ArticleProtein science : a publication of the Protein Society2024
A protein fitness predictive framework based on feature combination and intelligent searching.
Article in Protein science : a publication of the Protein Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Biosynthesis and Microbial Production of Carminic Acid: From Pathway Elucidation to Synthetic Biology.Microorganisms · 2026Review
- Intrinsic dataset features drive mutational effect prediction by protein language models.bioRxiv : the preprint server for biology · 2026Article
- A comprehensive review of histone modifications during mammalian oogenesis and early embryo development.Histochemistry and cell biology · 2025Review
- A protein fitness predictive framework based on feature combination and intelligent searching.Protein science : a publication of the Protein Society · 2024Article
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Authors and funding
8 authors.
Funding
Abstract
Machine learning (ML) constructs predictive models by understanding the relationship between protein sequences and their functions, enabling efficient identification of protein sequences with high fitness values without falling into local optima, like directional evolution. However, how to extract the most pertinent functional feature information from a limited number of protein sequences is vital for optimizing the performance of ML models. Here, we propose scut_ProFP (Protein Fitness Predictor), a predictive framework that integrates feature combination and feature selection techniques. Feature combination offers comprehensive sequence information, while feature selection searches for the most beneficial features to enhance model performance, enabling accurate sequence-to-function mapping. Compared to similar frameworks, scut_ProFP demonstrates superior performance and is also competitive with more complex deep learning models-ECNet, EVmutation, and UniRep. In addition, scut_ProFP enables generalization from low-order mutants to high-order mutants. Finally, we utilized scut_ProFP to simulate the engineering of the fluorescent protein CreiLOV and highly enriched mutants with high fluorescence based on only a small number of low-fluorescence mutants. Essentially, the developed method is advantageous for ML in protein engineering, providing an effective approach to data-driven protein engineering. The code and datasets for scut_ProFP are available at https://github.com/Zhang66-star/scut_ProFP.
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Registered trials
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