Bayesian statistical modelling of human protein interaction network incorporating protein disorder information

<p>Abstract</p> <p>Background</p> <p>We present a statistical method of analysis of biological networks based on the exponential random graph model, namely p2-model, as opposed to previous descriptive approaches. The model is capable to capture generic and structural pr...

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Main Authors: Eils Roland, Bulashevska Alla, Bulashevska Svetlana
Format: Article
Language:English
Published: BMC 2010-01-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/11/46
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spelling doaj-8b3d8a22ca3f434da171b68d8b2106702020-11-24T21:42:57ZengBMCBMC Bioinformatics1471-21052010-01-011114610.1186/1471-2105-11-46Bayesian statistical modelling of human protein interaction network incorporating protein disorder informationEils RolandBulashevska AllaBulashevska Svetlana<p>Abstract</p> <p>Background</p> <p>We present a statistical method of analysis of biological networks based on the exponential random graph model, namely p2-model, as opposed to previous descriptive approaches. The model is capable to capture generic and structural properties of a network as emergent from local interdependencies and uses a limited number of parameters. Here, we consider one global parameter capturing the density of edges in the network, and local parameters representing each node's contribution to the formation of edges in the network. The modelling suggests a novel definition of important nodes in the network, namely <it>social</it>, as revealed based on the local <it>sociality </it>parameters of the model. Moreover, the sociality parameters help to reveal organizational principles of the network. An inherent advantage of our approach is the possibility of hypotheses testing: <it>a priori </it>knowledge about biological properties of the nodes can be incorporated into the statistical model to investigate its influence on the structure of the network.</p> <p>Results</p> <p>We applied the statistical modelling to the human protein interaction network obtained with Y2H experiments. Bayesian approach for the estimation of the parameters was employed. We deduced <it>social </it>proteins, essential for the formation of the network, while incorporating into the model information on protein disorder. <it>Intrinsically disordered </it>are proteins which lack a well-defined three-dimensional structure under physiological conditions. We predicted the fold group (ordered or disordered) of proteins in the network from their primary sequences. The network analysis indicated that protein disorder has a positive effect on the connectivity of proteins in the network, but do not fully explains the interactivity.</p> <p>Conclusions</p> <p>The approach opens a perspective to study effects of biological properties of individual entities on the structure of biological networks.</p> http://www.biomedcentral.com/1471-2105/11/46
collection DOAJ
language English
format Article
sources DOAJ
author Eils Roland
Bulashevska Alla
Bulashevska Svetlana
spellingShingle Eils Roland
Bulashevska Alla
Bulashevska Svetlana
Bayesian statistical modelling of human protein interaction network incorporating protein disorder information
BMC Bioinformatics
author_facet Eils Roland
Bulashevska Alla
Bulashevska Svetlana
author_sort Eils Roland
title Bayesian statistical modelling of human protein interaction network incorporating protein disorder information
title_short Bayesian statistical modelling of human protein interaction network incorporating protein disorder information
title_full Bayesian statistical modelling of human protein interaction network incorporating protein disorder information
title_fullStr Bayesian statistical modelling of human protein interaction network incorporating protein disorder information
title_full_unstemmed Bayesian statistical modelling of human protein interaction network incorporating protein disorder information
title_sort bayesian statistical modelling of human protein interaction network incorporating protein disorder information
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2010-01-01
description <p>Abstract</p> <p>Background</p> <p>We present a statistical method of analysis of biological networks based on the exponential random graph model, namely p2-model, as opposed to previous descriptive approaches. The model is capable to capture generic and structural properties of a network as emergent from local interdependencies and uses a limited number of parameters. Here, we consider one global parameter capturing the density of edges in the network, and local parameters representing each node's contribution to the formation of edges in the network. The modelling suggests a novel definition of important nodes in the network, namely <it>social</it>, as revealed based on the local <it>sociality </it>parameters of the model. Moreover, the sociality parameters help to reveal organizational principles of the network. An inherent advantage of our approach is the possibility of hypotheses testing: <it>a priori </it>knowledge about biological properties of the nodes can be incorporated into the statistical model to investigate its influence on the structure of the network.</p> <p>Results</p> <p>We applied the statistical modelling to the human protein interaction network obtained with Y2H experiments. Bayesian approach for the estimation of the parameters was employed. We deduced <it>social </it>proteins, essential for the formation of the network, while incorporating into the model information on protein disorder. <it>Intrinsically disordered </it>are proteins which lack a well-defined three-dimensional structure under physiological conditions. We predicted the fold group (ordered or disordered) of proteins in the network from their primary sequences. The network analysis indicated that protein disorder has a positive effect on the connectivity of proteins in the network, but do not fully explains the interactivity.</p> <p>Conclusions</p> <p>The approach opens a perspective to study effects of biological properties of individual entities on the structure of biological networks.</p>
url http://www.biomedcentral.com/1471-2105/11/46
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