Graph neural pre-training based drug-target affinity prediction
Computational drug-target affinity prediction has the potential to accelerate drug discovery. Currently, pre-training models have achieved significant success in various fields due to their ability to train the model using vast amounts of unlabeled data. However, given the scarcity of drug-target interaction data, pre-training models can only be trained separately on drug and target data, resulting in features that are insufficient for drug-target affinity prediction. To address this issue, in this paper, we design a graph neural pre-training-based drug-target affinity prediction method (GNPDTA). This approach comprises three stages. In the first stage, two pre-training models are utilized to extract low-level features from drug atom graphs and target residue graphs, leveraging a large number of unlabeled training samples. In the second stage, two 2D convolutional neural networks are employed to combine the extracted drug atom features and target residue features into high-level representations of drugs and targets. Finally, in the third stage, a predictor is used to predict the drug-target affinity. This approach fully utilizes both unlabeled and labeled training samples, enhancing the effectiveness of pre-training models for drug-target affinity prediction. In our experiments, GNPDTA outperforms other deep learning methods, validating the efficacy of our approach.
Authors
- Qing Ye (ORCID: https://orcid.org/0000-0003-3927-1919)
- Yaxin Sun
Institutions
- Zhejiang Normal University (CN)
- Wenzhou University (CN)
- Zhejiang Medicine (China) (CN)
- Wenzhou University of Technology
Publication Details
- Journal
- Frontiers in Genetics
- Published
- 2024-09-16
- DOI
- https://doi.org/10.3389/fgene.2024.1452339
- Citations
- 4
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 1.45
Funders
- National Natural Science Foundation of China