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iGRLDTI: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network

MOTIVATION: The task of predicting drug–target interactions (DTIs) plays a significant role in facilitating the development of novel drug discovery. Compared with laboratory-based approaches, computational methods proposed for DTI prediction are preferred due to their high-efficiency and low-cost ad...

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Autores principales: Zhao, Bo-Wei, Su, Xiao-Rui, Hu, Peng-Wei, Huang, Yu-An, You, Zhu-Hong, Hu, Lun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397422/
https://www.ncbi.nlm.nih.gov/pubmed/37505483
http://dx.doi.org/10.1093/bioinformatics/btad451
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author Zhao, Bo-Wei
Su, Xiao-Rui
Hu, Peng-Wei
Huang, Yu-An
You, Zhu-Hong
Hu, Lun
author_facet Zhao, Bo-Wei
Su, Xiao-Rui
Hu, Peng-Wei
Huang, Yu-An
You, Zhu-Hong
Hu, Lun
author_sort Zhao, Bo-Wei
collection PubMed
description MOTIVATION: The task of predicting drug–target interactions (DTIs) plays a significant role in facilitating the development of novel drug discovery. Compared with laboratory-based approaches, computational methods proposed for DTI prediction are preferred due to their high-efficiency and low-cost advantages. Recently, much attention has been attracted to apply different graph neural network (GNN) models to discover underlying DTIs from heterogeneous biological information network (HBIN). Although GNN-based prediction methods achieve better performance, they are prone to encounter the over-smoothing simulation when learning the latent representations of drugs and targets with their rich neighborhood information in HBIN, and thereby reduce the discriminative ability in DTI prediction. RESULTS: In this work, an improved graph representation learning method, namely iGRLDTI, is proposed to address the above issue by better capturing more discriminative representations of drugs and targets in a latent feature space. Specifically, iGRLDTI first constructs an HBIN by integrating the biological knowledge of drugs and targets with their interactions. After that, it adopts a node-dependent local smoothing strategy to adaptively decide the propagation depth of each biomolecule in HBIN, thus significantly alleviating over-smoothing by enhancing the discriminative ability of feature representations of drugs and targets. Finally, a Gradient Boosting Decision Tree classifier is used by iGRLDTI to predict novel DTIs. Experimental results demonstrate that iGRLDTI yields better performance that several state-of-the-art computational methods on the benchmark dataset. Besides, our case study indicates that iGRLDTI can successfully identify novel DTIs with more distinguishable features of drugs and targets. AVAILABILITY AND IMPLEMENTATION: Python codes and dataset are available at https://github.com/stevejobws/iGRLDTI/.
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spelling pubmed-103974222023-08-04 iGRLDTI: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network Zhao, Bo-Wei Su, Xiao-Rui Hu, Peng-Wei Huang, Yu-An You, Zhu-Hong Hu, Lun Bioinformatics Original Paper MOTIVATION: The task of predicting drug–target interactions (DTIs) plays a significant role in facilitating the development of novel drug discovery. Compared with laboratory-based approaches, computational methods proposed for DTI prediction are preferred due to their high-efficiency and low-cost advantages. Recently, much attention has been attracted to apply different graph neural network (GNN) models to discover underlying DTIs from heterogeneous biological information network (HBIN). Although GNN-based prediction methods achieve better performance, they are prone to encounter the over-smoothing simulation when learning the latent representations of drugs and targets with their rich neighborhood information in HBIN, and thereby reduce the discriminative ability in DTI prediction. RESULTS: In this work, an improved graph representation learning method, namely iGRLDTI, is proposed to address the above issue by better capturing more discriminative representations of drugs and targets in a latent feature space. Specifically, iGRLDTI first constructs an HBIN by integrating the biological knowledge of drugs and targets with their interactions. After that, it adopts a node-dependent local smoothing strategy to adaptively decide the propagation depth of each biomolecule in HBIN, thus significantly alleviating over-smoothing by enhancing the discriminative ability of feature representations of drugs and targets. Finally, a Gradient Boosting Decision Tree classifier is used by iGRLDTI to predict novel DTIs. Experimental results demonstrate that iGRLDTI yields better performance that several state-of-the-art computational methods on the benchmark dataset. Besides, our case study indicates that iGRLDTI can successfully identify novel DTIs with more distinguishable features of drugs and targets. AVAILABILITY AND IMPLEMENTATION: Python codes and dataset are available at https://github.com/stevejobws/iGRLDTI/. Oxford University Press 2023-07-28 /pmc/articles/PMC10397422/ /pubmed/37505483 http://dx.doi.org/10.1093/bioinformatics/btad451 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Zhao, Bo-Wei
Su, Xiao-Rui
Hu, Peng-Wei
Huang, Yu-An
You, Zhu-Hong
Hu, Lun
iGRLDTI: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network
title iGRLDTI: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network
title_full iGRLDTI: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network
title_fullStr iGRLDTI: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network
title_full_unstemmed iGRLDTI: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network
title_short iGRLDTI: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network
title_sort igrldti: an improved graph representation learning method for predicting drug–target interactions over heterogeneous biological information network
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397422/
https://www.ncbi.nlm.nih.gov/pubmed/37505483
http://dx.doi.org/10.1093/bioinformatics/btad451
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