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MCS(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks
MOTIVATION: Constraint-based modeling of metabolic networks helps researchers gain insight into the metabolic processes of many organisms, both prokaryotic and eukaryotic. Minimal cut sets (MCSs) are minimal sets of reactions whose inhibition blocks a target reaction in a metabolic network. Most app...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612898/ https://www.ncbi.nlm.nih.gov/pubmed/31510702 http://dx.doi.org/10.1093/bioinformatics/btz393 |
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author | Miraskarshahi, Reza Zabeti, Hooman Stephen, Tamon Chindelevitch, Leonid |
author_facet | Miraskarshahi, Reza Zabeti, Hooman Stephen, Tamon Chindelevitch, Leonid |
author_sort | Miraskarshahi, Reza |
collection | PubMed |
description | MOTIVATION: Constraint-based modeling of metabolic networks helps researchers gain insight into the metabolic processes of many organisms, both prokaryotic and eukaryotic. Minimal cut sets (MCSs) are minimal sets of reactions whose inhibition blocks a target reaction in a metabolic network. Most approaches for finding the MCSs in constrained-based models require, either as an intermediate step or as a byproduct of the calculation, the computation of the set of elementary flux modes (EFMs), a convex basis for the valid flux vectors in the network. Recently, Ballerstein et al. proposed a method for computing the MCSs of a network without first computing its EFMs, by creating a dual network whose EFMs are a superset of the MCSs of the original network. However, their dual network is always larger than the original network and depends on the target reaction. Here we propose the construction of a different dual network, which is typically smaller than the original network and is independent of the target reaction, for the same purpose. We prove the correctness of our approach, minimal coordinated support (MCS(2)), and describe how it can be modified to compute the few smallest MCSs for a given target reaction. RESULTS: We compare MCS(2) to the method of Ballerstein et al. and two other existing methods. We show that MCS(2) succeeds in calculating the full set of MCSs in many models where other approaches cannot finish within a reasonable amount of time. Thus, in addition to its theoretical novelty, our approach provides a practical advantage over existing methods. AVAILABILITY AND IMPLEMENTATION: MCS(2) is freely available at https://github.com/RezaMash/MCS under the GNU 3.0 license. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6612898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66128982019-07-12 MCS(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks Miraskarshahi, Reza Zabeti, Hooman Stephen, Tamon Chindelevitch, Leonid Bioinformatics Ismb/Eccb 2019 Conference Proceedings MOTIVATION: Constraint-based modeling of metabolic networks helps researchers gain insight into the metabolic processes of many organisms, both prokaryotic and eukaryotic. Minimal cut sets (MCSs) are minimal sets of reactions whose inhibition blocks a target reaction in a metabolic network. Most approaches for finding the MCSs in constrained-based models require, either as an intermediate step or as a byproduct of the calculation, the computation of the set of elementary flux modes (EFMs), a convex basis for the valid flux vectors in the network. Recently, Ballerstein et al. proposed a method for computing the MCSs of a network without first computing its EFMs, by creating a dual network whose EFMs are a superset of the MCSs of the original network. However, their dual network is always larger than the original network and depends on the target reaction. Here we propose the construction of a different dual network, which is typically smaller than the original network and is independent of the target reaction, for the same purpose. We prove the correctness of our approach, minimal coordinated support (MCS(2)), and describe how it can be modified to compute the few smallest MCSs for a given target reaction. RESULTS: We compare MCS(2) to the method of Ballerstein et al. and two other existing methods. We show that MCS(2) succeeds in calculating the full set of MCSs in many models where other approaches cannot finish within a reasonable amount of time. Thus, in addition to its theoretical novelty, our approach provides a practical advantage over existing methods. AVAILABILITY AND IMPLEMENTATION: MCS(2) is freely available at https://github.com/RezaMash/MCS under the GNU 3.0 license. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-07 2019-07-05 /pmc/articles/PMC6612898/ /pubmed/31510702 http://dx.doi.org/10.1093/bioinformatics/btz393 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Ismb/Eccb 2019 Conference Proceedings Miraskarshahi, Reza Zabeti, Hooman Stephen, Tamon Chindelevitch, Leonid MCS(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks |
title | MCS(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks |
title_full | MCS(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks |
title_fullStr | MCS(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks |
title_full_unstemmed | MCS(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks |
title_short | MCS(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks |
title_sort | mcs(2): minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks |
topic | Ismb/Eccb 2019 Conference Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612898/ https://www.ncbi.nlm.nih.gov/pubmed/31510702 http://dx.doi.org/10.1093/bioinformatics/btz393 |
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