Stebbins J, Deckman I C, Richardson S B, Debouck C
Department of Molecular Genetics, SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406, USA.
Anal Biochem. 1996 Nov 1;242(1):90-4. doi: 10.1006/abio.1996.0433.
A heterologous substrate assay for the human immunodeficiency virus type 1 (HIV-1) protease has been engineered in Escherichia coli. This assay detects the activity of the HIV-1 protease within intact bacterial cells and does not require biochemical purification of either the enzyme or the substrate. For this assay, nine HIV-1 protease specificity sites were genetically engineered into a heterologous protein (galactokinase) and the relative processing of these substrates by the wild-type and a substituted HIV-1 protease was determined. The results from these experiments revealed that the activity of the HIV-1 protease in the engineered heterologous substrate assay is consistent with previously reported in vitro assays and in vivo observations as well as a proposed catalytic specificity model.
一种用于人类免疫缺陷病毒1型(HIV-1)蛋白酶的异源底物检测方法已在大肠杆菌中构建成功。该检测方法可检测完整细菌细胞内HIV-1蛋白酶的活性,且无需对酶或底物进行生化纯化。在此检测方法中,九个HIV-1蛋白酶特异性位点被基因工程改造到一种异源蛋白(半乳糖激酶)中,并测定了野生型和一种替代型HIV-1蛋白酶对这些底物的相对加工情况。这些实验结果表明,在工程化异源底物检测中HIV-1蛋白酶的活性与先前报道的体外检测、体内观察结果以及提出的催化特异性模型一致。