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PCLPred: A Bioinformatics Method for Predicting Protein–Protein Interactions by Combining Relevance Vector Machine Model with Low-Rank Matrix Approximation
Protein–protein interactions (PPI) are key to protein functions and regulations within the cell cycle, DNA replication, and cellular signaling. Therefore, detecting whether a pair of proteins interact is of great importance for the study of molecular biology. As researchers have become aware of the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979371/ https://www.ncbi.nlm.nih.gov/pubmed/29596363 http://dx.doi.org/10.3390/ijms19041029 |
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author | Li, Li-Ping Wang, Yan-Bin You, Zhu-Hong Li, Yang An, Ji-Yong |
author_facet | Li, Li-Ping Wang, Yan-Bin You, Zhu-Hong Li, Yang An, Ji-Yong |
author_sort | Li, Li-Ping |
collection | PubMed |
description | Protein–protein interactions (PPI) are key to protein functions and regulations within the cell cycle, DNA replication, and cellular signaling. Therefore, detecting whether a pair of proteins interact is of great importance for the study of molecular biology. As researchers have become aware of the importance of computational methods in predicting PPIs, many techniques have been developed for performing this task computationally. However, there are few technologies that really meet the needs of their users. In this paper, we develop a novel and efficient sequence-based method for predicting PPIs. The evolutionary features are extracted from the position-specific scoring matrix (PSSM) of protein. The features are then fed into a robust relevance vector machine (RVM) classifier to distinguish between the interacting and non-interacting protein pairs. In order to verify the performance of our method, five-fold cross-validation tests are performed on the Saccharomyces cerevisiae dataset. A high accuracy of 94.56%, with 94.79% sensitivity at 94.36% precision, was obtained. The experimental results illustrated that the proposed approach can extract the most significant features from each protein sequence and can be a bright and meaningful tool for the research of proteomics. |
format | Online Article Text |
id | pubmed-5979371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-59793712018-06-10 PCLPred: A Bioinformatics Method for Predicting Protein–Protein Interactions by Combining Relevance Vector Machine Model with Low-Rank Matrix Approximation Li, Li-Ping Wang, Yan-Bin You, Zhu-Hong Li, Yang An, Ji-Yong Int J Mol Sci Article Protein–protein interactions (PPI) are key to protein functions and regulations within the cell cycle, DNA replication, and cellular signaling. Therefore, detecting whether a pair of proteins interact is of great importance for the study of molecular biology. As researchers have become aware of the importance of computational methods in predicting PPIs, many techniques have been developed for performing this task computationally. However, there are few technologies that really meet the needs of their users. In this paper, we develop a novel and efficient sequence-based method for predicting PPIs. The evolutionary features are extracted from the position-specific scoring matrix (PSSM) of protein. The features are then fed into a robust relevance vector machine (RVM) classifier to distinguish between the interacting and non-interacting protein pairs. In order to verify the performance of our method, five-fold cross-validation tests are performed on the Saccharomyces cerevisiae dataset. A high accuracy of 94.56%, with 94.79% sensitivity at 94.36% precision, was obtained. The experimental results illustrated that the proposed approach can extract the most significant features from each protein sequence and can be a bright and meaningful tool for the research of proteomics. MDPI 2018-03-29 /pmc/articles/PMC5979371/ /pubmed/29596363 http://dx.doi.org/10.3390/ijms19041029 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Li-Ping Wang, Yan-Bin You, Zhu-Hong Li, Yang An, Ji-Yong PCLPred: A Bioinformatics Method for Predicting Protein–Protein Interactions by Combining Relevance Vector Machine Model with Low-Rank Matrix Approximation |
title | PCLPred: A Bioinformatics Method for Predicting Protein–Protein Interactions by Combining Relevance Vector Machine Model with Low-Rank Matrix Approximation |
title_full | PCLPred: A Bioinformatics Method for Predicting Protein–Protein Interactions by Combining Relevance Vector Machine Model with Low-Rank Matrix Approximation |
title_fullStr | PCLPred: A Bioinformatics Method for Predicting Protein–Protein Interactions by Combining Relevance Vector Machine Model with Low-Rank Matrix Approximation |
title_full_unstemmed | PCLPred: A Bioinformatics Method for Predicting Protein–Protein Interactions by Combining Relevance Vector Machine Model with Low-Rank Matrix Approximation |
title_short | PCLPred: A Bioinformatics Method for Predicting Protein–Protein Interactions by Combining Relevance Vector Machine Model with Low-Rank Matrix Approximation |
title_sort | pclpred: a bioinformatics method for predicting protein–protein interactions by combining relevance vector machine model with low-rank matrix approximation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979371/ https://www.ncbi.nlm.nih.gov/pubmed/29596363 http://dx.doi.org/10.3390/ijms19041029 |
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