Machleidt W, Nägler D K, Assfalg-Machleidt I, Stubbs M T, Fritz H, Auerswald E A
Institut für Physiologische Chemie, Physikalische Biochemie und Zellbiologie der LMU München, Germany.
FEBS Lett. 1995 Mar 20;361(2-3):185-90. doi: 10.1016/0014-5793(95)00174-8.
Temporary inhibition of the cysteine proteinases papain and cathepsin L was observed with several hairpin loop mutants of recombinant chicken cystatin at enzyme concentrations above nanomolar. Kinetic modelling of inhibition data, gel electrophoresis and amino acid sequencing revealed that reappearance of papain activity is due to selective cleavage of the Gly(9)-Ala10 bond in the N-terminal binding area of the chicken cystatin variants, resulting in truncated inhibitors of lower affinity. Cleavage of the same bond by contaminating papaya proteinase IV was ruled out by previous purification of papain and suitable control experiments. According to the proposed kinetic model, cleavage occurs within the enzyme-inhibitor complex with first order rate constants ktemp of 2.3 x 10(-3) up to 5 x 10(-1) s-1. A similar ktemp/Km ratio was found for all mutants (0.7 x 10(6)-2.1 x 10(6) s-1.M-1); it is almost identical with the kcat/Km ratio of the peptide substrate Z-Phe-Arg-NHMec. These results suggest that distorted contacts of one of the hairpin loops affect binding of the N-terminal contact area in a way that covalent interaction of the Gly(9)-Ala10 bond with the active-site Cys residue of papain can occur and the bond is cleaved in a substrate-like manner.
在酶浓度高于纳摩尔时,观察到重组鸡半胱氨酸蛋白酶抑制剂的几种发夹环突变体对木瓜蛋白酶和组织蛋白酶L有暂时抑制作用。抑制数据的动力学建模、凝胶电泳和氨基酸测序表明,木瓜蛋白酶活性的重新出现是由于鸡半胱氨酸蛋白酶抑制剂变体N端结合区域的Gly(9)-Ala10键被选择性切割,导致亲和力较低的截短抑制剂。通过之前对木瓜蛋白酶的纯化和合适的对照实验排除了被污染的木瓜蛋白酶IV切割同一键的可能性。根据提出的动力学模型,切割发生在酶-抑制剂复合物内,一级速率常数ktemp为2.3×10(-3)至5×10(-1)s-1。所有突变体的ktemp/Km比值相似(0.7×10(6)-2.1×10(6)s-1·M-1);它几乎与肽底物Z-Phe-Arg-NHMec的kcat/Km比值相同。这些结果表明,一个发夹环的扭曲接触以某种方式影响N端接触区域的结合,使得Gly(9)-Ala10键与木瓜蛋白酶活性位点的半胱氨酸残基发生共价相互作用,并以类似底物的方式切割该键。