定向进化
定向分子进化
酶
合理设计
计算生物学
支架蛋白
嵌入
合成生物学
催化作用
纳米技术
蛋白质工程
生物
化学
计算机科学
蛋白质设计
生化工程
蛋白质结构
工程类
生物化学
材料科学
信号转导
人工智能
基因
突变体
作者
H. Adrian Bunzel,J. L. Ross Anderson,Adrian J. Mulholland
标识
DOI:10.1016/j.sbi.2020.12.015
摘要
De novo enzymes can be created by computational design and directed evolution. Here, we review recent insights into the origins of catalytic power in evolved designer enzymes to pinpoint opportunities for next-generation designs: Evolution precisely organizes active sites, introduces catalytic H-bonding networks, invokes electrostatic catalysis, and creates dynamical networks embedding the active site in a reactive protein scaffold. Such insights foster our fundamental knowledge of enzyme catalysis and fuel the future design of tailor-made enzymes.
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