Broo Kerstin, Larsson Anna-Karin, Jemth Per, Mannervik Bengt
Department of Biochemistry, Uppsala University, Biomedical Center, Box 576, SE-751 23 Uppsala, Sweden.
J Mol Biol. 2002 Apr 19;318(1):59-70. doi: 10.1016/S0022-2836(02)00032-3.
The correlation between sequence diversity and enzymatic function was studied in a library of Theta class glutathione transferases (GSTs) obtained by stochastic recombination of fragments of cDNA encoding human GST T1-1 and rat GST T2-2. In all, 94 randomly picked clones were characterized with respect to sequence, expression level, and catalytic activity in the conjugation reactions between glutathione and six alternative electrophilic substrates. Out of these six different compounds, dichloromethane is a selective substrate for human GST T1-1, whereas 1-menaphthyl sulfate and 1-chloro-2,4-dinitrobenzene are substrates for rat GST T2-2. The other three substances serve as substrates for both enzymes. Through this broad characterization, we have identified enzyme variants that have acquired novel activity profiles that differ substantially from those of the original GSTs. In addition, the expression levels of many clones were improved in comparison to the parental enzyme. A library of mutants can thus display a distribution of properties from which highly divergent evolutionary pathways may emerge, resembling natural evolutionary processes. From the GST library, a clone was identified that, by the point mutation N49D in the rat GST T2-2 sequence, has a 1700% increased activity with 1-menaphthyl sulfate and a 60% decreased activity with 4-nitrophenethyl bromide. Through the N49D mutation, the ratio of these activities has thus been altered 40-fold. An extensive characterization of a population of stochastically mutated enzymes can accordingly be used to find variants with novel substrate-activity profiles and altered catalytic properties. Recursive recombination of selected sequences displaying optimized properties is a strategy for the engineering of proteins for medical and biochemical applications. Such sequential design is combinatorial protein chemistry based on remodeling of existing structural scaffolds and has similarities to evolutionary processes in nature.
通过对编码人谷胱甘肽转移酶T1-1和大鼠谷胱甘肽转移酶T2-2的cDNA片段进行随机重组,构建了一个θ类谷胱甘肽转移酶(GSTs)文库,研究了序列多样性与酶功能之间的相关性。总共对94个随机挑选的克隆进行了序列、表达水平以及谷胱甘肽与六种替代亲电底物之间共轭反应中的催化活性的表征。在这六种不同的化合物中,二氯甲烷是人谷胱甘肽转移酶T1-1的选择性底物,而1-萘基硫酸酯和1-氯-2,4-二硝基苯是大鼠谷胱甘肽转移酶T2-2的底物。其他三种物质是这两种酶的底物。通过这种广泛的表征,我们鉴定出了具有与原始GSTs显著不同的新活性谱的酶变体。此外,与亲本酶相比,许多克隆的表达水平有所提高。因此,一个突变体文库可以展示出一系列特性分布,从中可能出现高度不同的进化途径,类似于自然进化过程。从GST文库中鉴定出一个克隆,通过大鼠谷胱甘肽转移酶T2-2序列中的点突变N49D,其对1-萘基硫酸酯的活性增加了1700%,而对4-硝基苯乙基溴的活性降低了60%。通过N49D突变,这些活性的比例因此改变了40倍。因此,对一组随机突变酶的广泛表征可用于寻找具有新底物活性谱和改变的催化特性的变体。对显示出优化特性的选定序列进行递归重组是一种用于医学和生化应用的蛋白质工程策略。这种顺序设计是基于对现有结构支架进行重塑的组合蛋白质化学,与自然界中的进化过程有相似之处。