Evidence map›Paper›PMID 22253752›Full record

ArticlePloS one2012

Spatial modeling of vesicle transport and the cytoskeleton: the challenge of hitting the right road.

Michael Klann, Heinz Koeppl, Matthias Reuss

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. A multiscale model of the regulation of aquaporin 2 recycling.NPJ systems biology and applications · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Point process models for localization and interdependence of punctate cellular structures.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2016
    Article
  11. Article
  12. Article
  13. Involvement of small G proteins and vesicle traffic in the glutoxim and molixan effects on the intracellular Ca(2+) concentration in macrophages.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections · 2014
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Hybrid spatial Gillespie and particle tracking simulation.Bioinformatics (Oxford, England) · 2012
    Article
  19. From microscopy data to in silico environments for in vivo-oriented simulations.EURASIP journal on bioinformatics & systems biology · 2012
    Article
  20. Spatial simulations in systems biology: from molecules to cells.International journal of molecular sciences · 2012
    Review
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 3 institutions in 2 countries.

Michael KlannAutomatic Control Laboratory, Swiss Federal Institute of Technology Zurich, Zurich, Switzerland. mklann@control.ee.ethz.ch
Heinz Koeppl
Matthias Reuss
École Polytechnique Fédérale de Lausanne · CHETH Zurich · CHUniversity of Stuttgart · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The membrane trafficking machinery provides a transport and sorting system for many cellular proteins. We propose a mechanistic agent-based computer simulation to integrate and test the hypothesis of vesicle transport embedded into a detailed model cell. The method tracks both the number and location of the vesicles. Thus both the stochastic properties due to the low numbers and the spatial aspects are preserved. The underlying molecular interactions that control the vesicle actions are included in a multi-scale manner based on the model of Heinrich and Rapoport (2005). By adding motor proteins we can improve the recycling process of SNAREs and model cell polarization. Our model also predicts that coat molecules should have a high turnover at the compartment membranes, while the turnover of motor proteins has to be slow. The modular structure of the underlying model keeps it tractable despite the overall complexity of the vesicle system. We apply our model to receptor-mediated endocytosis and show how a polarized cytoskeleton structure leads to polarized distributions in the plasma membrane both of SNAREs and the Ste2p receptor in yeast. In addition, we can couple signal transduction and membrane trafficking steps in one simulation, which enables analyzing the effect of receptor-mediated endocytosis on signaling.

Indexed as

Models, BiologicalCell MembraneCell PolarityComputer SimulationCytoskeletonEndocytosisExocytosisKineticsProtein TransportReceptors, Cell SurfaceSignal TransductionReceptors, Cell Surface

Identifiers

PMID22253752
PMCPMC3257240
OpenAlexW2051245469

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.