Overton H A, McMillan D J, Gridley S J, Brenner J, Redshaw S, Mills J S
Department of Chemotherapy Biology, Roche Products Ltd., Welwyn Garden City, Herts, U.K.
Virology. 1990 Nov;179(1):508-11. doi: 10.1016/0042-6822(90)90326-m.
The ability of two novel synthetic compounds to inhibit the HIV protease-mediated processing of HIV-1 precursor polyproteins was investigated in an in vitro gag-protease mixed lysate assay system and in an assay using recombinant baculoviruses engineered to express the HIV-1 gag and pol genes in cultured insect cells. With the in vitro mixed lysate assay we have shown that both compounds at 1 microM can completely inhibit the HIV-1 and HIV-2 protease-mediated release of p24 from the HIV-1 gag precursor at pH 5.5 and pH 7.0. In the intracellular baculovirus system these compounds were shown to inhibit the protease-mediated maturation of gag and also the excision of the protease moiety from its precursor.
在体外gag蛋白酶混合裂解物检测系统以及使用经基因工程改造以在培养的昆虫细胞中表达HIV-1 gag和pol基因的重组杆状病毒的检测中,研究了两种新型合成化合物抑制HIV蛋白酶介导的HIV-1前体多蛋白加工的能力。通过体外混合裂解物检测,我们发现这两种化合物在1 microM浓度下,在pH 5.5和pH 7.0时都能完全抑制HIV-1和HIV-2蛋白酶介导的p24从HIV-1 gag前体的释放。在细胞内杆状病毒系统中,这些化合物被证明可抑制蛋白酶介导的gag成熟以及蛋白酶部分从前体中的切除。