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CardioTox net: a robust predictor for hERG channel blockade based on deep learning meta-feature ensembles

MOTIVATION: Ether-a-go-go-related gene (hERG) channel blockade by small molecules is a big concern during drug development in the pharmaceutical industry. Blockade of hERG channels may cause prolonged QT intervals that potentially could lead to cardiotoxicity. Various in-silico techniques including...

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Autores principales: Karim, Abdul, Lee, Matthew, Balle, Thomas, Sattar, Abdul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365955/
https://www.ncbi.nlm.nih.gov/pubmed/34399849
http://dx.doi.org/10.1186/s13321-021-00541-z
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author Karim, Abdul
Lee, Matthew
Balle, Thomas
Sattar, Abdul
author_facet Karim, Abdul
Lee, Matthew
Balle, Thomas
Sattar, Abdul
author_sort Karim, Abdul
collection PubMed
description MOTIVATION: Ether-a-go-go-related gene (hERG) channel blockade by small molecules is a big concern during drug development in the pharmaceutical industry. Blockade of hERG channels may cause prolonged QT intervals that potentially could lead to cardiotoxicity. Various in-silico techniques including deep learning models are widely used to screen out small molecules with potential hERG related toxicity. Most of the published deep learning methods utilize a single type of features which might restrict their performance. Methods based on more than one type of features such as DeepHIT struggle with the aggregation of extracted information. DeepHIT shows better performance when evaluated against one or two accuracy metrics such as negative predictive value (NPV) and sensitivity (SEN) but struggle when evaluated against others such as Matthew correlation coefficient (MCC), accuracy (ACC), positive predictive value (PPV) and specificity (SPE). Therefore, there is a need for a method that can efficiently aggregate information gathered from models based on different chemical representations and boost hERG toxicity prediction over a range of performance metrics. RESULTS: In this paper, we propose a deep learning framework based on step-wise training to predict hERG channel blocking activity of small molecules. Our approach utilizes five individual deep learning base models with their respective base features and a separate neural network to combine the outputs of the five base models. By using three external independent test sets with potency activity of IC(50) at a threshold of 10 [Formula: see text] m, our method achieves better performance for a combination of classification metrics. We also investigate the effective aggregation of chemical information extracted for robust hERG activity prediction. In summary, CardioTox net can serve as a robust tool for screening small molecules for hERG channel blockade in drug discovery pipelines and performs better than previously reported methods on a range of classification metrics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13321-021-00541-z.
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spelling pubmed-83659552021-08-17 CardioTox net: a robust predictor for hERG channel blockade based on deep learning meta-feature ensembles Karim, Abdul Lee, Matthew Balle, Thomas Sattar, Abdul J Cheminform Research Article MOTIVATION: Ether-a-go-go-related gene (hERG) channel blockade by small molecules is a big concern during drug development in the pharmaceutical industry. Blockade of hERG channels may cause prolonged QT intervals that potentially could lead to cardiotoxicity. Various in-silico techniques including deep learning models are widely used to screen out small molecules with potential hERG related toxicity. Most of the published deep learning methods utilize a single type of features which might restrict their performance. Methods based on more than one type of features such as DeepHIT struggle with the aggregation of extracted information. DeepHIT shows better performance when evaluated against one or two accuracy metrics such as negative predictive value (NPV) and sensitivity (SEN) but struggle when evaluated against others such as Matthew correlation coefficient (MCC), accuracy (ACC), positive predictive value (PPV) and specificity (SPE). Therefore, there is a need for a method that can efficiently aggregate information gathered from models based on different chemical representations and boost hERG toxicity prediction over a range of performance metrics. RESULTS: In this paper, we propose a deep learning framework based on step-wise training to predict hERG channel blocking activity of small molecules. Our approach utilizes five individual deep learning base models with their respective base features and a separate neural network to combine the outputs of the five base models. By using three external independent test sets with potency activity of IC(50) at a threshold of 10 [Formula: see text] m, our method achieves better performance for a combination of classification metrics. We also investigate the effective aggregation of chemical information extracted for robust hERG activity prediction. In summary, CardioTox net can serve as a robust tool for screening small molecules for hERG channel blockade in drug discovery pipelines and performs better than previously reported methods on a range of classification metrics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13321-021-00541-z. Springer International Publishing 2021-08-16 /pmc/articles/PMC8365955/ /pubmed/34399849 http://dx.doi.org/10.1186/s13321-021-00541-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Karim, Abdul
Lee, Matthew
Balle, Thomas
Sattar, Abdul
CardioTox net: a robust predictor for hERG channel blockade based on deep learning meta-feature ensembles
title CardioTox net: a robust predictor for hERG channel blockade based on deep learning meta-feature ensembles
title_full CardioTox net: a robust predictor for hERG channel blockade based on deep learning meta-feature ensembles
title_fullStr CardioTox net: a robust predictor for hERG channel blockade based on deep learning meta-feature ensembles
title_full_unstemmed CardioTox net: a robust predictor for hERG channel blockade based on deep learning meta-feature ensembles
title_short CardioTox net: a robust predictor for hERG channel blockade based on deep learning meta-feature ensembles
title_sort cardiotox net: a robust predictor for herg channel blockade based on deep learning meta-feature ensembles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365955/
https://www.ncbi.nlm.nih.gov/pubmed/34399849
http://dx.doi.org/10.1186/s13321-021-00541-z
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