Evidence map›Paper›PMID 18769681›Full record

ArticlePloS one2008

Global self-organization of the cellular metabolic structure.

Ildefonso M De La Fuente, Luis Martínez, Alberto L Pérez-Samartín, Leire Ormaetxea, Cristian Amezaga, Antonio Vera-López

Abstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

18 citing papers in PubMed.

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  8. Elements of the cellular metabolic structure.Frontiers in molecular biosciences · 2015
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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

6 authors.

Ildefonso M De La FuenteDepartamento de Matemáticas, Facultad de Ciencia y Tecnología, Universidad del País Vasco, Vizcaya, Spain.
Luis Martínez
Alberto L Pérez-Samartín
Leire Ormaetxea
Cristian Amezaga
Antonio Vera-López

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOver many years, it has been assumed that enzymes work either in an isolated way, or organized in small catalytic groups. Several studies performed using "metabolic networks models" are helping to understand the degree of functional complexity that characterizes enzymatic dynamic systems. In a previous work, we used "dissipative metabolic networks" (DMNs) to show that enzymes can present a self-organized global functional structure, in which several sets of enzymes are always in an active state, whereas the rest of molecular catalytic sets exhibit dynamics of on-off changing states. We suggested that this kind of global metabolic dynamics might be a genuine and universal functional configuration of the cellular metabolic structure, common to all living cells. Later, a different group has shown experimentally that this kind of functional structure does, indeed, exist in several microorganisms. METHODOLOGY/PRINCIPAL

findingsHere we have analyzed around 2.500.000 different DMNs in order to investigate the underlying mechanism of this dynamic global configuration. The numerical analyses that we have performed show that this global configuration is an emergent property inherent to the cellular metabolic dynamics. Concretely, we have found that the existence of a high number of enzymatic subsystems belonging to the DMNs is the fundamental element for the spontaneous emergence of a functional reactive structure characterized by a metabolic core formed by several sets of enzymes always in an active state. CONCLUSIONS/SIGNIFICANCE: This self-organized dynamic structure seems to be an intrinsic characteristic of metabolism, common to all living cellular organisms. To better understand cellular functionality, it will be crucial to structurally characterize these enzymatic self-organized global structures.

Indexed as

Cell Physiological PhenomenaCell CycleCellsEnzymesHomeostasisKineticsModels, BiologicalEnzymes

Identifiers

PMID18769681
PMCPMC2519785

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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.