Accelerated enzyme engineering by machine-learning guided cell-free expression

Grant M. Landwehr, Jonathan W. Bogart, Carol Magalhaes, Eric Hammarlund, Ashty S. Karim, Michael C. Jewett

Nature Communications 2025 article cited by 134

importance 5/10 solved Enzyme Catalysis and Immobilization enzyme engineering stage: research

Engineering enzymes is slow because generating large sequence-function datasets for predictive design is difficult.

Faster enzyme engineering enables cheaper biological production of pharmaceuticals and chemicals.

An ML-guided platform integrating cell-free DNA assembly, cell-free expression, and functional assays mapped fitness landscapes; augmented ridge regression models predicted amide synthetase variants for pharmaceutical synthesis.

1,217 enzyme variants evaluated in 10,953 unique reactions; models predicted variants for 9 small molecule pharmaceuticals

Demonstrated ML-guided engineering of amide synthetases across multiple reactions in a peer-reviewed venue.

Venue Nature Communications
Published 2025
Work type article
Authors Grant M. Landwehr, Jonathan W. Bogart, Carol Magalhaes, Eric Hammarlund, Ashty S. Karim, Michael C. Jewett
Citations 134 (OpenAlex, at import time)
References 75
Model or method augmented ridge regression
Organization not stated in source
Primary source https://doi.org/10.1038/s41467-024-55399-0
Open access gold
Keywords machine learning, enzyme engineering, cell-free expression, amide synthetase, biocatalysis
5 / 10

real but narrower advance

ML-guided enzyme engineering accelerates biocatalyst design for pharmaceutical synthesis; real advance but demonstrated on specific amide synthetase reactions.

Basis: inferred. Judged from the source text, which gives no explicit scale. Stated scale: not stated in source. Method and limits.

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