Evidence map›Paper›PMID 26091700›Full record

ArticleMolecular & cellular proteomics : MCP2015

Cytoskeletal Components Define Protein Location to Membrane Microdomains.

Witold G Szymanski, Henrik Zauber, Alexander Erban, Michal Gorka, Xu Na Wu, Waltraud X Schulze

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Myosin XI-mediated BIK1 recruitment to nanodomains facilitates FLS2-BIK1 complex formation during innate immunity inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Membrane Dynamics Regulated by Cytoskeleton in Plant Immunity.International journal of molecular sciences · 2023
    Review
  4. Article
  5. The Cytoskeleton in Plant Immunity: Dynamics, Regulation, and Function.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Salt Stress Signals on Demand: Cellular Events in the Right Context.International journal of molecular sciences · 2020
    Review
  11. TheThe Plant cell · 2020
    Article
  12. Review
  13. Chloroplast Calcium Signaling in the Spotlight.Frontiers in plant science · 2020
    Review
  14. Organization and dynamics of functional plant membrane microdomains.Cellular and molecular life sciences : CMLS · 2020
    Review
  15. Article
  16. Article
  17. The cell wall regulates dynamics and size of plasma-membrane nanodomains inProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  18. Article
  19. Symbiotic root infections inProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  20. Feedback Microtubule Control and Microtubule-Actin Cross-talk inMolecular & cellular proteomics : MCP · 2017
    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

6 authors at 2 institutions in 1 country.

Witold G SzymanskiFrom the ‡Max Planck Institute of Molecular Plant Physiology, 14476 Potsdam, Germany;
Henrik Zauber§Max-Delbrück Center of Molecular Medicine, Robert-Rössle-Straβe 10, 13092 Berlin, Germany;
Alexander ErbanFrom the ‡Max Planck Institute of Molecular Plant Physiology, 14476 Potsdam, Germany;
Michal GorkaFrom the ‡Max Planck Institute of Molecular Plant Physiology, 14476 Potsdam, Germany;
Xu Na WuFrom the ‡Max Planck Institute of Molecular Plant Physiology, 14476 Potsdam, Germany;
Waltraud X Schulze¶University of Hohenheim, Department of Plant Systems Biology, 70593 Stuttgart, Germany wschulze@uni-hohenheim.de.
Max Planck Society · DEMax Delbrück Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The plasma membrane is an important compartment that undergoes dynamic changes in composition upon external or internal stimuli. The dynamic subcompartmentation of proteins in ordered low-density (DRM) and disordered high-density (DSM) membrane phases is hypothesized to require interactions with cytoskeletal components. Here, we systematically analyzed the effects of actin or tubulin disruption on the distribution of proteins between membrane density phases. We used a proteomic screen to identify candidate proteins with altered submembrane location, followed by biochemical or cell biological characterization in Arabidopsis thaliana. We found that several proteins, such as plasma membrane ATPases, receptor kinases, or remorins resulted in a differential distribution between membrane density phases upon cytoskeletal disruption. Moreover, in most cases, contrasting effects were observed: Disruption of actin filaments largely led to a redistribution of proteins from DRM to DSM membrane fractions while disruption of tubulins resulted in general depletion of proteins from the membranes. We conclude that actin filaments are necessary for dynamic movement of proteins between different membrane phases and that microtubules are not necessarily important for formation of microdomains as such, but rather they may control the protein amount present in the membrane phases.

Indexed as

ActinsArabidopsisArabidopsis ProteinsCell Culture TechniquesCell MembraneProteomicsTubulinActinsArabidopsis ProteinsTubulin

Identifiers

PMID26091700
PMCPMC4563731
OpenAlexW1937296368

What OpenQuestion holds

Textmetadata
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.