Department of Biochemistry, Stanford University , Stanford, California 94305, United States.
Biochemistry. 2013 Dec 23;52(51):9167-76. doi: 10.1021/bi4010045. Epub 2013 Dec 11.
Catalytic promiscuity, an evolutionary concept, also provides a powerful tool for gaining mechanistic insights into enzymatic reactions. Members of the alkaline phosphatase (AP) superfamily are highly amenable to such investigation, with several members having been shown to exhibit promiscuous activity for the cognate reactions of other superfamily members. Previous work has shown that nucleotide pyrophosphatase/phosphodiesterase (NPP) exhibits a >10⁶-fold preference for the hydrolysis of phosphate diesters over phosphate monoesters, and that the reaction specificity is reduced 10³-fold when the size of the substituent on the transferred phosphoryl group of phosphate diester substrates is reduced to a methyl group. Here we show additional specificity contributions from the binding pocket for this substituent (herein termed the R' substituent) that account for an additional ~250-fold differential specificity with the minimal methyl substituent. Removal of four hydrophobic side chains suggested on the basis of structural inspection to interact favorably with R' substituents decreases phosphate diester reactivity 10⁴-fold with an optimal diester substrate (R' = 5'-deoxythymidine) and 50-fold with a minimal diester substrate (R' = CH₃). These mutations also enhance the enzyme's promiscuous phosphate monoesterase activity by nearly an order of magnitude, an effect that is traced by mutation to the reduction of unfavorable interactions with the two residues closest to the nonbridging phosphoryl oxygen atoms. The quadruple R' pocket mutant exhibits the same activity toward phosphate diester and phosphate monoester substrates that have identical leaving groups, with substantial rate enhancements of ~10¹¹-fold. This observation suggests that the Zn²⁺ bimetallo core of AP superfamily enzymes, which is equipotent in phosphate monoester and diester catalysis, has the potential to become specialized for the hydrolysis of each class of phosphate esters via addition of side chains that interact with the substrate atoms and substituents that project away from the Zn²⁺ bimetallo core.
催化的多功能性是一个进化概念,它也为深入了解酶反应的机制提供了一个强大的工具。碱性磷酸酶(AP)超家族的成员非常适合进行这种研究,已经有几个成员被证明具有对其他超家族成员的同工反应的多功能活性。以前的工作表明,核苷酸焦磷酸酶/磷酸二酯酶(NPP)对磷酸二酯的水解表现出超过 10⁶倍的偏好,而当磷酸二酯底物上转移的磷酸基的取代基的大小减小到甲基时,反应特异性降低 10³倍。在这里,我们展示了结合口袋对这个取代基(在此称为 R'取代基)的额外特异性贡献,这使得与最小甲基取代基相比,额外的 ~250 倍的差异特异性。根据结构检查,有四个疏水性侧链被认为有利于与 R'取代基相互作用,这些侧链的去除使磷酸二酯的反应性降低了 10⁴倍,对于最佳二酯底物(R'=5'-脱氧胸苷)和 50 倍,对于最小的二酯底物(R'=CH₃)。这些突变还使酶的多功能磷酸单酯酶活性提高了近一个数量级,这种效应可以通过突变追踪到与最接近非桥接磷酸氧原子的两个残基的不利相互作用的减少。四联体 R'口袋突变体对具有相同离去基团的磷酸二酯和磷酸单酯底物表现出相同的活性,具有约 10¹¹倍的显著速率增强。这一观察结果表明,AP 超家族酶的 Zn²⁺双金属核心在磷酸单酯和二酯催化中具有同等的效力,通过添加与底物原子相互作用的侧链,有可能专门用于水解每一类磷酸酯,这些侧链与从 Zn²⁺双金属核心伸出的取代基相互作用。