Abstract

Identification of drug-target interactions (DTIs) plays a crucial role in drug development. Traditional laboratory-based DTI discovery is generally costly and time-consuming. Therefore, computational approaches have been developed to predict interactions between drug candidates and disease-causing proteins. We designed a novel method, termed heterogeneous information integration for DTI prediction (HIDTI), based on the concept of predicting vectors for all of unknown/unavailable heterogeneous drug- and protein-related information. We applied a residual network in HIDTI to extract features of such heterogeneous information for predicting DTIs, and tested the model using drug-based ten-fold cross-validation to examine the prediction performance for unseen drugs. As a result, HIDTI outperformed existing models using heterogeneous information, and was demonstrating that our method predicted heterogeneous information on unseen data better than other models. In conclusion, our study suggests that HIDTI has the potential to advance the field of drug development by accurately predicting the targets of new drugs.

Highlights

  • We developed a new approach, termed heterogeneous information integration for drug-target interactions (DTIs) prediction (HIDTI), based on a residual network and classifier

  • The performance of heterogeneous information integration for DTI prediction (HIDTI) was evaluated for both cases when heterogeneous information was available for the unseen drugs and when heterogeneous information could only be predicted for the unseen drugs

  • Predicting DTIs is an essential task in drug discovery and development, and can further help in elucidating the mechanisms of biological processes related to drugs

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Summary

Objectives

We aimed to develop an approach that can predict DTIs by learning feature vectors from heterogeneous information

Methods
Results
Conclusion

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