Integrating protein language models and automatic biofoundry for enhanced protein evolution.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39934638.
- Also identified by DOI 10.1038/s41467-025-56751-8 and PMC identifier 11814318.
- Licence recorded as CC BY-NC-ND.
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Abstract
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.
Medical subject headings
- Directed Molecular Evolution
- Protein Engineering
- Proteins