Skip Navigation


Bioinformatics Advance Access originally published online on July 15, 2009
Bioinformatics 2009 25(18):2397-2403; doi:10.1093/bioinformatics/btp433
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (Print PDF) Freely available
Right arrowOA All Versions of this Article:
25/18/2397    most recent
btp433v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Bleakley, K.
Right arrow Articles by Yamanishi, Y.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bleakley, K.
Right arrow Articles by Yamanishi, Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2009 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Supervised prediction of drug–target interactions using bipartite local models

Kevin Bleakley 1,2,3,* and Yoshihiro Yamanishi 1,2,3

1Mines ParisTech, Centre for Computational Biology, 35 rue Saint-Honoré, F-77305 Fontainebleau Cedex, 2Institut Curie and 3INSERM, U900, F-75248, Paris, France

*To whom correspondence should be addressed.


   Abstract

Motivation: In silico prediction of drug–target interactions from heterogeneous biological data is critical in the search for drugs for known diseases. This problem is currently being attacked from many different points of view, a strong indication of its current importance. Precisely, being able to predict new drug–target interactions with both high precision and accuracy is the holy grail, a fundamental requirement for in silico methods to be useful in a biological setting. This, however, remains extremely challenging due to, amongst other things, the rarity of known drug–target interactions.

Results: We propose a novel supervised inference method to predict unknown drug–target interactions, represented as a bipartite graph. We use this method, known as bipartite local models to first predict target proteins of a given drug, then to predict drugs targeting a given protein. This gives two independent predictions for each putative drug–target interaction, which we show can be combined to give a definitive prediction for each interaction. We demonstrate the excellent performance of the proposed method in the prediction of four classes of drug–target interaction networks involving enzymes, ion channels, G protein-coupled receptors (GPCRs) and nuclear receptors in human. This enables us to suggest a number of new potential drug–target interactions.

Availability: An implementation of the proposed algorithm is available upon request from the authors. Datasets and all prediction results are available at http://cbio.ensmp.fr/~yyamanishi/bipartitelocal/.

Contact: kevbleakley{at}gmail.com

Supplementary information: Supplementary data are available at Bioinformatics online.

Associate Editor: Olga Troyanskaya


Received on March 17, 2009; revised on June 12, 2009; accepted on July 7, 2009

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.