelope glycoprotein gp120 were used to demonstrate that both art/trs and tat are absolutely required for the synthesis of gp120 from its cognate messenger RNA. In addition, both the tat and art/trs proteins influence the level of envelope RNA. The results suggest that art/trs and tat may be ideal targets for potential anti-HIV agents in AIDS therapy.
人类免疫缺陷病毒(HIV)的反式激活调节蛋白(art/trs)在哺乳动物细胞中表达为一种19千道尔顿的蛋白质,它能与HIV感染患者的血清发生免疫反应。分别使用编码art/trs蛋白、tat蛋白或包膜糖蛋白gp120的质粒来证明,从其同源信使核糖核酸合成gp120绝对需要art/trs和tat。此外,tat蛋白和art/trs蛋白都影响包膜RNA的水平。结果表明,art/trs和tat可能是艾滋病治疗中潜在抗HIV药物的理想靶点。