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PMLPR: A novel method for predicting subcellular localization based on recommender systems

The importance of protein subcellular localization problem is due to the importance of protein’s functions in different cell parts. Moreover, prediction of subcellular locations helps to identify the potential molecular targets for drugs and has an important role in genome annotation. Most of the ex...

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Autores principales: Mirzaei Mehrabad, Elnaz, Hassanzadeh, Reza, Eslahchi, Changiz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089892/
https://www.ncbi.nlm.nih.gov/pubmed/30104743
http://dx.doi.org/10.1038/s41598-018-30394-w
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author Mirzaei Mehrabad, Elnaz
Hassanzadeh, Reza
Eslahchi, Changiz
author_facet Mirzaei Mehrabad, Elnaz
Hassanzadeh, Reza
Eslahchi, Changiz
author_sort Mirzaei Mehrabad, Elnaz
collection PubMed
description The importance of protein subcellular localization problem is due to the importance of protein’s functions in different cell parts. Moreover, prediction of subcellular locations helps to identify the potential molecular targets for drugs and has an important role in genome annotation. Most of the existing prediction methods assign only one location for each protein. But, since some proteins move between different subcellular locations, they can have multiple locations. In recent years, some multiple location predictors have been introduced. However, their performances are not accurate enough and there is much room for improvement. In this paper, we introduced a method, PMLPR, to predict locations for a protein. PMLPR predicts a list of locations for each protein based on recommender systems and it can properly overcome the multiple location prediction problem. For evaluating the performance of PMLPR, we considered six datasets RAT, FLY, HUMAN, Du et al., DBMLoc and Höglund. The performance of this algorithm is compared with six state-of-the-art algorithms, YLoc, WOLF-PSORT, prediction channel, MDLoc, Du et al. and MultiLoc2-HighRes. The results indicate that our proposed method is significantly superior on RAT and Fly proteins, and decent on HUMAN proteins. Moreover, on the datasets introduced by Du et al., DBMLoc and Höglund, PMLPR has comparable results. For the case study, we applied the algorithms on 8 proteins which are important in cancer research. The results of comparison with other methods indicate the efficiency of PMLPR.
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spelling pubmed-60898922018-08-17 PMLPR: A novel method for predicting subcellular localization based on recommender systems Mirzaei Mehrabad, Elnaz Hassanzadeh, Reza Eslahchi, Changiz Sci Rep Article The importance of protein subcellular localization problem is due to the importance of protein’s functions in different cell parts. Moreover, prediction of subcellular locations helps to identify the potential molecular targets for drugs and has an important role in genome annotation. Most of the existing prediction methods assign only one location for each protein. But, since some proteins move between different subcellular locations, they can have multiple locations. In recent years, some multiple location predictors have been introduced. However, their performances are not accurate enough and there is much room for improvement. In this paper, we introduced a method, PMLPR, to predict locations for a protein. PMLPR predicts a list of locations for each protein based on recommender systems and it can properly overcome the multiple location prediction problem. For evaluating the performance of PMLPR, we considered six datasets RAT, FLY, HUMAN, Du et al., DBMLoc and Höglund. The performance of this algorithm is compared with six state-of-the-art algorithms, YLoc, WOLF-PSORT, prediction channel, MDLoc, Du et al. and MultiLoc2-HighRes. The results indicate that our proposed method is significantly superior on RAT and Fly proteins, and decent on HUMAN proteins. Moreover, on the datasets introduced by Du et al., DBMLoc and Höglund, PMLPR has comparable results. For the case study, we applied the algorithms on 8 proteins which are important in cancer research. The results of comparison with other methods indicate the efficiency of PMLPR. Nature Publishing Group UK 2018-08-13 /pmc/articles/PMC6089892/ /pubmed/30104743 http://dx.doi.org/10.1038/s41598-018-30394-w Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mirzaei Mehrabad, Elnaz
Hassanzadeh, Reza
Eslahchi, Changiz
PMLPR: A novel method for predicting subcellular localization based on recommender systems
title PMLPR: A novel method for predicting subcellular localization based on recommender systems
title_full PMLPR: A novel method for predicting subcellular localization based on recommender systems
title_fullStr PMLPR: A novel method for predicting subcellular localization based on recommender systems
title_full_unstemmed PMLPR: A novel method for predicting subcellular localization based on recommender systems
title_short PMLPR: A novel method for predicting subcellular localization based on recommender systems
title_sort pmlpr: a novel method for predicting subcellular localization based on recommender systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089892/
https://www.ncbi.nlm.nih.gov/pubmed/30104743
http://dx.doi.org/10.1038/s41598-018-30394-w
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