Trautwein K, Holliger P, Stackhouse J, Benner S A
Laboratory for Organic Chemistry, E.T.H. Zürich, Switzerland.
FEBS Lett. 1991 Apr 9;281(1-2):275-7. doi: 10.1016/0014-5793(91)80410-5.
Chemical modification studies suggest that two residues of bovine pancreatic ribonuclease A (RNase A), Lys-41 and Asp-121, are important for catalysis. Three mutants of RNase A have been prepared, two point mutants with Lys-41 altered to Arg-41 and Asp-121 altered to Glu-121, and a double mutant where both residues are altered. The Lys-41 Arg mutant has ca. 2% the catalytic activity (kcat/Km) of the native protein, while the Asp-121Glu mutant has ca. 17% the catalytic activity of the native protein. The double mutant has catalytic activity comparable to the Lys-41Arg mutant.
化学修饰研究表明,牛胰核糖核酸酶A(RNase A)的两个残基,即赖氨酸-41(Lys-41)和天冬氨酸-121(Asp-121),对催化作用很重要。已制备了三种RNase A突变体,两种单点突变体,其中赖氨酸-41变为精氨酸-41(Arg-41),天冬氨酸-121变为谷氨酸-121(Glu-121),以及一种两个残基都发生改变的双突变体。赖氨酸-41精氨酸突变体的催化活性(kcat/Km)约为天然蛋白质的2%,而天冬氨酸-121谷氨酸突变体的催化活性约为天然蛋白质的17%。双突变体的催化活性与赖氨酸-41精氨酸突变体相当。