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Modeling of the hERG K+ Channel Blockage Using Online Chemical Database and Modeling Environment (OCHEM)
Xiao Li1,2, Yuan Zhang2, Huanhuan Li2
1Beijing Computing Center, Beijing Academy of Science and Technology, 7 Fengxian road, Beijing, 100094, China.
Insights
Predicting human ether-a-go-go related gene (hERG) channel blockage is crucial for drug safety. This study developed accurate consensus models using machine learning to identify potential cardiotoxicity early in drug discovery.
Area of Science:
- Computational chemistry
- Pharmacology
- Toxicology
Background:
- The human ether-a-go-go related gene (hERG) K+ channel is vital for cardiac action potential.
- hERG channel blockade can lead to long QT syndrome (LQTS) and sudden cardiac death, causing drug recalls.
Purpose of the Study:
- To develop reliable computational models for predicting hERG channel blockage.
- To facilitate early-stage identification of potential cardiotoxicity in drug discovery.
Main Methods:
- Assembled a dataset of 3721 compounds with hERG inhibition data.
- Utilized the Online Chemical Modeling Environment (OCHEM) for machine learning model development.
- Generated consensus models by combining top-performing individual classification models.
Main Results:
- Consensus models significantly outperformed individual models in cross-validation and external validation.
- Consensus model II achieved 89.5% prediction accuracy and a 0.670 MCC on external validation.
- The developed models demonstrate superior predictive power compared to previous studies.
Conclusions:
- Machine learning-based consensus models are effective for predicting hERG channel blockage.
- These models can significantly aid in the early assessment of drug-induced cardiotoxicity.
- The models and datasets are publicly available for further research and application.
Abstract:
Human ether-a-go-go related gene (hERG) K+ channel plays an important role in cardiac action potential. Blockage of hERG channel may result in long QT syndrome (LQTS), even cause sudden cardiac death. Many drugs have been withdrawn from the market because of the serious hERG-related cardiotoxicity. Therefore, it is quite essential to estimate the chemical blockage of hERG in the early stage of drug discovery. In this study, a diverse set of 3721 compounds with hERG inhibition data was assembled from literature. Then, we make full use of the Online Chemical Modeling Environment (OCHEM), which supplies rich machine learning methods and descriptor sets, to build a series of classification models for hERG blockage. We also generated two consensus models based on the top-performing individual models. The consensus models performed much better than the individual models both on 5-fold cross validation and external validation. Especially, consensus model II yielded the prediction accuracy of 89.5 % and MCC of 0.670 on external validation. This result indicated that the predictive power of consensus model II should be stronger than most of the previously reported models. The 17 top-performing individual models and the consensus models and the data sets used for model development are available at https://ochem.eu/article/103592.
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