Modeling Integrated Cellular Machinery Using Hybrid Petri-Boolean Networks

dc.citation.firstpagee1003306
dc.citation.issueNumber11
dc.citation.journalTitlePLoS Computational Biology
dc.citation.volumeNumber9
dc.contributor.authorBerestovsky, Natalie
dc.contributor.authorZhou, Wanding
dc.contributor.authorNagrath, Deepak
dc.contributor.authorNakhleh, Luay
dc.date.accessioned2013-11-21T19:44:19Z
dc.date.available2013-11-21T19:44:19Z
dc.date.issued2013
dc.description.abstractThe behavior and phenotypic changes of cells are governed by a cellular circuitry that represents a set of biochemical reactions. Based on biological functions, this circuitry is divided into three types of networks, each encoding for a major biological process: signal transduction, transcription regulation, and metabolism. This division has generally enabled taming computational complexity dealing with the entire system, allowed for using modeling techniques that are specific to each of the components, and achieved separation of the different time scales at which reactions in each of the three networks occur. Nonetheless, with this division comes loss of information and power needed to elucidate certain cellular phenomena. Within the cell, these three types of networks work in tandem, and each produces signals and/or substances that are used by the others to process information and operate normally. Therefore, computational techniques for modeling integrated cellular machinery are needed. In this work, we propose an integrated hybrid model (IHM) that combines Petri nets and Boolean networks to model integrated cellular networks. Coupled with a stochastic simulation mechanism, the model simulates the dynamics of the integrated network, and can be perturbed to generate testable hypotheses. Our model is qualitative and is mostly built upon knowledge from the literature and requires fine-tuning of very few parameters. We validated our model on two systems: the transcriptional regulation of glucose metabolism in human cells, and cellular osmoregulation in S. cerevisiae. The model produced results that are in very good agreement with experimental data, and produces valid hypotheses. The abstract nature of our model and the ease of its construction makes it a very good candidate for modeling integrated networks from qualitative data. The results it produces can guide the practitioner to zoom into components and interconnections and investigate them using such more detailed mathematical models.
dc.identifier.citationBerestovsky, Natalie, Zhou, Wanding, Nagrath, Deepak, et al.. "Modeling Integrated Cellular Machinery Using Hybrid Petri-Boolean Networks." <i>PLoS Computational Biology,</i> 9, no. 11 (2013) Public Library of Science: e1003306. http://dx.doi.org/10.1371/journal.pcbi.1003306.
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pcbi.1003306
dc.identifier.urihttps://hdl.handle.net/1911/75181
dc.language.isoeng
dc.publisherPublic Library of Science
dc.rightsThis is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0
dc.titleModeling Integrated Cellular Machinery Using Hybrid Petri-Boolean Networks
dc.typeJournal article
dc.type.dcmiText
dc.type.publicationpublisher version
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