Identifying Drug-Target Interactions with Decision Templates

Title:Identifying Drug-Target Interactions with Decision Templates

Volume: 19 Issue: 5

Author(s): Xiao-Ying Yan and Shao-Wu Zhang*

Affiliation:

• Key Laboratory of Information Fusion Technology of Ministry of Education, School of Automation, Northwestern Polytechnical University, Xi'an, 710072,China

Keywords: Drug-target interaction, decision template, drug similarity, target similarity, gene ontology, pathway, identification.

Abstract: Background: During the development process of new drugs, identification of the drug-target interactions wins primary concerns. However, the chemical or biological experiments bear the limitation in coverage as well as the huge cost of both time and money. Based on drug similarity and target similarity, chemogenomic methods can be able to predict potential drug-target interactions (DTIs) on a large scale and have no luxurious need about target structures or ligand entries.

Objective: In order to reflect the cases that the drugs having variant structures interact with common targets and the targets having dissimilar sequences interact with same drugs. In addition, though several other similarity metrics have been developed to predict DTIs, the combination of multiple similarity metrics (especially heterogeneous similarities) is too naïve to sufficiently explore the multiple similarities.

Method: In this paper, based on Gene Ontology and pathway annotation, we introduce two novel target similarity metrics to address above issues. More importantly, we propose a more effective strategy via decision template to integrate multiple classifiers designed with multiple similarity metrics.

Results: In the scenarios that predict existing targets for new drugs and predict approved drugs for new protein targets, the results on the DTI benchmark datasets show that our target similarity metrics are able to enhance the predictive accuracies in two scenarios. And the elaborate fusion strategy of multiple classifiers has better predictive power than the naïve combination of multiple similarity metrics.

Conclusion: Compared with other two state-of-the-art approaches on the four popular benchmark datasets of binary drug-target interactions, our method achieves the best results in terms of AUC and AUPR for predicting available targets for new drugs (S2), and predicting approved drugs for new protein targets (S3).These results demonstrate that our method can effectively predict the drug-target interactions. The software package can freely available at https://github.com/NwpuSY/DT_all.git for academic users

Cite this article as:

Yan Xiao-Ying and Zhang Shao-Wu*, Identifying Drug-Target Interactions with Decision Templates, Current Protein & Peptide Science 2018; 19 (5) . https://dx.doi.org/10.2174/1389203718666161108101118

DOI https://dx.doi.org/10.2174/1389203718666161108101118	Print ISSN 1389-2037
Publisher Name Bentham Science Publisher	Online ISSN 1875-5550