Hadravová Romana, Rumlová Michaela, Ruml Tomáš
Institute of Organic Chemistry and Biochemistry IOCB Research Centre & Gilead Sciences, Academy of Sciences of the Czech Republic, Flemingovo nám. 2, 166 10 Prague, Czech Republic.
Institute of Organic Chemistry and Biochemistry IOCB Research Centre & Gilead Sciences, Academy of Sciences of the Czech Republic, Flemingovo nám. 2, 166 10 Prague, Czech Republic; Department of Biotechnology, University of Chemistry and Technology, Prague, Technická 5, 166 28 Prague, Czech Republic.
Virology. 2015 Dec;486:78-87. doi: 10.1016/j.virol.2015.08.029. Epub 2015 Sep 26.
Due to the high number of drug-resistant HIV-1 mutants generated by highly active antiretroviral therapy (HAART), there is continuing demand for new types of inhibitors. Both the assembly of the Gag polyprotein into immature and mature HIV-1 particles are attractive candidates for the blocking of the retroviral life cycle. Currently, no therapeutically-used assembly inhibitor is available. One possible explanation is the lack of a reliable and simple assembly inhibitor screening method. To identify compounds potentially inhibiting the formation of both types of HIV-1 particles, we developed a new fluorescent high-throughput screening assay. This assay is based on the quantification of the assembly efficiency in vitro in a 96-well plate format. The key components of the assay are HIV-1 Gag-derived proteins and a dual-labelled oligonucleotide, which emits fluorescence only when the assembly of retroviral particles is inhibited. The method was validated using three (CAI, BM2, PF74) reported assembly inhibitors.
由于高效抗逆转录病毒疗法(HAART)产生的耐药性HIV-1突变体数量众多,对新型抑制剂的需求持续存在。将Gag多蛋白组装成未成熟和成熟的HIV-1颗粒都是阻断逆转录病毒生命周期的有吸引力的候选靶点。目前,尚无用于治疗的组装抑制剂。一种可能的解释是缺乏可靠且简单的组装抑制剂筛选方法。为了鉴定可能抑制两种类型HIV-1颗粒形成的化合物,我们开发了一种新的荧光高通量筛选测定法。该测定法基于在96孔板形式下体外组装效率的定量。该测定法的关键成分是HIV-1 Gag衍生蛋白和一种双标记寡核苷酸,其仅在逆转录病毒颗粒组装受到抑制时才发出荧光。该方法使用三种(CAI、BM2、PF74)已报道的组装抑制剂进行了验证。