Motivation:
The prediction of drug-target interaction (DTI) from heterogeneous biological data is critical to predict drugs and therapeutic targets for known diseases such as tumor and bowel disease. The study of DTI based on drug representation learning can strengthen or integrate our knowledge of pharmacological and chemical phenomena. Therefore, there is a strong motivation to develop effective methods that can detect these potential drug-target interactions.
Results:
We have developed a novel Knowledge-Enhanced Multi-View framework (KEMV) to predict unknown DTIs from pharmacological data and chemical data on a large scale. The proposed method consists of two steps: (i) learning more comprehensive drug representations via the proposed multi-view attention mechanism, which bridges pharmacological and chemical information, and interactively summarizes the attention values depending on varying interactions between different pairs of drug features. (ii) predicting unknown drug-target interactions based on the drug and target representations. The method is tested on real-world dataset KEGG with three classes of important drug–target interactions involving enzymes, ion channels, and G-protein-coupled receptors. Our framework is proven to uncover potential DTIs with scientific evidences explaining the mechanism of the interactions through the processing of high-dimensional, heterogeneous, and sparse drug data.
Availability:
The originality of the proposed method lies in the attentive integration of pharmacological and chemical information for representation of drug candidate compounds and the prediction of drug-target interaction toward drug discovery in a unified framework. Our results are reproducible and and code is available at:
https://github.com/YuanKQ/DTI-Prediction
.
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关键词
Medical data processing,neural networks,multi-view attention,drug-target interaction prediction
