Evidence map›Paper›PMID 30066662›Full record

ArticleBMC bioinformatics2018

Emerging ensembles of kinetic parameters to characterize observed metabolic phenotypes.

Riccardo Colombo, Chiara Damiani, David Gilbert, Monika Heiner, Giancarlo Mauri, Dario Pescini

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Construction and Analysis of Human Diseases and Metabolites Network.Frontiers in bioengineering and biotechnology · 2020
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Riccardo ColomboDepartment of Informatics, Systems and Communication, University of Milan - Bicocca, Viale Sarca, 336, Milan, 20126, Italy. riccardo.colombo@disco.unimib.it.
Chiara DamianiDepartment of Informatics, Systems and Communication, University of Milan - Bicocca, Viale Sarca, 336, Milan, 20126, Italy.
David GilbertCollege of Engineering, Design and Physical Sciences, Brunel University, Middlesex, London, Uxbridg, UB8 3PH, UK.
Monika HeinerComputer Science Department, Brandenburg University of Technology Cottbus-Senftenberg, Walther-Pauer-Str. 2, Cottbus, D-03046, Germany.
Giancarlo MauriDepartment of Informatics, Systems and Communication, University of Milan - Bicocca, Viale Sarca, 336, Milan, 20126, Italy.
Dario PesciniSYSBIO - Centre of Systems Biology, Piazza della Scienza, 2, Milan, 20126, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDetermining the value of kinetic constants for a metabolic system in the exact physiological conditions is an extremely hard task. However, this kind of information is of pivotal relevance to effectively simulate a biological phenomenon as complex as metabolism.

resultsTo overcome this issue, we propose to investigate emerging properties of ensembles of sets of kinetic constants leading to the biological readout observed in different experimental conditions. To this aim, we exploit information retrievable from constraint-based analyses (i.e. metabolic flux distributions at steady state) with the goal to generate feasible values for kinetic constants exploiting the mass action law. The sets retrieved from the previous step will be used to parametrize a mechanistic model whose simulation will be performed to reconstruct the dynamics of the system (until reaching the metabolic steady state) for each experimental condition. Every parametrization that is in accordance with the expected metabolic phenotype is collected in an ensemble whose features are analyzed to determine the emergence of properties of a phenotype. In this work we apply the proposed approach to identify ensembles of kinetic parameters for five metabolic phenotypes of E. Coli, by analyzing five different experimental conditions associated with the ECC2comp model recently published by Hädicke and collaborators.

conclusionsOur results suggest that the parameter values of just few reactions are responsible for the emergence of a metabolic phenotype. Notably, in contrast with constraint-based approaches such as Flux Balance Analysis, the methodology used in this paper does not require to assume that metabolism is optimizing towards a specific goal.

Indexed as

Metabolic Networks and PathwaysBiomassComputer SimulationEscherichia coliEscherichia coli ProteinsKineticsPhenotypeTime FactorsEscherichia coli ProteinsEnsemblesFluxesKinetic parametersMechanistic simulationsMetabolismODEsSteady stateSystems biology

Identifiers

PMID30066662
PMCPMC6201900

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.