Raina Sumeer, Chande Ajit G, Baba Masanori, Mukhopadhyaya Robin
Virology Laboratory, Advanced Centre for Treatment, Research and Education in Cancer (ACTREC), Tata Memorial Centre, Kharghar, Navi Mumbai, 410 210 India.
Virology Laboratory, Advanced Centre for Treatment, Research and Education in Cancer (ACTREC), Tata Memorial Centre, Kharghar, Navi Mumbai, 410 210 India ; Immunology Group, ICGEB, New Delhi, India.
Virusdisease. 2014 Jan;25(1):101-6. doi: 10.1007/s13337-013-0166-8. Epub 2013 Sep 27.
Human immunodeficiency virus regulatory protein Rev (regulator of viral expression) is translated from a monocistronic transcript produced early in the viral replication cycle. Rev binds to the cis-acting, highly structured viral RNA sequence Rev response element (RRE) and the Rev-RRE complex primarily controls nucleocytoplasmic transport of viral RNAs. Inhibition of Rev-RRE interaction therefore is an attractive target to block viral transport. We have developed a stable cell line carrying a lentiviral vector harboring a rev gene and a co-linear Rev-dependent GFP/luciferase reporter gene cassette and thus constitutively expressing the reporter proteins. Dose-dependent luciferase activity inhibition in the indicator cell line by known small molecule inhibitors Proflavin and K37 established the specificity of the assay. This novel single step assay, that involves use of very small amount of reagents/cells and addition of test material as the only manipulation, can therefore be useful for screening therapeutically potential Rev-RRE interaction inhibitors.
人类免疫缺陷病毒调节蛋白Rev(病毒表达调节因子)由病毒复制周期早期产生的单顺反子转录本翻译而来。Rev与顺式作用的、高度结构化的病毒RNA序列Rev反应元件(RRE)结合,Rev-RRE复合物主要控制病毒RNA的核质运输。因此,抑制Rev-RRE相互作用是阻断病毒运输的一个有吸引力的靶点。我们构建了一个稳定的细胞系,该细胞系携带一个含有rev基因和共线性Rev依赖性GFP/荧光素酶报告基因盒的慢病毒载体,从而组成性表达报告蛋白。已知小分子抑制剂普罗黄素和K37对指示细胞系中荧光素酶活性的剂量依赖性抑制确定了该检测方法的特异性。这种新颖的单步检测方法,只需使用极少量的试剂/细胞,且仅将测试材料的添加作为唯一操作,因此可用于筛选具有治疗潜力的Rev-RRE相互作用抑制剂。