Hansson L O, Bolton-Grob R, Widersten M, Mannervik B
Department of Biochemistry, Uppsala University, Biomedical Center, Sweden.
Protein Sci. 1999 Dec;8(12):2742-50. doi: 10.1110/ps.8.12.2742.
Two human Mu class glutathione transferases, hGST M1-1 and hGST M2-2, with high sequence identity (84%) exhibit a 100-fold difference in activities with the substrates aminochrome, 2-cyano-1,3-dimethyl-1-nitrosoguanidine (cyanoDMNG), and 1,2-dichloro-4-nitrobenzene (DCNB), hGST M2-2 being more efficient. A sequence alignment with the rat Mu class GST M3-3, an enzyme also showing high activities with aminochrome and DCNB, demonstrated an identical structural cluster of residues 164-168 in the alpha6-helices of rGST M3-3 and hGST M2-2, a motif unique among known sequences of human, rat, and mouse Mu class GSTs. A putative electrostatic network Arg107-Asp161-Arg165-Glu164(-Gln167) was identified based on the published three-dimensional structure of hGST M2-2. Corresponding variant residues of hGSTM1-1 (Leu165, Asp164, and Arg167) as well as the active site residue Ser209 were targeted for point mutations, introducing hGST M2-2 residues to the framework of hGST M1-1, to improve the activities with substrates characteristic of hGST M2-2. In addition, chimeric enzymes composed of hGST M1-1 and hGST M2-2 sequences were analyzed. The activity with 1-chloro-2,4-dinitrobenzene (CDNB) was retained in all mutant enzymes, proving that they were catalytically competent, but none of the point mutations improved the activities with hGST M2-2 characteristic substrates. The chimeric enzymes showed that the structural determinants of these activities reside in domain II and that residue Arg165 in hGST M2-2 appears to be important for the reactions with cyanoDMNG and DCNB. A mutant, which contained all the hGST M2-2 residues of the putative electrostatic network, was still lacking one order of magnitude of the activities with the characteristic substrates of wild-type hGST M2-2. It was concluded that a limited set of point mutations is not sufficient, but that indirect secondary structural affects also contribute to the hGST M2-2 characteristic activities with aminochrome, cyanoDMNG, and DCNB.
两种人源 Mu 类谷胱甘肽转移酶 hGST M1-1 和 hGST M2-2,具有较高的序列同一性(84%),但在与氨基色素、2-氰基-1,3-二甲基-1-亚硝基胍(氰基 DMNG)和 1,2-二氯-4-硝基苯(DCNB)等底物的活性上存在 100 倍的差异,hGST M2-2 的效率更高。与大鼠 Mu 类 GST M3-3(一种对氨基色素和 DCNB 也表现出高活性的酶)进行序列比对,结果表明在 rGST M3-3 和 hGST M2-2 的α6 螺旋中,164 - 168 位残基存在相同的结构簇,这是在人、大鼠和小鼠 Mu 类 GST 的已知序列中独一无二的基序。基于已发表的 hGST M2-2 的三维结构,确定了一个假定的静电网络 Arg107 - Asp161 - Arg165 - Glu164(-Gln167)。hGSTM1-1 的相应变异残基(Leu165、Asp164 和 Arg167)以及活性位点残基 Ser209 被作为点突变的靶点,将 hGST M2-2 的残基引入 hGST M1-1 的框架中,以提高其对 hGST M2-2 特征性底物的活性。此外,还分析了由 hGST M1-1 和 hGST M2-2 序列组成的嵌合酶。所有突变酶都保留了对 1-氯-2,4-二硝基苯(CDNB)的活性,证明它们具有催化活性,但没有一个点突变能提高对 hGST M2-2 特征性底物的活性。嵌合酶表明这些活性的结构决定因素位于结构域 II,并且 hGST M2-2 中的 Arg165 残基似乎对与氰基 DMNG 和 DCNB 的反应很重要。一个包含假定静电网络所有 hGST M2-2 残基的突变体,与野生型 hGST M2-2 的特征性底物的活性仍相差一个数量级。得出的结论是,有限的一组点突变是不够的,而且间接的二级结构影响也对 hGST M2-2 对氨基色素、氰基 DMNG 和 DCNB 的特征性活性有贡献。