SFM-Net: Selective Fusion of Multiway Protein Feature Network for Predicting Binding Affinity Changes upon Mutations
Accurately predicting the effect of mutations on protein-protein interactions (PPIs) is essential for understanding the protein structure and function, as well as providing insights into disease-causing mechanisms. Many recent popular approaches based on the three-dimensional structure of proteins have been proposed to predict the changes in binding affinity caused by mutations, i.e. ΔΔ<i>G</i>. However, how to effectively use the structural information to comprehensively exploit complex interactions within proteins and integrate multisource features remains a significant challenge. In this study, we propose SFM-Net, a powerful deep learning model constructed with GNN-based multiway feature extractors and a new context-aware selective fusion module that jointly leverages the sequence, structural, and evolutionary information. Such design enables SFM-Net to effectively and selectively use features from different sources to facilitate binding affinity change prediction. Benchmarking experiments and targeted ablation studies illustrate the effectiveness and robustness of our method for improving the binding affinity change prediction.
Authors
- Hiroyuki Ogata (ORCID: https://orcid.org/0000-0001-6594-377X)
- Jiangning Song (ORCID: https://orcid.org/0000-0001-8031-9086)
- Tatsuya Akutsu (ORCID: https://orcid.org/0000-0001-9763-797X)
- C. Karen Liu (ORCID: https://orcid.org/0009-0000-9829-6695)
- Sudong Cai (ORCID: https://orcid.org/0000-0002-5446-5618)
- Tong Pan (ORCID: https://orcid.org/0009-0002-5857-2768)
Institutions
- Kyoto University (JP)
- Discovery Institute (US)
- Australian Regenerative Medicine Institute (AU)
- Instituto de Investigaciones Químicas (ES)
- Avenir Health (US)
- Monash University (AU)
Publication Details
- Journal
- Journal of Chemical Information and Modeling
- Published
- 2025-03-20
- DOI
- https://doi.org/10.1021/acs.jcim.5c00130
- Citations
- 2
- Primary Topic
- Protein Structure and Dynamics
- Type
- article
- Field-Weighted Citation Impact
- 1.61
Funders
- Monash University
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency
- Institute for Chemical Research, Kyoto University