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一种基于报告基因的单步检测法,用于评估靶向HIV-1 Rev-RRE相互作用的抑制剂。

A reporter based single step assay for evaluation of inhibitors targeting HIV-1 Rev-RRE interaction.

作者信息

Raina Sumeer, Chande Ajit G, Baba Masanori, Mukhopadhyaya Robin

机构信息

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.

出版信息

Virusdisease. 2014 Jan;25(1):101-6. doi: 10.1007/s13337-013-0166-8. Epub 2013 Sep 27.

DOI:10.1007/s13337-013-0166-8
PMID:24426316
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3889232/
Abstract

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.

摘要

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。

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本文引用的文献

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Multiple platforms of a HIV-2 derived lentiviral vector for expanded utility.多种 HIV-2 衍生的慢病毒载体平台,具有广泛的应用。
Plasmid. 2013 Jan;69(1):90-5. doi: 10.1016/j.plasmid.2012.09.006. Epub 2012 Nov 15.
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Short communication: a single step assay for rapid evaluation of inhibitors targeting HIV type 1 Tat-mediated long terminal repeat transactivation.简短通讯:一种用于快速评估靶向HIV-1 Tat介导的长末端重复序列反式激活的抑制剂的单步检测法。
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Proflavine acts as a Rev inhibitor by targeting the high-affinity Rev binding site of the Rev responsive element of HIV-1.原黄素通过靶向HIV-1 Rev反应元件的高亲和力Rev结合位点来发挥Rev抑制剂的作用。
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AIDS Res Hum Retroviruses. 2002 Jul 1;18(10):705-9. doi: 10.1089/088922202760072320.
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Inhibition of the HIV-1 rev-RRE complex formation by unfused aromatic cations.未融合的芳香阳离子对HIV-1 rev-RRE复合物形成的抑制作用。
Bioorg Med Chem. 2001 May;9(5):1097-113. doi: 10.1016/s0968-0896(00)00344-8.
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Construction of peptides with nucleobase amino acids: design and synthesis of the nucleobase-conjugated peptides derived from HIV-1 Rev and their binding properties to HIV-1 RRE RNA.含核碱基氨基酸的肽的构建:源自HIV-1 Rev的核碱基共轭肽的设计与合成及其与HIV-1 RRE RNA的结合特性
Bioorg Med Chem. 2001 Apr;9(4):991-1000. doi: 10.1016/s0968-0896(00)00324-2.
10
Aminoglycoside antibiotics, neamine and its derivatives as potent inhibitors for the RNA-protein interactions derived from HIV-1 activators.氨基糖苷类抗生素、新霉素及其衍生物作为HIV-1激活剂来源的RNA-蛋白质相互作用的有效抑制剂。
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