Kim D W, Gwack Y, Han J H, Choe J
Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Taejon.
Biochem Biophys Res Commun. 1995 Oct 4;215(1):160-6. doi: 10.1006/bbrc.1995.2447.
The Hepatitis C Virus (HCV) NS3 protein contains amino acid motifs of a serine proteinase, a nucleotide triphosphatase (NTPase), and an RNA helicase based on amino acid sequence analysis. Proteinase and NTPase activities of the HCV NS3 protein were reported by several investigators. Here, we show that the recombinant HCV NS3 protein purified from a T7 promoter and His-tag expression system possesses an RNA helicase activity. The recombinant HCV NS3 protein consists of 466 amino acids from the carboxy terminal of a HCV NS3 open reading frame and 25 additional residues from the vector. The recombinant HCV NS3 protein was purified by metal-binding chromatography. The helicase activity requires ATP and divalent cations such as Mg2+ and Mn2+. The helicase activity was abolished by monoclonal antibody specific to the HCV NS3 protein.
基于氨基酸序列分析,丙型肝炎病毒(HCV)NS3蛋白含有丝氨酸蛋白酶、核苷酸三磷酸酶(NTPase)和RNA解旋酶的氨基酸基序。几位研究者报道了HCV NS3蛋白的蛋白酶和NTPase活性。在此,我们表明从T7启动子和His标签表达系统纯化的重组HCV NS3蛋白具有RNA解旋酶活性。重组HCV NS3蛋白由HCV NS3开放阅读框羧基末端的466个氨基酸和载体的另外25个残基组成。重组HCV NS3蛋白通过金属结合色谱法纯化。解旋酶活性需要ATP和二价阳离子,如Mg2+和Mn2+。HCV NS3蛋白特异性单克隆抗体可消除解旋酶活性。