Liu Yuanchao, Hickey David P, Minteer Shelley D, Dickson Alex, Calabrese Barton Scott
Department of Chemical Engineering and Materials Science and Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824, United States.
Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
J Phys Chem C Nanomater Interfaces. 2019 Jun 20;123(24):15284-15292. doi: 10.1021/acs.jpcc.9b02844. Epub 2019 May 22.
Electrostatic channeling is a naturally occurring approach to control the flux of charged intermediates in catalytic cascades. Computational techniques have enabled quantitative understanding of such mechanisms, augmenting experimental approaches by modeling molecular interactions in atomic detail. In this work, we report the first utilization of a Markov-state model (MSM) to describe the surface diffusion of a reaction intermediate, glucose 6-phosphate, on an artificially modified cascade where hexokinase and glucose-6-phosphate dehydrogenase are covalently conjugated by a cationic oligopeptide bridge. Conformation space networks are used to represent intermediate transport on enzyme surfaces, along with committor probabilities that assess the desorption probability of the intermediate on each segment of the channeling pathway. For the region between the peptide bridge and downstream active site, the ionic strength dependence of desorption probability by MSM agreed well with that by transition state theory. A kinetic Monte Carlo model integrates parameters from different computational methods to evaluate the contribution of desorption during each step. The approach is validated by calculation of kinetic lag time, which agrees well with experimental results. These results further demonstrate the applicability of molecular simulations and advanced sampling techniques to the design of chemical networks.
静电通道效应是一种自然存在的控制催化级联反应中带电中间体通量的方法。计算技术使得人们能够对这类机制进行定量理解,通过对分子相互作用进行原子尺度的建模来补充实验方法。在这项工作中,我们首次利用马尔可夫状态模型(MSM)来描述反应中间体6-磷酸葡萄糖在人工修饰的级联反应中的表面扩散,在该反应中己糖激酶和6-磷酸葡萄糖脱氢酶通过阳离子寡肽桥共价连接。构象空间网络用于表示酶表面的中间体转运,同时用反应坐标概率来评估中间体在通道化途径各段上的解吸概率。对于肽桥和下游活性位点之间的区域,MSM计算得到的解吸概率对离子强度的依赖性与过渡态理论计算结果吻合良好。动力学蒙特卡罗模型整合了来自不同计算方法的参数,以评估每一步中解吸的贡献。通过计算动力学滞后时间对该方法进行了验证,计算结果与实验结果吻合良好。这些结果进一步证明了分子模拟和先进采样技术在化学网络设计中的适用性。