定向进化
计算机科学
蛋白质工程
定向分子进化
人工智能
突变体
生物
酶
生物化学
基因
作者
Qiang Zhang,Wanyi Chen,Ming Qin,Yuhao Wang,Zhongji Pu,Keyan Ding,Yuyue Liu,Qunfeng Zhang,Dongfang Li,Xinjia Li,Yu Zhao,Jianhua Yao,Lei Huang,Jianping Wu,Lirong Yang,Huajun Chen,Haoran Yu
标识
DOI:10.1038/s41467-025-56751-8
摘要
Traditional protein engineering methods, such as directed evolution, while effective, are often slow and labor-intensive. Advances in machine learning and automated biofoundry present new opportunities for optimizing these processes. This study devises a protein language model-enabled automatic evolution platform, a closed-loop system for automated protein engineering within the Design-Build-Test-Learn cycle. The protein language model ESM-2 makes zero-shot prediction of 96 variants to initiate the cycle. The biofoundry constructs and evaluates these variants, and feeds the results back to a multi-layer perceptron to train a fitness predictor, which then makes prediction of second round of 96 variants with improved fitness. With the tRNA synthetase as a model enzyme, four-rounds of evolution carried out within 10 days lead to mutants with enzyme activity improved by up to 2.4-fold. Our system significantly enhances the speed and accuracy of protein evolution, driving faster advancements in protein engineering for industrial applications. Traditional protein engineering methods are often slow and labor-intensive. Here, authors develop an automatic protein evolution platform enabled by a protein language model. Using this platform, they significantly improved the activity of a tRNA synthetase within ten days.
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