Evidence map›Paper›PMID 32365103›Full record

ArticlePLoS computational biology2020

Robustness and parameter geography in post-translational modification systems.

Kee-Myoung Nam, Benjamin M Gyori, Silviana V Amethyst, Daniel J Bates, Jeremy Gunawardena

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Network regulation meets substrate modification chemistry.Journal of the Royal Society, Interface · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Mapping parameter spaces of biological switches.PLoS computational biology · 2021
    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

5 authors at 3 institutions in 1 country.

Kee-Myoung NamDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0002-3594-6141
Benjamin M GyoriLaboratory of Systems Pharmacology, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0001-9439-5346
Silviana V AmethystDepartment of Mathematics, University of Wisconsin-Eau Claire, Eau Claire, Wisconsin, United States of America.ORCID 0000-0001-7535-4602
Daniel J BatesDepartment of Mathematics, United States Naval Academy, Annapolis, Maryland, United States of America.ORCID 0000-0003-2985-0554
Jeremy GunawardenaDepartment of Systems Biology, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0002-7280-1152
Harvard University · USUnited States Naval Academy · USUniversity of Wisconsin–Eau Claire · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biological systems are acknowledged to be robust to perturbations but a rigorous understanding of this has been elusive. In a mathematical model, perturbations often exert their effect through parameters, so sizes and shapes of parametric regions offer an integrated global estimate of robustness. Here, we explore this "parameter geography" for bistability in post-translational modification (PTM) systems. We use the previously developed "linear framework" for timescale separation to describe the steady-states of a two-site PTM system as the solutions of two polynomial equations in two variables, with eight non-dimensional parameters. Importantly, this approach allows us to accommodate enzyme mechanisms of arbitrary complexity beyond the conventional Michaelis-Menten scheme, which unrealistically forbids product rebinding. We further use the numerical algebraic geometry tools Bertini, Paramotopy, and alphaCertified to statistically assess the solutions to these equations at ∼109 parameter points in total. Subject to sampling limitations, we find no bistability when substrate amount is below a threshold relative to enzyme amounts. As substrate increases, the bistable region acquires 8-dimensional volume which increases in an apparently monotonic and sigmoidal manner towards saturation. The region remains connected but not convex, albeit with a high visibility ratio. Surprisingly, the saturating bistable region occupies a much smaller proportion of the sampling domain under mechanistic assumptions more realistic than the Michaelis-Menten scheme. We find that bistability is compromised by product rebinding and that unrealistic assumptions on enzyme mechanisms have obscured its parametric rarity. The apparent monotonic increase in volume of the bistable region remains perplexing because the region itself does not grow monotonically: parameter points can move back and forth between monostability and bistability. We suggest mathematical conjectures and questions arising from these findings. Advances in theory and software now permit insights into parameter geography to be uncovered by high-dimensional, data-centric analysis.

Indexed as

AlgorithmsComputational BiologyGene ExpressionGene Regulatory NetworksModels, BiologicalModels, TheoreticalProtein Processing, Post-Translational

Identifiers

PMID32365103
PMCPMC7224580
OpenAlexW3023635562

What OpenQuestion holds

Textmetadata
LicenceCC0
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.