序列(生物学)
胺气处理
转氨酶
功能(生物学)
突变
化学
催化作用
生物
计算生物学
遗传学
生物化学
立体化学
酶
基因
有机化学
作者
Katrin Weigmann,Stephan Heijl,Bas Vroling,Nathalie Michels,Marian J. Menke,Mark Doerr,Lukas Schulig,Henk‐Jan Joosten,Uwe T. Bornscheuer
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-08-17
卷期号:: 15121-15131
标识
DOI:10.1021/acscatal.5c04248
摘要
Transaminases are essential biocatalysts for asymmetric synthesis in the pharmaceutical and fine chemical industries. Here, we report the application of 3DM Engineering─an AI-driven protein engineering platform─to optimize transaminase function by systematically exploring sequence-activity landscapes beyond those represented in the training data set. Our approach integrated the identification of hotspots from substrate tunnel analysis, enabling the construction of a focused, high-quality variant library targeting 53 residues for mutagenesis, which were subsequently used to train a protein language model. Further exploration of the sequence space identified mutations with previously unknown functional utility as salient targets for combination. The resulting higher-order variants displayed up to 21-fold improvement in catalytic efficiency and superior performance in the stereoselective synthesis of (S)-1-(2-chlorophenyl)ethanamine, achieving complete conversion and high enantiomeric excess (>99% ee). These results highlight the power of combining systematic hotspot identification with AI-driven exploration to discover unseen enzyme variants.
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