Gopich Irina V
Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, United States.
J Phys Chem B. 2021 Mar 4;125(8):2061-2073. doi: 10.1021/acs.jpcb.0c11155. Epub 2021 Feb 17.
Enzymatic cascade reactions, where a substrate is converted into a product in several steps, play a critical role in many biological systems. The enzymes in such reactions are often clustered inside intracellular compartments. To understand the effect of localization, we develop a theory for cascade reactions converting substrates into intermediates and then into products when the enzymes are localized in clusters. The theory shows that the kinetic scheme that describes the reaction with dispersed enzymes changes as a result of clustering. A new reaction channel, in which the substrate is directly converted into product, appears with a diffusion-influenced rate that is expressed in terms of enzyme catalytic efficiencies, diffusion coefficient, and cluster size. This rate is proportional to the cluster channeling probability, which is the probability that an intermediate is converted into product within the cluster in which the intermediate was formed. Simple analytic formulas allow one to quantify how enzyme clustering can affect product formation and regulate the direction of metabolic reaction flux in biological and synthetic systems. The rate of the substrate conversion decreases whereas the cluster channeling probability increases as the number of enzyme molecules in a cluster increases. The interplay between these factors leads to an optimal number of enzyme molecules that maximizes the clustering efficiency.
酶促级联反应在多个步骤中将底物转化为产物,在许多生物系统中起着关键作用。此类反应中的酶通常聚集在细胞内区室中。为了理解定位的影响,我们构建了一种理论,用于研究当酶聚集时将底物转化为中间体然后再转化为产物的级联反应。该理论表明,描述分散酶反应的动力学方案会因聚集而改变。一个新的反应通道出现了,其中底物直接转化为产物,其速率受扩散影响,该速率根据酶催化效率、扩散系数和聚集体大小来表示。这个速率与聚集体通道化概率成正比,聚集体通道化概率是指中间体在其形成的聚集体内转化为产物的概率。简单的解析公式使人们能够量化酶聚集如何影响产物形成以及调节生物和合成系统中代谢反应通量的方向。随着聚集体中酶分子数量的增加,底物转化速率降低,而聚集体通道化概率增加。这些因素之间的相互作用导致了一个最佳的酶分子数量,使聚集效率最大化。