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iBitter-Fuse: A Novel Sequence-Based Bitter Peptide Predictor by Fusing Multi-View Features

Accurate identification of bitter peptides is of great importance for better understanding their biochemical and biophysical properties. To date, machine learning-based methods have become effective approaches for providing a good avenue for identifying potential bitter peptides from large-scale pro...

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Autores principales: Charoenkwan, Phasit, Nantasenamat, Chanin, Hasan, Md. Mehedi, Moni, Mohammad Ali, Lio’, Pietro, Shoombuatong, Watshara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396555/
https://www.ncbi.nlm.nih.gov/pubmed/34445663
http://dx.doi.org/10.3390/ijms22168958
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author Charoenkwan, Phasit
Nantasenamat, Chanin
Hasan, Md. Mehedi
Moni, Mohammad Ali
Lio’, Pietro
Shoombuatong, Watshara
author_facet Charoenkwan, Phasit
Nantasenamat, Chanin
Hasan, Md. Mehedi
Moni, Mohammad Ali
Lio’, Pietro
Shoombuatong, Watshara
author_sort Charoenkwan, Phasit
collection PubMed
description Accurate identification of bitter peptides is of great importance for better understanding their biochemical and biophysical properties. To date, machine learning-based methods have become effective approaches for providing a good avenue for identifying potential bitter peptides from large-scale protein datasets. Although few machine learning-based predictors have been developed for identifying the bitterness of peptides, their prediction performances could be improved. In this study, we developed a new predictor (named iBitter-Fuse) for achieving more accurate identification of bitter peptides. In the proposed iBitter-Fuse, we have integrated a variety of feature encoding schemes for providing sufficient information from different aspects, namely consisting of compositional information and physicochemical properties. To enhance the predictive performance, the customized genetic algorithm utilizing self-assessment-report (GA-SAR) was employed for identifying informative features followed by inputting optimal ones into a support vector machine (SVM)-based classifier for developing the final model (iBitter-Fuse). Benchmarking experiments based on both 10-fold cross-validation and independent tests indicated that the iBitter-Fuse was able to achieve more accurate performance as compared to state-of-the-art methods. To facilitate the high-throughput identification of bitter peptides, the iBitter-Fuse web server was established and made freely available online. It is anticipated that the iBitter-Fuse will be a useful tool for aiding the discovery and de novo design of bitter peptides.
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spelling pubmed-83965552021-08-28 iBitter-Fuse: A Novel Sequence-Based Bitter Peptide Predictor by Fusing Multi-View Features Charoenkwan, Phasit Nantasenamat, Chanin Hasan, Md. Mehedi Moni, Mohammad Ali Lio’, Pietro Shoombuatong, Watshara Int J Mol Sci Article Accurate identification of bitter peptides is of great importance for better understanding their biochemical and biophysical properties. To date, machine learning-based methods have become effective approaches for providing a good avenue for identifying potential bitter peptides from large-scale protein datasets. Although few machine learning-based predictors have been developed for identifying the bitterness of peptides, their prediction performances could be improved. In this study, we developed a new predictor (named iBitter-Fuse) for achieving more accurate identification of bitter peptides. In the proposed iBitter-Fuse, we have integrated a variety of feature encoding schemes for providing sufficient information from different aspects, namely consisting of compositional information and physicochemical properties. To enhance the predictive performance, the customized genetic algorithm utilizing self-assessment-report (GA-SAR) was employed for identifying informative features followed by inputting optimal ones into a support vector machine (SVM)-based classifier for developing the final model (iBitter-Fuse). Benchmarking experiments based on both 10-fold cross-validation and independent tests indicated that the iBitter-Fuse was able to achieve more accurate performance as compared to state-of-the-art methods. To facilitate the high-throughput identification of bitter peptides, the iBitter-Fuse web server was established and made freely available online. It is anticipated that the iBitter-Fuse will be a useful tool for aiding the discovery and de novo design of bitter peptides. MDPI 2021-08-19 /pmc/articles/PMC8396555/ /pubmed/34445663 http://dx.doi.org/10.3390/ijms22168958 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Charoenkwan, Phasit
Nantasenamat, Chanin
Hasan, Md. Mehedi
Moni, Mohammad Ali
Lio’, Pietro
Shoombuatong, Watshara
iBitter-Fuse: A Novel Sequence-Based Bitter Peptide Predictor by Fusing Multi-View Features
title iBitter-Fuse: A Novel Sequence-Based Bitter Peptide Predictor by Fusing Multi-View Features
title_full iBitter-Fuse: A Novel Sequence-Based Bitter Peptide Predictor by Fusing Multi-View Features
title_fullStr iBitter-Fuse: A Novel Sequence-Based Bitter Peptide Predictor by Fusing Multi-View Features
title_full_unstemmed iBitter-Fuse: A Novel Sequence-Based Bitter Peptide Predictor by Fusing Multi-View Features
title_short iBitter-Fuse: A Novel Sequence-Based Bitter Peptide Predictor by Fusing Multi-View Features
title_sort ibitter-fuse: a novel sequence-based bitter peptide predictor by fusing multi-view features
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396555/
https://www.ncbi.nlm.nih.gov/pubmed/34445663
http://dx.doi.org/10.3390/ijms22168958
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