Data-efficient protein mutational effect prediction with weak supervision by molecular simulation and protein language models
Open accessPublished version of a preprint
Abstract
Machine learning-based protein mutational effect prediction is widely used in protein engineering and pathogenicity prediction, but training data scarcity remains a major challenge due to high costs of experimental measurements. A previous study proposed data augmentation using computational estimates by molecular simulation. However, this approach has been limited to predicting mutational effects on thermostability. Here, we present a new data augmentation method that combines molecular simulation with zero-shot prediction computed by protein language models. These computational estimates serve as ‘weak’ training data to supplement experimental training data. Our method dynamically adjusts the weight and inclusion of weak training data based on available experimental training data. This reduces potential negative impacts of weak training data while extending applicability to diverse protein properties such as binding affinity and enzymatic activity. Benchmark tests demonstrate that our method improves prediction accuracy particularly when experimental training data are scarce. These results indicate the capability of our approach to advance protein engineering and pathogenicity prediction in small data regimes.
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Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764 · see citing works
Evolutionary-scale prediction of atomic level protein structure with a language model
Lin, Z., Akin, H., Rao, R., Hie, B., Zhu, Z., Lu, W., Smetanin, N., Verkuil, R., Kabeli, O., Shmueli, Y., et al. (2022) · doi:10.1101/2022.07.20.500902 · Cited by 5,523 · see citing works
An end-to-end framework for the prediction of protein structure and fitness from single sequence
Chen, Y., Xu, Y., Liu, D., Xing, Y., & Gong, H. (2024) · Nature Communications · doi:10.1038/s41467-024-51776-x · Cited by 45 · see citing works
Xu, Y., Liu, D., & Gong, H. (2024) · Nature Computational Science · doi:10.1038/s43588-024-00716-2 · Cited by 41 · see citing works
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- Authors
- Deguchi, T., Ab Ghani, N. S., Kurumida, Y., Iida, S., Kobayashi, K., & Saito, Y.
- Affiliations
- Artificial Intelligence Research Center (JP)
- School of Frontier Engineering, Kitasato University , 1-15-1 Kitazato, Minami-ku, Sagamihara, Kanagawa 252-0373 ,
- Kitasato University (JP)
- Graduate School of Frontier Sciences, The University of Tokyo , 5-1-5, Kashiwanoha, Kashiwa, Chiba 277-0882 ,
- Venue
- Briefings in Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2025-08-31
- Volume
- 26
- Issue
- 5
- ISSN
- 1467-5463 (ISSN-L)
- 1477-4054
- PMC
- PMC12513171
- OpenAlex
- W4415046037
- Cited by
- 2
- References
- 4
- Citations by year
- 2026: 2
- FWCI
- 0.60
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Briefings in Bioinformatics (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- JSPS (22H03691)
- AMED (JP19ak0101122)
- NEDO (JPNP14004)
- JACI Prize for Encouraging Young Researcher
- JST SPRING (JPMJSP2108)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- weakly supervised learning, data augmentation, molecular simulation, protein language models, zero-shot prediction, data scarcity, protein thermal stability, binding affinity prediction, pathogenicity prediction, protein engineering
- MeSH terms
- Machine Learning, Mutation, Proteins, Computational Biology, Molecular Dynamics Simulation
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