化学
活动站点
定向进化
催化作用
合成生物学
酶
熵(时间箭头)
过渡状态
蛋白质工程
生化工程
纳米技术
组合化学
计算生物学
生物系统
蛋白质设计
蛋白质结构
生物化学
酶催化
热力学
有机化学
物理
材料科学
突变体
工程类
基因
生物
作者
Valerie Vaissier Welborn,Teresa Head‐Gordon
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2018-10-02
卷期号:119 (11): 6613-6630
被引量:174
标识
DOI:10.1021/acs.chemrev.8b00399
摘要
We review the standard model for de novo computational design of enzymes, which primarily focuses on the development of an active-site geometry, composed of protein functional groups in orientations optimized to stabilize the transition state, for a novel chemical reaction not found in nature. Its emphasis is placed on the structure and energetics of the active site embedded in an accommodating protein that serves as a physical support that shields the reaction chemistry from solvent, which is typically improved upon by laboratory-directed evolution. We also provide a review of design strategies that move beyond the standard model, by placing more emphasis on the designed enzyme as a whole catalytic construct. Starting with complete de novo enzyme design examples, we consider additional design factors such as entropy of individual residues, correlated motion between side chains (mutual information), dynamical correlations of the enzyme motions that could aid the reaction, reorganization energy, and electric fields as ways to exploit the entire protein scaffold to improve upon the catalytic rate, thereby providing directed evolution with better starting sequences for increasing biocatalytic performance.
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