A roadmap for interpreting 13C metabolite labeling patterns from cells

Measuring intracellular metabolism has increasingly led to important insights in biomedical research. [superscript 13]C tracer analysis, although less information-rich than quantitative [superscript 13]C flux analysis that requires computational data integration, has been established as a time-effic...

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Main Author: Stephanopoulos, Gregory
Other Authors: Massachusetts Institute of Technology. Department of Chemical Engineering
Format: Article
Language:en_US
Published: Elsevier 2017
Online Access:http://hdl.handle.net/1721.1/107921
https://orcid.org/0000-0001-6909-4568
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author Stephanopoulos, Gregory
author2 Massachusetts Institute of Technology. Department of Chemical Engineering
author_facet Massachusetts Institute of Technology. Department of Chemical Engineering
Stephanopoulos, Gregory
author_sort Stephanopoulos, Gregory
collection MIT
description Measuring intracellular metabolism has increasingly led to important insights in biomedical research. [superscript 13]C tracer analysis, although less information-rich than quantitative [superscript 13]C flux analysis that requires computational data integration, has been established as a time-efficient method to unravel relative pathway activities, qualitative changes in pathway contributions, and nutrientcontributions. Here, we review selected key issues in interpreting [superscript 13]C metabolite labeling patterns, with the goal of drawing accurate conclusions from steady state and dynamic stable isotopic tracer experiments
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spelling mit-1721.1/1079212022-09-27T22:49:09Z A roadmap for interpreting 13C metabolite labeling patterns from cells Stephanopoulos, Gregory Massachusetts Institute of Technology. Department of Chemical Engineering Stephanopoulos, Gregory Measuring intracellular metabolism has increasingly led to important insights in biomedical research. [superscript 13]C tracer analysis, although less information-rich than quantitative [superscript 13]C flux analysis that requires computational data integration, has been established as a time-efficient method to unravel relative pathway activities, qualitative changes in pathway contributions, and nutrientcontributions. Here, we review selected key issues in interpreting [superscript 13]C metabolite labeling patterns, with the goal of drawing accurate conclusions from steady state and dynamic stable isotopic tracer experiments 2017-04-06T20:35:01Z 2017-04-06T20:35:01Z 2015-08 2015-08 Article http://purl.org/eprint/type/JournalArticle 09581669 http://hdl.handle.net/1721.1/107921 Buescher, Joerg M et al. “A Roadmap for Interpreting 13C Metabolite Labeling Patterns from Cells.” Current Opinion in Biotechnology 34 (2015): 189–201. https://orcid.org/0000-0001-6909-4568 en_US http://dx.doi.org/10.1016/j.copbio.2015.02.003 Current Opinion in Biotechnology Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Elsevier PMC
spellingShingle Stephanopoulos, Gregory
A roadmap for interpreting 13C metabolite labeling patterns from cells
title A roadmap for interpreting 13C metabolite labeling patterns from cells
title_full A roadmap for interpreting 13C metabolite labeling patterns from cells
title_fullStr A roadmap for interpreting 13C metabolite labeling patterns from cells
title_full_unstemmed A roadmap for interpreting 13C metabolite labeling patterns from cells
title_short A roadmap for interpreting 13C metabolite labeling patterns from cells
title_sort roadmap for interpreting 13c metabolite labeling patterns from cells
url http://hdl.handle.net/1721.1/107921
https://orcid.org/0000-0001-6909-4568
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