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Domain-specific model selection for structural identification of the Rab5-Rab7 dynamics in endocytosis.

Tanevski J, Todorovski L, Kalaidzidis Y, Džeroski S - BMC Syst Biol (2015)

Bottom Line: Furthermore, taking into account the complexity of the model does not lead to better model selection.However, the use of domain-specific criteria results in a remarkable improvement over the other two model selection criteria.We also find that some of the model structures discarded as implausible in previous studies lead to the expected Rab5-Rab7 switch behavior.

View Article: PubMed Central - PubMed

Affiliation: Jožef Stefan Institute, Jamova cesta 39, Ljubljana, 1000, Slovenia. jovan.tanevski@ijs.si.

ABSTRACT

Background: Given its recent rapid development and the central role that modeling plays in the discipline, systems biology clearly needs methods for automated modeling of dynamical systems. Process-based modeling focuses on explanatory models of dynamical systems; it constructs such models from measured time-course data and formalized modeling knowledge. In this paper, we apply process-based modeling to the practically relevant task of modeling the Rab5-Rab7 conversion switch in endocytosis. The task is difficult due to the limited observability of the system variables and the noisy measurements, which pose serious challenges to the process of model selection. To address these issues, we propose a domain-specific model selection criteria that take into account knowledge about the necessary properties of the simulated model behavior.

Results: In a series of modeling experiments, we compare the results of process-based modeling obtained with different model selection criteria. The first is the standard maximum likelihood criterion based solely on least-squares model error. The second one is a parsimony-based criterion that also takes into account model complexity. We also introduce three domain-specific criteria based on domain expert expectations about the simulated behavior of an endocytosis model. According to the first criterion, 90 of the candidate models are indistinguishable. Furthermore, taking into account the complexity of the model does not lead to better model selection. However, the use of domain-specific criteria results in a remarkable improvement over the other two model selection criteria.

Conclusions: We demonstrate the applicability of process-based modeling to the task of modeling the Rab5-Rab7 dynamics in endocytosis. Our experiments show that the domain-specific criteria outperform the standard domain-independent criteria for model selection. We also find that some of the model structures discarded as implausible in previous studies lead to the expected Rab5-Rab7 switch behavior.

No MeSH data available.


A graphical representation of the Rab5-Rab7 interaction model structure as considered by del Conte-Zerial et al. [15]
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Fig2: A graphical representation of the Rab5-Rab7 interaction model structure as considered by del Conte-Zerial et al. [15]

Mentions: Figure 2 provides a graphical representation of the model structure [15], where the dashed lines represent optional interactions between the Rab5 and Rab7 protein domains, while the solid lines represent non-optional (mandatory) interactions. The pointed arrows represent the catalisation (activation) of the corresponding exchange or hydrolysis, while the inhibition of the GDP/GTP exchange by the GEF5Exchange Inhibitor is represented by a truncated line. del Conte-Zerial et al. [15] consider a different set of functional forms for modeling each of the four (GEF and GAP) interactions; the combinations of the different functional forms they consider result in only 54 different model structures from the possible 126.Fig. 2


Domain-specific model selection for structural identification of the Rab5-Rab7 dynamics in endocytosis.

Tanevski J, Todorovski L, Kalaidzidis Y, Džeroski S - BMC Syst Biol (2015)

A graphical representation of the Rab5-Rab7 interaction model structure as considered by del Conte-Zerial et al. [15]
© Copyright Policy - open-access
Related In: Results  -  Collection

License 1 - License 2
Show All Figures
getmorefigures.php?uid=PMC4482292&req=5

Fig2: A graphical representation of the Rab5-Rab7 interaction model structure as considered by del Conte-Zerial et al. [15]
Mentions: Figure 2 provides a graphical representation of the model structure [15], where the dashed lines represent optional interactions between the Rab5 and Rab7 protein domains, while the solid lines represent non-optional (mandatory) interactions. The pointed arrows represent the catalisation (activation) of the corresponding exchange or hydrolysis, while the inhibition of the GDP/GTP exchange by the GEF5Exchange Inhibitor is represented by a truncated line. del Conte-Zerial et al. [15] consider a different set of functional forms for modeling each of the four (GEF and GAP) interactions; the combinations of the different functional forms they consider result in only 54 different model structures from the possible 126.Fig. 2

Bottom Line: Furthermore, taking into account the complexity of the model does not lead to better model selection.However, the use of domain-specific criteria results in a remarkable improvement over the other two model selection criteria.We also find that some of the model structures discarded as implausible in previous studies lead to the expected Rab5-Rab7 switch behavior.

View Article: PubMed Central - PubMed

Affiliation: Jožef Stefan Institute, Jamova cesta 39, Ljubljana, 1000, Slovenia. jovan.tanevski@ijs.si.

ABSTRACT

Background: Given its recent rapid development and the central role that modeling plays in the discipline, systems biology clearly needs methods for automated modeling of dynamical systems. Process-based modeling focuses on explanatory models of dynamical systems; it constructs such models from measured time-course data and formalized modeling knowledge. In this paper, we apply process-based modeling to the practically relevant task of modeling the Rab5-Rab7 conversion switch in endocytosis. The task is difficult due to the limited observability of the system variables and the noisy measurements, which pose serious challenges to the process of model selection. To address these issues, we propose a domain-specific model selection criteria that take into account knowledge about the necessary properties of the simulated model behavior.

Results: In a series of modeling experiments, we compare the results of process-based modeling obtained with different model selection criteria. The first is the standard maximum likelihood criterion based solely on least-squares model error. The second one is a parsimony-based criterion that also takes into account model complexity. We also introduce three domain-specific criteria based on domain expert expectations about the simulated behavior of an endocytosis model. According to the first criterion, 90 of the candidate models are indistinguishable. Furthermore, taking into account the complexity of the model does not lead to better model selection. However, the use of domain-specific criteria results in a remarkable improvement over the other two model selection criteria.

Conclusions: We demonstrate the applicability of process-based modeling to the task of modeling the Rab5-Rab7 dynamics in endocytosis. Our experiments show that the domain-specific criteria outperform the standard domain-independent criteria for model selection. We also find that some of the model structures discarded as implausible in previous studies lead to the expected Rab5-Rab7 switch behavior.

No MeSH data available.