Evidence map›Paper›PMID 39558589›Full record

ArticleBioinformatics (Oxford, England)2024

Sensitivities in protein allocation models reveal distribution of metabolic capacity and flux control.

Samira van den Bogaard, Pedro A Saa, Tobias B Alter

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Metabolic Fluxes Using Deep Learning Based on Enzyme Variations:International journal of molecular sciences · 2024
    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.

Samira van den BogaardInstitute of Applied Microbiology, Aachen Biology and Biotechnology, RWTH Aachen University, Aachen 52074, Germany.
Pedro A SaaDepartamento de Ingeniería Química y Bioprocesos, Escuela de Ingeniería, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile.
Tobias B AlterInstitute of Applied Microbiology, Aachen Biology and Biotechnology, RWTH Aachen University, Aachen 52074, Germany.ORCID 0000-0002-9593-4388

Funding

Ministry of Innovation, Science and Research of the German 313/323-400-00213
6 · The paper itself

Abstract

motivationExpanding on constraint-based metabolic models, protein allocation models (PAMs) enhance flux predictions by accounting for protein resource allocation in cellular metabolism. Yet, to this date, there are no dedicated methods for analyzing and understanding the growth-limiting factors in simulated phenotypes in PAMs.

resultsHere, we introduce a systematic framework for identifying the most sensitive enzyme concentrations (sEnz) in PAMs. The framework exploits the primal and dual formulations of these models to derive sensitivity coefficients based on relations between variables, constraints, and the objective function. This approach enhances our understanding of the growth-limiting factors of metabolic phenotypes under specific environmental or genetic conditions. Compared to other traditional methods for calculating sensitivities, sEnz requires substantially less computation time and facilitates more intuitive comparison and analysis of sensitivities. The sensitivities calculated by sEnz cover enzymes, reactions and protein sectors, enabling a holistic overview of the factors influencing metabolism. When applied to an Escherichia coli PAM, sEnz revealed major pathways and enzymes driving overflow metabolism. Overall, sEnz offers a computational efficient framework for understanding PAM predictions and unraveling the factors governing a particular metabolic phenotype. AVAILABILITY AND IMPLEMENTATION: sEnz is implemented in the modular toolbox for the generation and analysis of PAMs in Python (PAModelpy; v.0.0.3.3), available on Pypi (https://pypi.org/project/PAModelpy/). The source code together with all other python scripts and notebooks are available on GitHub (https://github.com/iAMB-RWTH-Aachen/PAModelpy).

Indexed as

Escherichia coliModels, BiologicalMetabolic Flux AnalysisMetabolic Networks and PathwaysSoftware

Identifiers

PMID39558589
PMCPMC11631525

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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.