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Transfer learning for drug–target interaction prediction

MOTIVATION: Utilizing AI-driven approaches for drug–target interaction (DTI) prediction require large volumes of training data which are not available for the majority of target proteins. In this study, we investigate the use of deep transfer learning for the prediction of interactions between drug...

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Autores principales: Dalkıran, Alperen, Atakan, Ahmet, Rifaioğlu, Ahmet S, Martin, Maria J, Atalay, Rengül Çetin, Acar, Aybar C, Doğan, Tunca, Atalay, Volkan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311347/
https://www.ncbi.nlm.nih.gov/pubmed/37387156
http://dx.doi.org/10.1093/bioinformatics/btad234
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author Dalkıran, Alperen
Atakan, Ahmet
Rifaioğlu, Ahmet S
Martin, Maria J
Atalay, Rengül Çetin
Acar, Aybar C
Doğan, Tunca
Atalay, Volkan
author_facet Dalkıran, Alperen
Atakan, Ahmet
Rifaioğlu, Ahmet S
Martin, Maria J
Atalay, Rengül Çetin
Acar, Aybar C
Doğan, Tunca
Atalay, Volkan
author_sort Dalkıran, Alperen
collection PubMed
description MOTIVATION: Utilizing AI-driven approaches for drug–target interaction (DTI) prediction require large volumes of training data which are not available for the majority of target proteins. In this study, we investigate the use of deep transfer learning for the prediction of interactions between drug candidate compounds and understudied target proteins with scarce training data. The idea here is to first train a deep neural network classifier with a generalized source training dataset of large size and then to reuse this pre-trained neural network as an initial configuration for re-training/fine-tuning purposes with a small-sized specialized target training dataset. To explore this idea, we selected six protein families that have critical importance in biomedicine: kinases, G-protein-coupled receptors (GPCRs), ion channels, nuclear receptors, proteases, and transporters. In two independent experiments, the protein families of transporters and nuclear receptors were individually set as the target datasets, while the remaining five families were used as the source datasets. Several size-based target family training datasets were formed in a controlled manner to assess the benefit provided by the transfer learning approach. RESULTS: Here, we present a systematic evaluation of our approach by pre-training a feed-forward neural network with source training datasets and applying different modes of transfer learning from the pre-trained source network to a target dataset. The performance of deep transfer learning is evaluated and compared with that of training the same deep neural network from scratch. We found that when the training dataset contains fewer than 100 compounds, transfer learning outperforms the conventional strategy of training the system from scratch, suggesting that transfer learning is advantageous for predicting binders to under-studied targets. AVAILABILITY AND IMPLEMENTATION: The source code and datasets are available at https://github.com/cansyl/TransferLearning4DTI. Our web-based service containing the ready-to-use pre-trained models is accessible at https://tl4dti.kansil.org.
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spelling pubmed-103113472023-07-01 Transfer learning for drug–target interaction prediction Dalkıran, Alperen Atakan, Ahmet Rifaioğlu, Ahmet S Martin, Maria J Atalay, Rengül Çetin Acar, Aybar C Doğan, Tunca Atalay, Volkan Bioinformatics Biomedical Informatics MOTIVATION: Utilizing AI-driven approaches for drug–target interaction (DTI) prediction require large volumes of training data which are not available for the majority of target proteins. In this study, we investigate the use of deep transfer learning for the prediction of interactions between drug candidate compounds and understudied target proteins with scarce training data. The idea here is to first train a deep neural network classifier with a generalized source training dataset of large size and then to reuse this pre-trained neural network as an initial configuration for re-training/fine-tuning purposes with a small-sized specialized target training dataset. To explore this idea, we selected six protein families that have critical importance in biomedicine: kinases, G-protein-coupled receptors (GPCRs), ion channels, nuclear receptors, proteases, and transporters. In two independent experiments, the protein families of transporters and nuclear receptors were individually set as the target datasets, while the remaining five families were used as the source datasets. Several size-based target family training datasets were formed in a controlled manner to assess the benefit provided by the transfer learning approach. RESULTS: Here, we present a systematic evaluation of our approach by pre-training a feed-forward neural network with source training datasets and applying different modes of transfer learning from the pre-trained source network to a target dataset. The performance of deep transfer learning is evaluated and compared with that of training the same deep neural network from scratch. We found that when the training dataset contains fewer than 100 compounds, transfer learning outperforms the conventional strategy of training the system from scratch, suggesting that transfer learning is advantageous for predicting binders to under-studied targets. AVAILABILITY AND IMPLEMENTATION: The source code and datasets are available at https://github.com/cansyl/TransferLearning4DTI. Our web-based service containing the ready-to-use pre-trained models is accessible at https://tl4dti.kansil.org. Oxford University Press 2023-06-30 /pmc/articles/PMC10311347/ /pubmed/37387156 http://dx.doi.org/10.1093/bioinformatics/btad234 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 Biomedical Informatics
Dalkıran, Alperen
Atakan, Ahmet
Rifaioğlu, Ahmet S
Martin, Maria J
Atalay, Rengül Çetin
Acar, Aybar C
Doğan, Tunca
Atalay, Volkan
Transfer learning for drug–target interaction prediction
title Transfer learning for drug–target interaction prediction
title_full Transfer learning for drug–target interaction prediction
title_fullStr Transfer learning for drug–target interaction prediction
title_full_unstemmed Transfer learning for drug–target interaction prediction
title_short Transfer learning for drug–target interaction prediction
title_sort transfer learning for drug–target interaction prediction
topic Biomedical Informatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311347/
https://www.ncbi.nlm.nih.gov/pubmed/37387156
http://dx.doi.org/10.1093/bioinformatics/btad234
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