Fuse Takayuki, Watanabe Ken, Kitazato Kaio, Kobayashi Nobuyuki
Laboratory of Molecular Biology of Infectious Agents, Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki, Japan.
Microbes Infect. 2006 Jun;8(7):1783-9. doi: 10.1016/j.micinf.2006.02.016. Epub 2006 Apr 27.
The human immunodeficiency virus type 1 (HIV-1) protease (PR) plays an essential role in processing viral polyproteins into mature proteins. As a result, it is a major target for the development of drugs against AIDS. However, due to the rapid emergence of drug-resistant HIV, the development of novel HIV PR inhibitors is urgently needed. We recently established a new cell line E-PR293 which can be used as a safe, convenient and highly efficient assay system to screen HIV-1 PR inhibitors. In the cells, the HIV-1 PR is expressed in a chimeric protein with the green fluorescence protein (GFP). This assay measures the PR activity as a function of either the fluorescence of GFP or the cytotoxic activity of HIV-1 PR which is expressed in the cell. E-PR293 cells were maintained in the presence of doxycycline, which suppresses the expression of HIV-1 PR. The removal of doxycycline induces the expression of HIV-1 PR, which is used to screen HIV-1 PR inhibitors. In E-PR293 cells, the 50% inhibitory concentration of the cytotoxic effects by nelfinavir and saquinavir were as low as nanomolar levels, almost equal to those found in the HIV-infection assay.
1型人类免疫缺陷病毒(HIV-1)蛋白酶(PR)在将病毒多聚蛋白加工成成熟蛋白的过程中发挥着至关重要的作用。因此,它是抗艾滋病药物研发的主要靶点。然而,由于耐药性HIV的迅速出现,迫切需要开发新型HIV PR抑制剂。我们最近建立了一种新的细胞系E-PR293,它可作为一种安全、便捷且高效的检测系统来筛选HIV-1 PR抑制剂。在这些细胞中,HIV-1 PR与绿色荧光蛋白(GFP)以嵌合蛋白的形式表达。该检测通过GFP荧光或细胞中表达的HIV-1 PR的细胞毒性活性来衡量PR活性。E-PR293细胞在强力霉素存在的情况下进行培养,强力霉素可抑制HIV-1 PR的表达。去除强力霉素会诱导HIV-1 PR的表达,用于筛选HIV-1 PR抑制剂。在E-PR293细胞中,奈非那韦和沙奎那韦对细胞毒性作用的50%抑制浓度低至纳摩尔水平,几乎与HIV感染检测中的结果相当。