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Inferring domain-domain interactions from protein-protein interactions in the complex network conformation

BACKGROUND: As protein domains are functional and structural units of proteins, a large proportion of protein-protein interactions (PPIs) are achieved by domain-domain interactions (DDIs), many computational efforts have been made to identify DDIs from experimental PPIs since high throughput technol...

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Autores principales: Chen, Chen, Zhao, Jun-Fei, Huang, Qiang, Wang, Rui-Sheng, Zhang, Xiang-Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403472/
https://www.ncbi.nlm.nih.gov/pubmed/23046795
http://dx.doi.org/10.1186/1752-0509-6-S1-S7
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author Chen, Chen
Zhao, Jun-Fei
Huang, Qiang
Wang, Rui-Sheng
Zhang, Xiang-Sun
author_facet Chen, Chen
Zhao, Jun-Fei
Huang, Qiang
Wang, Rui-Sheng
Zhang, Xiang-Sun
author_sort Chen, Chen
collection PubMed
description BACKGROUND: As protein domains are functional and structural units of proteins, a large proportion of protein-protein interactions (PPIs) are achieved by domain-domain interactions (DDIs), many computational efforts have been made to identify DDIs from experimental PPIs since high throughput technologies have produced a large number of PPIs for different species. These methods can be separated into two categories: deterministic and probabilistic. In deterministic methods, parsimony assumption has been utilized. Parsimony principle has been widely used in computational biology as the evolution of the nature is considered as a continuous optimization process. In the context of identifying DDIs, parsimony methods try to find a minimal set of DDIs that can explain the observed PPIs. This category of methods are promising since they can be formulated and solved easily. Besides, researches have shown that they can detect specific DDIs, which is often hard for many probabilistic methods. We notice that existing methods just view PPI networks as simply assembled by single interactions, but there is now ample evidence that PPI networks should be considered in a global (systematic) point of view for it exhibits general properties of complex networks, such as 'scale-free' and 'small-world'. RESULTS: In this work, we integrate this global point of view into the parsimony-based model. Particularly, prior knowledge is extracted from these global properties by plausible reasoning and then taken as input. We investigate the role of the added information extensively through numerical experiments. Results show that the proposed method has improved performance, which confirms the biological meanings of the extracted prior knowledge. CONCLUSIONS: This work provides us some clues for using these properties of complex networks in computational models and to some extent reveals the biological meanings underlying these general network properties.
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spelling pubmed-34034722012-07-27 Inferring domain-domain interactions from protein-protein interactions in the complex network conformation Chen, Chen Zhao, Jun-Fei Huang, Qiang Wang, Rui-Sheng Zhang, Xiang-Sun BMC Syst Biol Research BACKGROUND: As protein domains are functional and structural units of proteins, a large proportion of protein-protein interactions (PPIs) are achieved by domain-domain interactions (DDIs), many computational efforts have been made to identify DDIs from experimental PPIs since high throughput technologies have produced a large number of PPIs for different species. These methods can be separated into two categories: deterministic and probabilistic. In deterministic methods, parsimony assumption has been utilized. Parsimony principle has been widely used in computational biology as the evolution of the nature is considered as a continuous optimization process. In the context of identifying DDIs, parsimony methods try to find a minimal set of DDIs that can explain the observed PPIs. This category of methods are promising since they can be formulated and solved easily. Besides, researches have shown that they can detect specific DDIs, which is often hard for many probabilistic methods. We notice that existing methods just view PPI networks as simply assembled by single interactions, but there is now ample evidence that PPI networks should be considered in a global (systematic) point of view for it exhibits general properties of complex networks, such as 'scale-free' and 'small-world'. RESULTS: In this work, we integrate this global point of view into the parsimony-based model. Particularly, prior knowledge is extracted from these global properties by plausible reasoning and then taken as input. We investigate the role of the added information extensively through numerical experiments. Results show that the proposed method has improved performance, which confirms the biological meanings of the extracted prior knowledge. CONCLUSIONS: This work provides us some clues for using these properties of complex networks in computational models and to some extent reveals the biological meanings underlying these general network properties. BioMed Central 2012-07-16 /pmc/articles/PMC3403472/ /pubmed/23046795 http://dx.doi.org/10.1186/1752-0509-6-S1-S7 Text en Copyright ©2012 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chen, Chen
Zhao, Jun-Fei
Huang, Qiang
Wang, Rui-Sheng
Zhang, Xiang-Sun
Inferring domain-domain interactions from protein-protein interactions in the complex network conformation
title Inferring domain-domain interactions from protein-protein interactions in the complex network conformation
title_full Inferring domain-domain interactions from protein-protein interactions in the complex network conformation
title_fullStr Inferring domain-domain interactions from protein-protein interactions in the complex network conformation
title_full_unstemmed Inferring domain-domain interactions from protein-protein interactions in the complex network conformation
title_short Inferring domain-domain interactions from protein-protein interactions in the complex network conformation
title_sort inferring domain-domain interactions from protein-protein interactions in the complex network conformation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403472/
https://www.ncbi.nlm.nih.gov/pubmed/23046795
http://dx.doi.org/10.1186/1752-0509-6-S1-S7
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