ArticleScientific reports2025
Predicting drug-target interactions using machine learning with improved data balancing and feature engineering.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- EPIC: A Machine-Learning Framework for Product-Dependent Behavior in β‑Glucosidases.ACS omega · 2026Article
- Artificial Intelligence Across the Drug Development Lifecycle.Medical sciences (Basel, Switzerland) · 2026Review
- Predicting drug-target interactions and binding affinity using an optimized deep learning approach.Journal of computer-aided molecular design · 2026Article
- TriDTI: tri-modal representation learning with cross-modal alignment for drug-target interaction prediction.Briefings in bioinformatics · 2026Article
- Machine Learning for Multi-Target Drug Discovery: Challenges and Opportunities in Systems Pharmacology.Pharmaceutics · 2025Review
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Drug-Target Interaction (DTI) prediction is a vital task in drug discovery, yet it faces significant challenges such as data imbalance and the complexity of biochemical representations. This study makes several contributions to address these issues, introducing a novel hybrid framework that combines advanced machine learning (ML) and deep learning (DL) techniques. The framework leverages comprehensive feature engineering, utilizing MACCS keys to extract structural drug features and amino acid/dipeptide compositions to represent target biomolecular properties. This dual feature extraction method enables a deeper understanding of chemical and biological interactions, enhancing predictive accuracy. To address data imbalance, Generative Adversarial Networks (GANs) are employed to create synthetic data for the minority class, effectively reducing false negatives and improving the sensitivity of the predictive model. The Random Forest Classifier (RFC) is utilized to make precise DTI predictions, optimized for handling high-dimensional data. The proposed framework's scalability and robustness were validated across diverse datasets, including BindingDB-Kd, BindingDB-Ki, and BindingDB-IC50. For the BindingDB-Kd dataset, the GAN+RFC model achieved remarkable performance metrics: accuracy of 97.46%, precision of 97.49%, sensitivity of 97.46%, specificity of 98.82%, F1-score of 97.46%, and ROC-AUC of 99.42%. Similarly, for the BindingDB-Ki dataset, the model attained an accuracy of 91.69%, precision of 91.74%, sensitivity of 91.69%, specificity of 93.40%, F1-score of 91.69%, and ROC-AUC of 97.32%. On the BindingDB-IC50 dataset, the model achieved an accuracy of 95.40%, precision of 95.41%, sensitivity of 95.40%, specificity of 96.42%, F1-score of 95.39%, and ROC-AUC of 98.97%. These results demonstrate the efficacy of the GAN-based approach in capturing complex patterns, significantly improving DTI prediction outcomes. In conclusion, the proposed GAN-based hybrid framework sets a new benchmark in computational drug discovery by addressing critical challenges in DTI prediction. Its robust performance, scalability, and generalizability contribute substantially to therapeutic development and pharmaceutical research.
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