College of Biotechnology, Tianjin University of Science & Technology, Tianjin, China.
Key Laboratory of Industrial Fermentation Microbiology, Ministry of Education, Tianjin Key Laboratory of Industrial Microbiology, Tianjin, China.
Protein Sci. 2023 Dec;32(12):e4837. doi: 10.1002/pro.4837.
Psychrophilic proteases have attracted enormous attention in past decades, due to their high catalytic activity at low temperatures in a wide range of industrial processes, especially in the detergent and leather industries. Among them, H5 is an alkaline protease mutant, which featuring psychrophilic-like behavior, but the reasons that H5 with higher activity at low temperatures are still poorly understood. Herein, the molecular dynamics (MD) simulations combined with residue interaction network (RIN) were utilized to investigate the mechanisms of the cold-adaption of mutant H5. The results demonstrated that two loops involved in the substrate binding G100-S104 and S125-S129 in H5 had higher mobility, and the distance enlargement between the two loops modulated the substrate's accessibility compared with wild type counterpart. Besides, H5 enhanced conformational flexibility by weakening salt bridges and increasing interaction with the solvent. In particular, the absence of Lys251-Asp197-Arg247 salt bridge network may contribute to the structural mobility. Based on the free energy landscape and molecular mechanics Poisson-Boltzmann surface area of the wild type and H5, it was elucidated that H5 possessed a large population of interconvertible conformations, resulting in the weaker substrate binding free energy. The calculated RIN topology parameters such as the average degree, average cluster coefficient, and average path length further verified that the mutant H5 attenuated residue-to-residue interactions. The investigation of the mechanisms by which how the residue mutation affects the stability and activity of enzymes provides a theoretical basis for the development of cold-adapted protease.
在过去的几十年中,嗜冷蛋白酶因其在广泛的工业过程中(尤其是在洗涤剂和制革工业中)在低温下具有高催化活性而引起了极大的关注。其中,H5 是一种碱性蛋白酶突变体,具有嗜冷样行为,但 H5 在低温下具有更高活性的原因仍知之甚少。在此,利用分子动力学(MD)模拟结合残基相互作用网络(RIN)研究了突变体 H5 适应低温的机制。结果表明,涉及底物结合 G100-S104 和 S125-S129 的两个环的运动性更高,并且与野生型相比,两个环之间的距离扩大调制了底物的可及性。此外,H5 通过削弱盐桥并增加与溶剂的相互作用来增强构象灵活性。特别是,Lys251-Asp197-Arg247 盐桥网络的缺失可能有助于结构的流动性。基于野生型和 H5 的自由能景观和分子力学泊松-玻尔兹曼表面面积,阐明了 H5 具有大量可相互转化的构象,从而导致较弱的底物结合自由能。计算得出的 RIN 拓扑参数(例如平均度数、平均簇系数和平均路径长度)进一步证明了突变体 H5 减弱了残基间的相互作用。研究残基突变如何影响酶的稳定性和活性的机制为开发适应低温的蛋白酶提供了理论基础。