Department of Chemistry, Colorado School of Mines, 1500 Illinois Street, Golden, Colorado 80401, United States.
Department of Chemistry, and Biochemistry, University of California, Los Angeles, 607 Charles E. Young Drive East, Los Angeles, California 90095, United States.
J Chem Theory Comput. 2023 Feb 14;19(3):694-704. doi: 10.1021/acs.jctc.2c01060. Epub 2022 Dec 23.
Enzymes host active sites inside protein macromolecules, which have diverse, often incredibly complex, and atom-expensive structures. It is an outstanding question what the role of these expensive scaffolds might be in enzymatic catalysis. Answering this question is essential to both enzymology and the design of artificial enzymes with proficiencies that will match those of the best natural enzymes. Protein rigidifying the active site, contrasted with the dynamics and vibrational motion promoting the reaction, as well as long-range electrostatics (also known as electrostatic preorganization) were all proposed as central contributions of the scaffold to the catalysis. Here, we show that all these effects inevitably produce changes in the quantum mechanical electron density in the active site, which in turn defines the reactivity. The phenomena are therefore fundamentally inseparable. The geometry of the electron density-a scalar field characterized by a number of mathematical features such as critical points-is a rigorous and convenient descriptor of enzymatic catalysis and a reporter on the role of the protein. We show how this geometry can be analyzed, linked to the reaction barriers, and report in particular on intramolecular electric fields in enzymes. We illustrate these tools on the studies of electrostatic preorganization in several representative enzyme classes, both natural and artificial. We highlight the forward-looking aspects of the approach.
酶在蛋白质大分子中承载活性部位,这些部位具有多种多样、通常令人难以置信的复杂、原子昂贵的结构。这些昂贵支架在酶催化中的作用是什么,这是一个悬而未决的问题。回答这个问题对于酶学和设计具有与最佳天然酶相匹配的专业知识的人工酶都至关重要。蛋白质刚性化活性部位,与促进反应的动力学和振动运动形成对比,以及远程静电(也称为静电预组织)都被提议作为支架对催化的核心贡献。在这里,我们表明,所有这些效应不可避免地会在活性部位中产生量子力学电子密度的变化,而电子密度反过来又定义了反应性。因此,这些现象从根本上是不可分割的。电子密度的几何形状——由一些数学特征(如临界点)描述的标量场——是酶催化的严格而方便的描述符,也是蛋白质作用的报告。我们展示了如何分析这种几何形状,将其与反应势垒联系起来,并特别报告酶中的分子内电场。我们在几个代表性的天然和人工酶类中对静电预组织的研究中说明了这些工具。我们强调了该方法的前瞻性方面。