Metabolic isotopomer labeling systems
Mathematical Biosciences, ISSN: 0025-5564, Vol: 169, Issue: 2, Page: 173-205
2001
- 52Citations
- 95Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations52
- Citation Indexes52
- 52
- CrossRef45
- Captures95
- Readers95
- Mentions1
- References1
- Wikipedia1
Article Description
In the last few years metabolic flux analysis (MFA) using carbon labeling experiments (CLE) has become a major diagnostic tool in metabolic engineering. The mathematical centerpiece of MFA is the solution of isotopomer labeling systems (ILS). An ILS is a high-dimensional nonlinear differential equation system that describes the distribution of isotopomers over a metabolic network during a carbon labeling experiment. This contribution presents a global analysis of the dynamic behavior of general ILSs. It is proven that an ILS is globally stable under very weak conditions that are always satisfied in practice. In particular it is shown that in some sense ILSs are a nonlinear extension to the classical theory of compartmental systems. The central stability condition for compartmental systems, i.e., the non-existence of traps in linear compartmental networks, is also the major stability condition for ILSs. As an important side result of the proof, it is shown that ILSs can be transformed to a cascade of linear systems with time-dependent inhomogeneous terms. This cascade structure has considerable consequences for the development of efficient numerical algorithms for the solution of ILSs and thus for MFA.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0025556400000596; http://dx.doi.org/10.1016/s0025-5564(00)00059-6; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0035101471&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/11166321; https://linkinghub.elsevier.com/retrieve/pii/S0025556400000596; http://linkinghub.elsevier.com/retrieve/pii/S0025556400000596; http://api.elsevier.com/content/article/PII:S0025556400000596?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0025556400000596?httpAccept=text/plain; http://dx.doi.org/10.1016/s0025-5564%2800%2900059-6; https://dx.doi.org/10.1016/s0025-5564%2800%2900059-6
Elsevier BV
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