Evidence map›Paper›PMID 26410690›Full record

ArticleBMC systems biology2015

Impact of kinetic isotope effects in isotopic studies of metabolic systems.

Pierre Millard, Jean-Charles Portais, Pedro Mendes

Open access · diamondAbstract read
In one paragraph

Article in BMC systems biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 34 citations in OpenAlex.

  1. IntegrativemSystems · 2024
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. DeltaMS: a tool to track isotopologues in GC- and LC-MS data.Metabolomics : Official journal of the Metabolomic Society · 2018
    Article
  7. Article
  8. Article
  9. KineticScientific reports · 2017
    Article
  10. Article
  11. Article
  12. Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Pierre MillardMCISB, Manchester Institute of Biotechnology, University of Manchester, Manchester, UK. pierre.millard@insa-toulouse.fr.
Jean-Charles PortaisUniversité de Toulouse; INSA, UPS, INP; LISBP, Toulouse, France. jean-charles.portais@insa-toulouse.fr.
Pedro MendesMCISB, Manchester Institute of Biotechnology, University of Manchester, Manchester, UK. pedro.mendes@manchester.ac.uk.
University of Manchester · GBLaboratoire d'Ingénierie des Systèmes Biologiques et des Procédés · FR

Funding

COPASI software for modeling and simulation of biochemical networksR01GM080219 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI HOOPS, STEFAN, MENDES, PEDRO · 2007 to 2019
$5.4M
Biotechnology and Biological Sciences Research Council BB/J019259/1Biotechnology and Biological Sciences Research Council BB/K019783/1NIGMS NIH HHS GM080219NIGMS NIH HHS R01 GM080219
6 · The paper itself

Abstract

backgroundIsotope labeling experiments (ILEs) are increasingly used to investigate the functioning of metabolic systems. Some enzymes are subject to kinetic isotope effects (KIEs) which modulate reaction rates depending on the isotopic composition of their substrate(s). KIEs may therefore affect both the propagation of isotopes through metabolic networks and their operation, and ultimately jeopardize the biological value of ILEs. However, the actual impact of KIEs on metabolism has never been investigated at the system level.

resultsFirst, we developed a framework which integrates KIEs into kinetic and isotopic models of metabolism, thereby accounting for their system-wide effects on metabolite concentrations, metabolic fluxes, and isotopic patterns. Then, we applied this framework to assess the impact of KIEs on the central carbon metabolism of Escherichia coli in the context of (13)C-ILEs, under different situations commonly encountered in laboratories. Results showed that the impact of KIEs strongly depends on the label input and on the variable considered but is significantly lower than expected intuitively from measurements on isolated enzymes. The global robustness of both the metabolic operation and isotopic patterns largely emerge from intrinsic properties of metabolic networks, such as the distribution of control across the network and bidirectional isotope exchange.

conclusionsThese results demonstrate the necessity of investigating the impact of KIEs at the level of the entire system, contradict previous hypotheses that KIEs would have a strong effect on isotopic distributions and on flux determination, and strengthen the biological value of (13)C-ILEs. The proposed modeling framework is generic and can be used to investigate the impact of all the isotopic tracers ((2)H, (13)C, (15)N, (18)O, etc.) on different isotopic datasets and metabolic systems. By allowing the integration of isotopic and metabolomics data collected under stationary and/or non-stationary conditions, it may also assist interpretations of ILEs and facilitate the development of more accurate kinetic models with improved explicative and predictive capabilities.

Indexed as

Carbon IsotopesEnzymesEscherichia coliSystems BiologyCarbon IsotopesEnzymes

Identifiers

PMID26410690
PMCPMC4583766
OpenAlexW2129845313

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.