Department of Chemistry & Chemical Biology, Northeastern University, Boston, MA, United States of America.
Department of Physics, Northeastern University, Boston, MA, United States of America.
PLoS One. 2020 Feb 6;15(2):e0228487. doi: 10.1371/journal.pone.0228487. eCollection 2020.
Understanding how enzymes achieve their tremendous catalytic power is a major question in biochemistry. Greater understanding is also needed for enzyme engineering applications. In many cases, enzyme efficiency and specificity depend on residues not in direct contact with the substrate, termed remote residues. This work focuses on Escherichia coli ornithine transcarbamoylase (OTC), which plays a central role in amino acid metabolism. OTC has been reported to undergo an induced-fit conformational change upon binding its first substrate, carbamoyl phosphate (CP), and several residues important for activity have been identified. Using computational methods based on the computed chemical properties from theoretical titration curves, sequence-based scores derived from evolutionary history, and protein surface topology, residues important for catalytic activity were predicted. The roles of these residues in OTC activity were tested by constructing mutations at predicted positions, followed by steady-state kinetics assays and substrate binding studies with the variants. First-layer mutations R57A and D231A, second-layer mutation H272L, and third-layer mutation E299Q, result in 57- to 450-fold reductions in kcat/KM with respect to CP and 44- to 580-fold reductions with respect to ornithine. Second-layer mutations D140N and Y160S also reduce activity with respect to ornithine. Most variants had decreased stability relative to wild-type OTC, with variants H272L, H272N, and E299Q having the greatest decreases. Variants H272L, E299Q, and R57A also show compromised CP binding. In addition to direct effects on catalytic activity, effects on overall protein stability and substrate binding were observed that reveal the intricacies of how these residues contribute to catalysis.
了解酶如何实现其巨大的催化能力是生物化学中的一个主要问题。酶工程应用也需要更深入的了解。在许多情况下,酶的效率和特异性取决于与底物没有直接接触的残基,称为远程残基。这项工作集中在大肠杆菌鸟氨酸转氨甲酰酶(OTC)上,它在氨基酸代谢中起着核心作用。据报道,OTC 在结合其第一个底物氨甲酰磷酸(CP)时会经历一个诱导契合构象变化,并且已经确定了几个对活性很重要的残基。使用基于理论滴定曲线计算出的化学性质、基于进化历史的序列得分和蛋白质表面拓扑学的计算方法,预测了对催化活性很重要的残基。通过在预测位置构建突变,然后进行稳态动力学测定和变体的底物结合研究,测试了这些残基在 OTC 活性中的作用。第一层突变 R57A 和 D231A、第二层突变 H272L 和第三层突变 E299Q,导致 kcat/KM 相对于 CP 降低了 57-450 倍,相对于鸟氨酸降低了 44-580 倍。第二层突变 D140N 和 Y160S 也降低了鸟氨酸的活性。与野生型 OTC 相比,大多数变体的稳定性降低,其中 H272L、H272N 和 E299Q 的降低幅度最大。变体 H272L、E299Q 和 R57A 也显示出 CP 结合能力受损。除了对催化活性的直接影响外,还观察到对整体蛋白质稳定性和底物结合的影响,这揭示了这些残基如何参与催化的复杂性。