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dc.contributor.author
Mayorga, Luis Segundo  
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Cebrián, José Ignacio  
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Verma, Meghna  
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Hoops, Stefan  
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Bassaganya-Riera, Josep  
dc.date.available
2020-01-09T15:23:48Z  
dc.date.issued
2018-11  
dc.identifier.citation
Mayorga, Luis Segundo; Cebrián, José Ignacio; Verma, Meghna; Hoops, Stefan; Bassaganya-Riera, Josep; Reconstruction of endosomal organization and function by a combination of ODE and agent-based modeling strategies; BioMed Central; Biology Direct; 13; 1; 11-2018; 1-21  
dc.identifier.issn
1745-6150  
dc.identifier.uri
http://hdl.handle.net/11336/94123  
dc.description.abstract
Background: Reproducing cell processes using an in silico system is an essential tool for understanding the underlying mechanisms and emergent properties of this extraordinary complex biological machine. However, computational models are seldom applied in the field of intracellular trafficking. In a cell, numerous molecular interactions occur on the surface or in the interior of membrane-bound compartments that continually change position and undergo dynamic processes of fusion and fission. At present, the available simulation tools are not suitable to develop models that incorporate the dynamic evolution of the cell organelles. Results: We developed a modeling platform combining Repast (Agent-Based Modeling, ABM) and COPASI (Differential Equations, ODE) that can be used to reproduce complex networks of molecular interactions. These interactions occur in dynamic cell organelles that change position and composition over the course of time. These two modeling strategies are fundamentally different and comprise of complementary capabilities. The ODEs can easily model the networks of molecular interactions, signaling cascades, and complex metabolic reactions. On the other hand, ABM software is especially suited to simulate the movement, interaction, fusion, and fission of dynamic organelles. We used the combined ABM-ODE platform to simulate the transport of soluble and membrane-associated cargoes that move along an endocytic route composed of early, sorting, recycling and late endosomes. We showed that complex processes that strongly depend on transport can be modeled. As an example, the hydrolysis of a GM2-like glycolipid was programmed by adding a trans-Golgi network compartment, lysosomal enzyme trafficking, endosomal acidification, and cholesterol processing to the simulation model. Conclusions: The model captures the highly dynamic nature of cell compartments that fuse and divide, creating different conditions for each organelle. We expect that this modeling strategy will be useful to understand the logic underlying the organization and function of the endomembrane system. Reviewers: This article was reviewed by Drs. Rafael Fernández-Chacón, James Faeder, and Thomas Simmen.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
BioMed Central  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
AGENT-BASED MODELING  
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DIFFERENTIAL EQUATION MODELING  
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ENDOCYTIC PATHWAY  
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INTRACELLULAR TRANSPORT  
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LIPID METABOLISM  
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RAB DOMAINS  
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Otras Ciencias de la Computación e Información  
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Ciencias de la Computación e Información  
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CIENCIAS NATURALES Y EXACTAS  
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Bioquímica y Biología Molecular  
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Ciencias Biológicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Reconstruction of endosomal organization and function by a combination of ODE and agent-based modeling strategies  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-10-23T19:30:22Z  
dc.journal.volume
13  
dc.journal.number
1  
dc.journal.pagination
1-21  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Mayorga, Luis Segundo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina  
dc.description.fil
Fil: Cebrián, José Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina  
dc.description.fil
Fil: Verma, Meghna. Biocomplexity Institute; Estados Unidos. Virginia Polytechnic Institute And State University;  
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Fil: Hoops, Stefan. University of Virginia; Estados Unidos. Biocomplexity Institute; Estados Unidos  
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Fil: Bassaganya-Riera, Josep. Biocomplexity Institute; Estados Unidos  
dc.journal.title
Biology Direct  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1186/s13062-018-0227-4  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://biologydirect.biomedcentral.com/articles/10.1186/s13062-018-0227-4