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  4. Optimization of [superscript 13]C isotopic tracers for metabolic flux analysis in mammalian cells

Optimization of [superscript 13]C isotopic tracers for metabolic flux analysis in mammalian cells

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Author(s)
Walther, Jason L.
•
Metallo, Christian M.
•
Zhang, Jie
•
Stephanopoulos, Gregory
Date Issued
December 2011
Journal
Metabolic Engineering
Publisher
Elsevier
Citation
Walther, Jason L., Christian M. Metallo, Jie Zhang, and Gregory Stephanopoulos. “Optimization of [superscript 13]C Isotopic Tracers for Metabolic Flux Analysis in Mammalian Cells.” Metabolic Engineering 14, no. 2 (March 2012): 162–171.
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Author's final manuscript
Abstract
Mammalian cells consume and metabolize various substrates from their surroundings for energy generation and biomass synthesis. Glucose and glutamine, in particular, are the primary carbon sources for proliferating cancer cells. While this combination of substrates generates static labeling patterns for use in [superscript 13]C metabolic flux analysis (MFA), the inability of single tracers to effectively label all pathways poses an obstacle for comprehensive flux determination within a given experiment. To address this issue we applied a genetic algorithm to optimize mixtures of [superscript 13]C-labeled glucose and glutamine for use in MFA. We identified tracer combinations that minimized confidence intervals in an experimentally determined flux network describing central carbon metabolism in tumor cells. Additional simulations were used to determine the robustness of the [1,2-[superscript 13]C[subscript 2]]glucose/[U-[superscript 13]C[subscript 5]]glutamine tracer combination with respect to perturbations in the network. Finally, we experimentally validated the improved performance of this tracer set relative to glucose tracers alone in a cancer cell line. This versatile method allows researchers to determine the optimal tracer combination to use for a specific metabolic network, and our findings applied to cancer cells significantly enhance the ability of MFA experiments to precisely quantify fluxes in higher organisms.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
Terms of Use
Creative Commons Attribution-Noncommercial-NoDerivatives
http://creativecommons.org/licenses/by-nc-nd/4.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/99396
DOI of Published Version
https://doi.org/10.1016/j.ymben.2011.12.004
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