Liu Zhen-long, Li Xiao-yu, Zhang Quan, Jia Ping-ping, Yang Liang, Wei Xiao-lu, Jiang Jian-dong, Cen Shan
Department of Immunology, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.
Yao Xue Xue Bao. 2010 Feb;45(2):257-62.
The HIV-1 Rev protein facilitates nuclear export of unspliced and singly spliced viral transcripts containing RRE RNA through the CRM1 export pathway. Inhibition of Rev-mediated RNA nuclear export can arrest HIV-1 transcriptional process, which clearly, reveals a target for anti-HIV drug development. In this work, a cell-based assay has been established for screening anti-HIV compounds targeting the Rev-mediated RNA nuclear export. This assay utilized a codon-optimized green fluorescent protein (GFP) as reporter gene, which expression is in a Rev-dependent manner. Any compound that inhibits the Rev-mediated RNA nuclear export is identified by reducing emission of GFP. The Z' score of this model is 0.8220. Three thousands compounds were screened and the positive rate was 9.3% with a cutoff at 50% inhibition. IMB7C7, one of the positive compounds, efficiently inhibits viral production from HIV-1 infected cells.
HIV-1 Rev蛋白通过CRM1输出途径促进含有RRE RNA的未剪接和单剪接病毒转录本的核输出。抑制Rev介导的RNA核输出可阻止HIV-1转录过程,这显然为抗HIV药物开发揭示了一个靶点。在这项工作中,已建立了一种基于细胞的检测方法,用于筛选靶向Rev介导的RNA核输出的抗HIV化合物。该检测方法利用密码子优化的绿色荧光蛋白(GFP)作为报告基因,其表达依赖于Rev。任何抑制Rev介导的RNA核输出的化合物都可通过降低GFP的发射来鉴定。该模型的Z'值为0.8220。筛选了3000种化合物,阳性率为9.3%,抑制率阈值为50%。阳性化合物之一IMB7C7可有效抑制HIV-1感染细胞中的病毒产生。