Evidence map›Paper›PMID 21152415›Full record

ArticleCellular and molecular bioengineering2008

Model for Protein Concentration Gradients in the Cytoplasm.

Karen Lipkow, David J Odde

Abstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Internal feedback circuits among MEX-5, MEX-6, and PLK-1 maintain faithful patterning in theProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Anterior-posterior pattern formation in ciliates.The Journal of eukaryotic microbiology · 2022
    Review
  12. Modeling protein dynamics inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Persistent growth of microtubules at low density.Molecular biology of the cell · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Single-molecule study reveals the frenetic lives of proteins in gradients.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  19. Rapid diffusion-state switching underlies stable cytoplasmic gradients in theProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  20. 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

2 authors.

Karen LipkowPhysiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.
David J Odde

Funding

Modeling Microtubule Dynamics in MitosisR01GM071522 · NIGMS · UNIVERSITY OF MINNESOTA · PI ODDE, DAVID J. · 2006 to 2013
$2.7M
MOLECULAR EVENTS IN A DISCRETE CYTOPLASMIC SPACER01GM064713 · NIGMS · UNIVERSITY OF CAMBRIDGE · PI BRAY, DENNIS · 2002 to 2007
$1.1M
NIGMS NIH HHS R01 GM064713NIGMS NIH HHS R01 GM071522
6 · The paper itself

Abstract

Intracellular protein concentration gradients are generally thought to be unsustainable at steady-state due to diffusion. Here we show how protein concentration gradients can theoretically be sustained indefinitely through a relatively simple mechanism that couples diffusion to a spatially segregated kinase-phosphatase system. Although it is appreciated that such systems can theoretically give rise to phosphostate gradients, it has been assumed that they do not give rise to gradients in the total protein concentration. Here we show that this assumption does not hold if the two forms of protein have different diffusion coefficients. If, for example, the phosphorylated state binds selectively to a second larger protein or protein complex then a steady state gradient in total protein concentration will be created. We illustrate the principle with an analytical solution to the diffusion-reaction problem and by stochastic individual-based simulations using the Smoldyn program. We argue that protein gradients created in this way need to be considered in experiments using fluorescent probes and could in principle encode spatial information in the cytoplasm.

Identifiers

PMID21152415
PMCPMC2996619

What OpenQuestion holds

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Registered trials

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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.