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The Virtual Screening of the Drug Protein with a Few Crystal Structures Based on the Adaboost-SVM

Using the theory of machine learning to assist the virtual screening (VS) has been an effective plan. However, the quality of the training set may reduce because of mixing with the wrong docking poses and it will affect the screening efficiencies. To solve this problem, we present a method using the...

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Detalles Bibliográficos
Autores principales: Wang, Meng-yu, Li, Peng, Qiao, Pei-li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834164/
https://www.ncbi.nlm.nih.gov/pubmed/27127534
http://dx.doi.org/10.1155/2016/4809831
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author Wang, Meng-yu
Li, Peng
Qiao, Pei-li
author_facet Wang, Meng-yu
Li, Peng
Qiao, Pei-li
author_sort Wang, Meng-yu
collection PubMed
description Using the theory of machine learning to assist the virtual screening (VS) has been an effective plan. However, the quality of the training set may reduce because of mixing with the wrong docking poses and it will affect the screening efficiencies. To solve this problem, we present a method using the ensemble learning to improve the support vector machine to process the generated protein-ligand interaction fingerprint (IFP). By combining multiple classifiers, ensemble learning is able to avoid the limitations of the single classifier's performance and obtain better generalization. According to the research of virtual screening experiment with SRC and Cathepsin K as the target, the results show that the ensemble learning method can effectively reduce the error because the sample quality is not high and improve the effect of the whole virtual screening process.
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spelling pubmed-48341642016-04-28 The Virtual Screening of the Drug Protein with a Few Crystal Structures Based on the Adaboost-SVM Wang, Meng-yu Li, Peng Qiao, Pei-li Comput Math Methods Med Research Article Using the theory of machine learning to assist the virtual screening (VS) has been an effective plan. However, the quality of the training set may reduce because of mixing with the wrong docking poses and it will affect the screening efficiencies. To solve this problem, we present a method using the ensemble learning to improve the support vector machine to process the generated protein-ligand interaction fingerprint (IFP). By combining multiple classifiers, ensemble learning is able to avoid the limitations of the single classifier's performance and obtain better generalization. According to the research of virtual screening experiment with SRC and Cathepsin K as the target, the results show that the ensemble learning method can effectively reduce the error because the sample quality is not high and improve the effect of the whole virtual screening process. Hindawi Publishing Corporation 2016 2016-04-03 /pmc/articles/PMC4834164/ /pubmed/27127534 http://dx.doi.org/10.1155/2016/4809831 Text en Copyright © 2016 Meng-yu Wang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Meng-yu
Li, Peng
Qiao, Pei-li
The Virtual Screening of the Drug Protein with a Few Crystal Structures Based on the Adaboost-SVM
title The Virtual Screening of the Drug Protein with a Few Crystal Structures Based on the Adaboost-SVM
title_full The Virtual Screening of the Drug Protein with a Few Crystal Structures Based on the Adaboost-SVM
title_fullStr The Virtual Screening of the Drug Protein with a Few Crystal Structures Based on the Adaboost-SVM
title_full_unstemmed The Virtual Screening of the Drug Protein with a Few Crystal Structures Based on the Adaboost-SVM
title_short The Virtual Screening of the Drug Protein with a Few Crystal Structures Based on the Adaboost-SVM
title_sort virtual screening of the drug protein with a few crystal structures based on the adaboost-svm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834164/
https://www.ncbi.nlm.nih.gov/pubmed/27127534
http://dx.doi.org/10.1155/2016/4809831
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