Evidence map›Paper›PMID 24286232›Full record

ArticleBMC bioinformatics2013

Partial inhibition and bilevel optimization in flux balance analysis.

Giuseppe Facchetti, Claudio Altafini

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Article in BMC bioinformatics, 2013. 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
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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Giuseppe FacchettiSISSA (International School for Advanced Studies) Functional Analysis Dept, - Via Bonomea 265 - 34136, Trieste, Italy. altafini@sissa.it.
Claudio Altafini

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationWithin 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.

resultsIn 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.

conclusionsThe 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.

Indexed as

Aldose-Ketose IsomerasesAlgorithmsComputer SimulationDrug CombinationsDrug InteractionsEscherichia coliGlutamate DehydrogenaseHumansMetabolic EngineeringMetabolic Flux AnalysisNeural Networks, ComputerSoftwareSupport Vector MachineTransketolaseAldose-Ketose IsomerasesDrug CombinationsGlutamate Dehydrogenaseribosephosphate isomeraseTransketolase

Identifiers

PMID24286232
PMCPMC4219332

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