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Partial inhibition and bilevel optimization in flux balance analysis
MOTIVATION: Within Flux Balance Analysis, the investigation of complex subtasks, such as finding the optimal perturbation of the network or finding an optimal combination of drugs, often requires to set up a bilevel optimization problem. In order to keep the linearity and convexity of these nested o...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219332/ https://www.ncbi.nlm.nih.gov/pubmed/24286232 http://dx.doi.org/10.1186/1471-2105-14-344 |
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author | Facchetti, Giuseppe Altafini, Claudio |
author_facet | Facchetti, Giuseppe Altafini, Claudio |
author_sort | Facchetti, Giuseppe |
collection | PubMed |
description | MOTIVATION: Within Flux Balance Analysis, the investigation of complex subtasks, such as finding the optimal perturbation of the network or finding an optimal combination of drugs, often requires to set up a bilevel optimization problem. In order to keep the linearity and convexity of these nested optimization problems, an ON/OFF description of the effect of the perturbation (i.e. Boolean variable) is normally used. This restriction may not be realistic when one wants, for instance, to describe the partial inhibition of a reaction induced by a drug. RESULTS: In this paper we present a formulation of the bilevel optimization which overcomes the oversimplified ON/OFF modeling while preserving the linear nature of the problem. A case study is considered: the search of the best multi-drug treatment which modulates an objective reaction and has the minimal perturbation on the whole network. The drug inhibition is described and modulated through a convex combination of a fixed number of Boolean variables. The results obtained from the application of the algorithm to the core metabolism of E.coli highlight the possibility of finding a broader spectrum of drug combinations compared to a simple ON/OFF modeling. CONCLUSIONS: The method we have presented is capable of treating partial inhibition inside a bilevel optimization, without loosing the linearity property, and with reasonable computational performances also on large metabolic networks. The more fine-graded representation of the perturbation allows to enlarge the repertoire of synergistic combination of drugs for tasks such as selective perturbation of cellular metabolism. This may encourage the use of the approach also for other cases in which a more realistic modeling is required. |
format | Online Article Text |
id | pubmed-4219332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42193322014-11-07 Partial inhibition and bilevel optimization in flux balance analysis Facchetti, Giuseppe Altafini, Claudio BMC Bioinformatics Research Article MOTIVATION: Within Flux Balance Analysis, the investigation of complex subtasks, such as finding the optimal perturbation of the network or finding an optimal combination of drugs, often requires to set up a bilevel optimization problem. In order to keep the linearity and convexity of these nested optimization problems, an ON/OFF description of the effect of the perturbation (i.e. Boolean variable) is normally used. This restriction may not be realistic when one wants, for instance, to describe the partial inhibition of a reaction induced by a drug. RESULTS: In this paper we present a formulation of the bilevel optimization which overcomes the oversimplified ON/OFF modeling while preserving the linear nature of the problem. A case study is considered: the search of the best multi-drug treatment which modulates an objective reaction and has the minimal perturbation on the whole network. The drug inhibition is described and modulated through a convex combination of a fixed number of Boolean variables. The results obtained from the application of the algorithm to the core metabolism of E.coli highlight the possibility of finding a broader spectrum of drug combinations compared to a simple ON/OFF modeling. CONCLUSIONS: The method we have presented is capable of treating partial inhibition inside a bilevel optimization, without loosing the linearity property, and with reasonable computational performances also on large metabolic networks. The more fine-graded representation of the perturbation allows to enlarge the repertoire of synergistic combination of drugs for tasks such as selective perturbation of cellular metabolism. This may encourage the use of the approach also for other cases in which a more realistic modeling is required. BioMed Central 2013-11-29 /pmc/articles/PMC4219332/ /pubmed/24286232 http://dx.doi.org/10.1186/1471-2105-14-344 Text en Copyright © 2013 Facchetti and Altafini; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Facchetti, Giuseppe Altafini, Claudio Partial inhibition and bilevel optimization in flux balance analysis |
title | Partial inhibition and bilevel optimization in flux balance analysis |
title_full | Partial inhibition and bilevel optimization in flux balance analysis |
title_fullStr | Partial inhibition and bilevel optimization in flux balance analysis |
title_full_unstemmed | Partial inhibition and bilevel optimization in flux balance analysis |
title_short | Partial inhibition and bilevel optimization in flux balance analysis |
title_sort | partial inhibition and bilevel optimization in flux balance analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219332/ https://www.ncbi.nlm.nih.gov/pubmed/24286232 http://dx.doi.org/10.1186/1471-2105-14-344 |
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