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An iteration model for identifying essential proteins by combining comprehensive PPI network with biological information

BACKGROUND: Essential proteins have great impacts on cell survival and development, and played important roles in disease analysis and new drug design. However, since it is inefficient and costly to identify essential proteins by using biological experiments, then there is an urgent need for automat...

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Autores principales: Li, Shiyuan, Zhang, Zhen, Li, Xueyong, Tan, Yihong, Wang, Lei, Chen, Zhiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425031/
https://www.ncbi.nlm.nih.gov/pubmed/34496745
http://dx.doi.org/10.1186/s12859-021-04300-7
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author Li, Shiyuan
Zhang, Zhen
Li, Xueyong
Tan, Yihong
Wang, Lei
Chen, Zhiping
author_facet Li, Shiyuan
Zhang, Zhen
Li, Xueyong
Tan, Yihong
Wang, Lei
Chen, Zhiping
author_sort Li, Shiyuan
collection PubMed
description BACKGROUND: Essential proteins have great impacts on cell survival and development, and played important roles in disease analysis and new drug design. However, since it is inefficient and costly to identify essential proteins by using biological experiments, then there is an urgent need for automated and accurate detection methods. In recent years, the recognition of essential proteins in protein interaction networks (PPI) has become a research hotspot, and many computational models for predicting essential proteins have been proposed successively. RESULTS: In order to achieve higher prediction performance, in this paper, a new prediction model called TGSO is proposed. In TGSO, a protein aggregation degree network is constructed first by adopting the node density measurement method for complex networks. And simultaneously, a protein co-expression interactive network is constructed by combining the gene expression information with the network connectivity, and a protein co-localization interaction network is constructed based on the subcellular localization data. And then, through integrating these three kinds of newly constructed networks, a comprehensive protein–protein interaction network will be obtained. Finally, based on the homology information, scores can be calculated out iteratively for different proteins, which can be utilized to estimate the importance of proteins effectively. Moreover, in order to evaluate the identification performance of TGSO, we have compared TGSO with 13 different latest competitive methods based on three kinds of yeast databases. And experimental results show that TGSO can achieve identification accuracies of 94%, 82% and 72% out of the top 1%, 5% and 10% candidate proteins respectively, which are to some degree superior to these state-of-the-art competitive models. CONCLUSIONS: We constructed a comprehensive interactive network based on multi-source data to reduce the noise and errors in the initial PPI, and combined with iterative methods to improve the accuracy of necessary protein prediction, and means that TGSO may be conducive to the future development of essential protein recognition as well.
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spelling pubmed-84250312021-09-10 An iteration model for identifying essential proteins by combining comprehensive PPI network with biological information Li, Shiyuan Zhang, Zhen Li, Xueyong Tan, Yihong Wang, Lei Chen, Zhiping BMC Bioinformatics Research Article BACKGROUND: Essential proteins have great impacts on cell survival and development, and played important roles in disease analysis and new drug design. However, since it is inefficient and costly to identify essential proteins by using biological experiments, then there is an urgent need for automated and accurate detection methods. In recent years, the recognition of essential proteins in protein interaction networks (PPI) has become a research hotspot, and many computational models for predicting essential proteins have been proposed successively. RESULTS: In order to achieve higher prediction performance, in this paper, a new prediction model called TGSO is proposed. In TGSO, a protein aggregation degree network is constructed first by adopting the node density measurement method for complex networks. And simultaneously, a protein co-expression interactive network is constructed by combining the gene expression information with the network connectivity, and a protein co-localization interaction network is constructed based on the subcellular localization data. And then, through integrating these three kinds of newly constructed networks, a comprehensive protein–protein interaction network will be obtained. Finally, based on the homology information, scores can be calculated out iteratively for different proteins, which can be utilized to estimate the importance of proteins effectively. Moreover, in order to evaluate the identification performance of TGSO, we have compared TGSO with 13 different latest competitive methods based on three kinds of yeast databases. And experimental results show that TGSO can achieve identification accuracies of 94%, 82% and 72% out of the top 1%, 5% and 10% candidate proteins respectively, which are to some degree superior to these state-of-the-art competitive models. CONCLUSIONS: We constructed a comprehensive interactive network based on multi-source data to reduce the noise and errors in the initial PPI, and combined with iterative methods to improve the accuracy of necessary protein prediction, and means that TGSO may be conducive to the future development of essential protein recognition as well. BioMed Central 2021-09-08 /pmc/articles/PMC8425031/ /pubmed/34496745 http://dx.doi.org/10.1186/s12859-021-04300-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Li, Shiyuan
Zhang, Zhen
Li, Xueyong
Tan, Yihong
Wang, Lei
Chen, Zhiping
An iteration model for identifying essential proteins by combining comprehensive PPI network with biological information
title An iteration model for identifying essential proteins by combining comprehensive PPI network with biological information
title_full An iteration model for identifying essential proteins by combining comprehensive PPI network with biological information
title_fullStr An iteration model for identifying essential proteins by combining comprehensive PPI network with biological information
title_full_unstemmed An iteration model for identifying essential proteins by combining comprehensive PPI network with biological information
title_short An iteration model for identifying essential proteins by combining comprehensive PPI network with biological information
title_sort iteration model for identifying essential proteins by combining comprehensive ppi network with biological information
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425031/
https://www.ncbi.nlm.nih.gov/pubmed/34496745
http://dx.doi.org/10.1186/s12859-021-04300-7
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