Lihong Peng 1,2,3 , Bo Liao 1 , Wen Zhu 1 , Zejun Li 1 . Show Affiliations »
Abstract
BACKGROUND: Inferring drug-target interaction (DTI) candidates for new drugs or targets without any interaction information is a critical challenge for modern drug design and discovery. Results from existing DTI inference methods indicate that these approaches necessitate further improvement. METHODS: In this paper, we developed a novel DTI identification model (PreNNDS) by integrating Neighbor interaction profiles, Nonnegative matrix factorization, Discriminative low-rank representation, and Sparse representation classification into a unified framework. RESULTS: AUPR values on four types of datasets show that PreNNDS can efficiently identify potential DTIs for new drugs or targets. We listed predicted top 20 drugs interacting with hsa1132 and hsa1124 and top 20 targets interacting with D00255 and D00195. CONCLUSIONS: PreNNDS can be applied to identify multi-target drugs and multi-drug resistance proteins, as well as to provide clues for microRNA-disease and gene-disease association prediction. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.
BACKGROUND: Inferring drug-target interaction (DTI) candidates for new drugs or targets without any interaction information is a critical challenge for modern drug design and discovery. Results from existing DTI inference methods indicate that these approaches necessitate further improvement. METHODS: In this paper, we developed a novel DTI identification model (PreNNDS) by integrating Neighbor interaction profiles, Nonnegative matrix factorization, Discriminative low-rank representation, and Sparse representation classification into a unified framework. RESULTS: AUPR values on four types of datasets show that PreNNDS can efficiently identify potential DTIs for new drugs or targets. We listed predicted top 20 drugs interacting with hsa1132 and hsa1124 and top 20 targets interacting with D00255 and D00195. CONCLUSIONS: PreNNDS can be applied to identify multi-target drugs and multi-drug resistance proteins, as well as to provide clues for microRNA-disease and gene-disease association prediction. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.
Keywords:
Drug-target interaction; discriminativezzm321990low-rank representation; neighbor interaction profile; new drugs or targets; nonnegative matrix factorization; sparse representation classification
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Year: 2018
PMID: 27829345 DOI: 10.2174/1389203718666161108100333
Source DB: PubMed Journal: Curr Protein Pept Sci ISSN: 1389-2037 Impact factor: 3.272