定制
计算机科学
合理设计
人工智能
蛋白质设计
生成语法
合成生物学
生成设计
蛋白质工程
图形
计算生物学
模块化设计
计算模型
生化工程
底物特异性
代谢工程
定向进化
序列(生物学)
工程类
生成模型
人工神经网络
蛋白质结构
可扩展性
渲染(计算机图形)
机器学习
计算机辅助设计
生物
作者
Hongling Shi,Xueyang Bai,Fangyuan Tian,Yangwan Li,Dandan Li,Lunguang Yao,Chuang Xue,Cunduo Tang
标识
DOI:10.1021/acs.jafc.6c01781
摘要
The rapid maturation of artificial intelligence (AI) has catalyzed a fundamental transition in biocatalysis, moving from structural analysis toward the prescriptive design of bespoke enzymes. This review synthesizes this AI-driven revolution, evaluating breakthroughs like AlphaFold2 and CLEAN that now bridge sequences with catalytic properties, including kinetic parameters and substrate specificity. We critically compare rational design strategies, contrasting evolutionary-guided redesign with the emerging generative de novo paradigm, where diffusion models and protein language models (PLMs) explore uncharacterized sequence space. By dissecting algorithms such as Graph Neural Networks and Transformers, we illustrate their role in deciphering protein chemistry's linguistic "grammar". Grounded in industrial cases, we demonstrate how AI overcomes bottlenecks like the stability-activity trade-off. Finally, we delineate the trajectory toward autonomous biofoundries and virtual cell modeling, envisioning engineered biocatalysts systematically integrated into complex metabolic networks─providing a roadmap for next-generation computational enzymology.
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