- Title
- Distance plus attention for binding affinity prediction
- Creator
- Rahman, Julia; Newton, M. A. Hakim; Ali, Mohammed Eunus; Sattar, Abdul
- Relation
- Journal of Cheminformatics Vol. 16, no. 52
- Publisher Link
- http://dx.doi.org/10.1186/s13321-024-00844-x
- Publisher
- BioMed Central (BMC)
- Resource Type
- journal article
- Date
- 2024
- Description
- Protein-ligand binding affinity plays a pivotal role in drug development, particularly in identifying potential ligands for target disease-related proteins. Accurate affinity predictions can significantly reduce both the time and cost involved in drug development. However, highly precise affinity prediction remains a research challenge. A key to improve affinity prediction is to capture interactions between proteins and ligands effectively. Existing deep-learning-based computational approaches use 3D grids, 4D tensors, molecular graphs, or proximity-based adjacency matrices, which are either resource-intensive or do not directly represent potential interactions. In this paper, we propose atomic-level distance features and attention mechanisms to capture better specific protein-ligand interactions based on donor-acceptor relations, hydrophobicity, and π-stacking atoms. We argue that distances encompass both short-range direct and long-range indirect interaction effects while attention mechanisms capture levels of interaction effects. On the very well-known CASF-2016 dataset, our proposed method, named Distance plus Attention for Affinity Prediction (DAAP), significantly outperforms existing methods by achieving Correlation Coefficient (R) 0.909, Root Mean Squared Error (RMSE) 0.987, Mean Absolute Error (MAE) 0.745, Standard Deviation (SD) 0.988, and Concordance Index (CI) 0.876. The proposed method also shows substantial improvement, around 2% to 37%, on five other benchmark datasets. The program and data are publicly available on the website https://gitlab.com/mahnewton/daap. Scientific Contribution Statement This study innovatively introducesdistance-based features to predict protein-ligand binding affinity, capitalizing onunique molecular interactions. Furthermore, the incorporation of protein sequencefeatures of specific residues enhances the model’s proficiency in capturing intricatebinding patterns. The predictive capabilities are further strengthened through theuse of a deep learning architecture with attention mechanisms, and an ensembleapproach, averaging the outputs of five models, is implemented to ensure robustand reliable predictions.
- Subject
- binding affinity; distance matrix; donor-acceptor; hydrophobicity; π-Stacking; deep learning
- Identifier
- http://hdl.handle.net/1959.13/1504496
- Identifier
- uon:55538
- Identifier
- ISSN:1758-2946
- Rights
- x
- Language
- eng
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