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dc.contributor.author
Noor, Elad
dc.contributor.author
Flamholz, Avi, I
dc.contributor.author
Bar-Even, Arren
dc.contributor.author
Davidi, Dan
dc.contributor.author
Milo, Ron
dc.contributor.author
Liebermeister, Wolfram
dc.date.accessioned
2018-12-13T13:45:32Z
dc.date.available
2017-06-12T17:05:38Z
dc.date.available
2018-12-13T13:45:32Z
dc.date.issued
2016-11-03
dc.identifier.issn
1553-734X
dc.identifier.issn
1553-7358
dc.identifier.other
10.1371/journal.pcbi.1005167
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/123705
dc.identifier.doi
10.3929/ethz-b-000123705
dc.description.abstract
Bacterial growth depends crucially on metabolic fluxes, which are limited by the cell’s capacity to maintain metabolic enzymes. The necessary enzyme amount per unit flux is a major determinant of metabolic strategies both in evolution and bioengineering. It depends on enzyme parameters (such as kcat and KM constants), but also on metabolite concentrations. Moreover, similar amounts of different enzymes might incur different costs for the cell, depending on enzyme-specific properties such as protein size and half-life. Here, we developed enzyme cost minimization (ECM), a scalable method for computing enzyme amounts that support a given metabolic flux at a minimal protein cost. The complex interplay of enzyme and metabolite concentrations, e.g. through thermodynamic driving forces and enzyme saturation, would make it hard to solve this optimization problem directly. By treating enzyme cost as a function of metabolite levels, we formulated ECM as a numerically tractable, convex optimization problem. Its tiered approach allows for building models at different levels of detail, depending on the amount of available data. Validating our method with measured metabolite and protein levels in E. coli central metabolism, we found typical prediction fold errors of 4.1 and 2.6, respectively, for the two kinds of data. This result from the cost-optimized metabolic state is significantly better than randomly sampled metabolite profiles, supporting the hypothesis that enzyme cost is important for the fitness of E. coli. ECM can be used to predict enzyme levels and protein cost in natural and engineered pathways, and could be a valuable computational tool to assist metabolic engineering projects. Furthermore, it establishes a direct connection between protein cost and thermodynamics, and provides a physically plausible and computationally tractable way to include enzyme kinetics into constraint-based metabolic models, where kinetics have usually been ignored or oversimplified.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
PLOS
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.title
The Protein Cost of Metabolic Fluxes: Prediction from Enzymatic Rate Laws and Cost Minimization
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
ethz.journal.title
PLoS Computational Biology
ethz.journal.volume
12
en_US
ethz.journal.issue
11
en_US
ethz.journal.abbreviated
PLOS comput. biol.
ethz.pages.start
e1005167
en_US
ethz.size
29 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
San Francisco, CA
ethz.publication.status
published
en_US
ethz.date.deposited
2017-06-12T17:05:57Z
ethz.source
ECIT
ethz.identifier.importid
imp593654f0c44c619253
ethz.ecitpid
pub:186134
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2017-07-12T16:07:52Z
ethz.rosetta.lastUpdated
2024-02-02T06:49:22Z
ethz.rosetta.versionExported
true
ethz.COinS
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