Tözsér József, Tropea Joseph E, Cherry Scott, Bagossi Peter, Copeland Terry D, Wlodawer Alexander, Waugh David S
Department of Biochemistry and Molecular Biology, Research Center for Molecular Medicine, University of Debrecen, Debrecen, Hungary.
FEBS J. 2005 Jan;272(2):514-23. doi: 10.1111/j.1742-4658.2004.04493.x.
The substrate specificity of the nuclear inclusion protein a (NIa) proteolytic enzymes from two potyviruses, the tobacco etch virus (TEV) and tobacco vein mottling virus (TVMV), was compared using oligopeptide substrates. Mutations were introduced into TEV protease in an effort to identify key determinants of substrate specificity. The specificity of the mutant enzymes was assessed by using peptides with complementary substitutions. The crystal structure of TEV protease and a homology model of TVMV protease were used to interpret the kinetic data. A comparison of the two structures and the experimental data suggested that the differences in the specificity of the two enzymes may be mainly due to the variation in their S4 and S3 binding subsites. Two key residues predicted to be important for these differences were replaced in TEV protease with the corresponding residues of TVMV protease. Kinetic analyses of the mutants confirmed that these residues play a role in the specificity of the two enzymes. Additional residues in the substrate-binding subsites of TEV protease were also mutated in an effort to alter the specificity of the enzyme.
利用寡肽底物比较了两种马铃薯Y病毒(烟草蚀纹病毒(TEV)和烟草脉斑驳病毒(TVMV))的核内含体蛋白a(NIa)蛋白酶的底物特异性。对TEV蛋白酶进行了突变,以确定底物特异性的关键决定因素。通过使用具有互补取代的肽来评估突变酶的特异性。利用TEV蛋白酶的晶体结构和TVMV蛋白酶的同源模型来解释动力学数据。两种结构与实验数据的比较表明,两种酶特异性的差异可能主要归因于它们S4和S3结合亚位点的变化。预测对这些差异很重要的两个关键残基在TEV蛋白酶中被TVMV蛋白酶的相应残基取代。对突变体的动力学分析证实,这些残基在两种酶的特异性中起作用。为了改变酶的特异性,还对TEV蛋白酶底物结合亚位点中的其他残基进行了突变。