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(13)C labeling experiments at metabolic nonstationary conditions: An exploratory study
BACKGROUND: Stimulus Response Experiments to unravel the regulatory properties of metabolic networks are becoming more and more popular. However, their ability to determine enzyme kinetic parameters has proven to be limited with the presently available data. In metabolic flux analysis, the use of (1...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2373788/ https://www.ncbi.nlm.nih.gov/pubmed/18366666 http://dx.doi.org/10.1186/1471-2105-9-152 |
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author | Wahl, Sebastian Aljoscha Nöh, Katharina Wiechert, Wolfgang |
author_facet | Wahl, Sebastian Aljoscha Nöh, Katharina Wiechert, Wolfgang |
author_sort | Wahl, Sebastian Aljoscha |
collection | PubMed |
description | BACKGROUND: Stimulus Response Experiments to unravel the regulatory properties of metabolic networks are becoming more and more popular. However, their ability to determine enzyme kinetic parameters has proven to be limited with the presently available data. In metabolic flux analysis, the use of (13)C labeled substrates together with isotopomer modeling solved the problem of underdetermined networks and increased the accuracy of flux estimations significantly. RESULTS: In this contribution, the idea of increasing the information content of the dynamic experiment by adding (13)C labeling is analyzed. For this purpose a small example network is studied by simulation and statistical methods. Different scenarios regarding available measurements are analyzed and compared to a non-labeled reference experiment. Sensitivity analysis revealed a specific influence of the kinetic parameters on the labeling measurements. Statistical methods based on parameter sensitivities and different measurement models are applied to assess the information gain of the labeled stimulus response experiment. CONCLUSION: It was found that the use of a (specifically) labeled substrate will significantly increase the parameter estimation accuracy. An overall information gain of about a factor of six is observed for the example network. The information gain is achieved from the specific influence of the kinetic parameters towards the labeling measurements. This also leads to a significant decrease in correlation of the kinetic parameters compared to an experiment without (13)C-labeled substrate. |
format | Text |
id | pubmed-2373788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23737882008-05-12 (13)C labeling experiments at metabolic nonstationary conditions: An exploratory study Wahl, Sebastian Aljoscha Nöh, Katharina Wiechert, Wolfgang BMC Bioinformatics Research Article BACKGROUND: Stimulus Response Experiments to unravel the regulatory properties of metabolic networks are becoming more and more popular. However, their ability to determine enzyme kinetic parameters has proven to be limited with the presently available data. In metabolic flux analysis, the use of (13)C labeled substrates together with isotopomer modeling solved the problem of underdetermined networks and increased the accuracy of flux estimations significantly. RESULTS: In this contribution, the idea of increasing the information content of the dynamic experiment by adding (13)C labeling is analyzed. For this purpose a small example network is studied by simulation and statistical methods. Different scenarios regarding available measurements are analyzed and compared to a non-labeled reference experiment. Sensitivity analysis revealed a specific influence of the kinetic parameters on the labeling measurements. Statistical methods based on parameter sensitivities and different measurement models are applied to assess the information gain of the labeled stimulus response experiment. CONCLUSION: It was found that the use of a (specifically) labeled substrate will significantly increase the parameter estimation accuracy. An overall information gain of about a factor of six is observed for the example network. The information gain is achieved from the specific influence of the kinetic parameters towards the labeling measurements. This also leads to a significant decrease in correlation of the kinetic parameters compared to an experiment without (13)C-labeled substrate. BioMed Central 2008-03-18 /pmc/articles/PMC2373788/ /pubmed/18366666 http://dx.doi.org/10.1186/1471-2105-9-152 Text en Copyright © 2008 Wahl et al; 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 Wahl, Sebastian Aljoscha Nöh, Katharina Wiechert, Wolfgang (13)C labeling experiments at metabolic nonstationary conditions: An exploratory study |
title | (13)C labeling experiments at metabolic nonstationary conditions: An exploratory study |
title_full | (13)C labeling experiments at metabolic nonstationary conditions: An exploratory study |
title_fullStr | (13)C labeling experiments at metabolic nonstationary conditions: An exploratory study |
title_full_unstemmed | (13)C labeling experiments at metabolic nonstationary conditions: An exploratory study |
title_short | (13)C labeling experiments at metabolic nonstationary conditions: An exploratory study |
title_sort | (13)c labeling experiments at metabolic nonstationary conditions: an exploratory study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2373788/ https://www.ncbi.nlm.nih.gov/pubmed/18366666 http://dx.doi.org/10.1186/1471-2105-9-152 |
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