Literature DB >> 28793222

Thermodynamic Constraints Improve Metabolic Networks.

Elias W Krumholz1, Igor G L Libourel2.   

Abstract

In pursuit of establishing a realistic metabolic phenotypic space, the reversibility of reactions is thermodynamically constrained in modern metabolic networks. The reversibility constraints follow from heuristic thermodynamic poise approximations that take anticipated cellular metabolite concentration ranges into account. Because constraints reduce the feasible space, draft metabolic network reconstructions may need more extensive reconciliation, and a larger number of genes may become essential. Notwithstanding ubiquitous application, the effect of reversibility constraints on the predictive capabilities of metabolic networks has not been investigated in detail. Instead, work has focused on the implementation and validation of the thermodynamic poise calculation itself. With the advance of fast linear programming-based network reconciliation, the effects of reversibility constraints on network reconciliation and gene essentiality predictions have become feasible and are the subject of this study. Networks with thermodynamically informed reversibility constraints outperformed gene essentiality predictions compared to networks that were constrained with randomly shuffled constraints. Unconstrained networks predicted gene essentiality as accurately as thermodynamically constrained networks, but predicted substantially fewer essential genes. Networks that were reconciled with sequence similarity data and strongly enforced reversibility constraints outperformed all other networks. We conclude that metabolic network analysis confirmed the validity of the thermodynamic constraints, and that thermodynamic poise information is actionable during network reconciliation.
Copyright © 2017 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Mesh:

Year:  2017        PMID: 28793222      PMCID: PMC5549646          DOI: 10.1016/j.bpj.2017.06.018

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  65 in total

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Review 2.  Construction of Multiscale Genome-Scale Metabolic Models: Frameworks and Challenges.

Authors:  Xinyu Bi; Yanfeng Liu; Jianghua Li; Guocheng Du; Xueqin Lv; Long Liu
Journal:  Biomolecules       Date:  2022-05-19

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  4 in total

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