Evidence map›Paper›PMID 25323319›Full record

ArticleJournal of mathematical biology2015

On dynamically generating relevant elementary flux modes in a metabolic network using optimization.

Hildur Æsa Oddsdóttir, Erika Hagrot, Véronique Chotteau, Anders Forsgren

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Article in Journal of mathematical biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hildur Æsa OddsdóttirDepartment of Mathematics, Optimization and Systems Theory, KTH Royal Institute of Technology, SE-100 44, Stockholm, Sweden, haodd@kth.se.
Erika Hagrot
Véronique Chotteau
Anders Forsgren

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elementary flux modes (EFMs) are pathways through a metabolic reaction network that connect external substrates to products. Using EFMs, a metabolic network can be transformed into its macroscopic counterpart, in which the internal metabolites have been eliminated and only external metabolites remain. In EFMs-based metabolic flux analysis (MFA) experimentally determined external fluxes are used to estimate the flux of each EFM. It is in general prohibitive to enumerate all EFMs for complex networks, since the number of EFMs increases rapidly with network complexity. In this work we present an optimization-based method that dynamically generates a subset of EFMs and solves the EFMs-based MFA problem simultaneously. The obtained subset contains EFMs that contribute to the optimal solution of the EFMs-based MFA problem. The usefulness of our method was examined in a case-study using data from a Chinese hamster ovary cell culture and two networks of varied complexity. It was demonstrated that the EFMs-based MFA problem could be solved at a low computational cost, even for the more complex network. Additionally, only a fraction of the total number of EFMs was needed to compute the optimal solution.

Indexed as

Metabolic Networks and PathwaysModels, BiologicalAlgorithmsAnimalsCHO CellsComputer SimulationCricetinaeCricetulusMathematical ConceptsMetabolic Flux Analysis

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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.