Evidence map›Paper›PMID 20966075›Full record

ArticleThe Journal of biological chemistry2010

Imaging of mobile long-lived nanoplatforms in the live cell plasma membrane.

Mario Brameshuber, Julian Weghuber, Verena Ruprecht, Imre Gombos, Ibolya Horváth, László Vigh, Paul Eckerstorfer, Endre Kiss, Hannes Stockinger, Gerhard J Schütz

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 115 citations in OpenAlex.

  1. Trial
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  5. Analytical Techniques for Single-Cell Biochemical Assays of Lipids.Annual review of biomedical engineering · 2023
    Review
  6. Article
  7. Article
  8. The plasma membrane as an adaptable fluid mosaic.Biochimica et biophysica acta. Biomembranes · 2023
    Review
  9. Article
  10. Calcium levels in the Golgi complex regulate clustering and apical sorting of GPI-APs in polarized epithelial cells.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Article
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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

10 authors at 3 institutions in 2 countries.

Mario BrameshuberBiophysics Institute, Johannes Kepler University Linz, Altenbergerstrasse 69, A-4040 Linz, Austria.
Julian Weghuber
Verena Ruprecht
Imre Gombos
Ibolya Horváth
László Vigh
Paul Eckerstorfer
Endre Kiss
Hannes Stockinger
Gerhard J Schütz
Johannes Kepler University of Linz · ATHUN-REN Szegedi Biológiai Kutatóközpont · HUMedical University of Vienna · AT

Funding

Austrian Science Fund FWF I 300Austrian Science Fund FWF Y 250
6 · The paper itself

Abstract

The plasma membrane has been hypothesized to contain nanoscopic lipid platforms, which are discussed in the context of "lipid rafts" or "membrane rafts." Based on biochemical and cell biological studies, rafts are believed to play a crucial role in many signaling processes. However, there is currently not much information on their size, shape, stability, surface density, composition, and heterogeneity. We present here a method that allows for the first time the direct imaging of nanoscopic long-lived platforms with raft-like properties diffusing in the live cell plasma membrane. Our method senses these platforms by their property to assemble a characteristic set of fluorescent marker proteins or lipids on a time scale of seconds. A special photobleaching protocol was used to reduce the surface density of labeled mobile platforms down to the level of well isolated diffraction-limited spots without altering the single spot brightness. The statistical distribution of probe molecules per platform was determined by single molecule brightness analysis. For demonstration, we used the consensus raft marker glycosylphosphatidylinositol-anchored monomeric GFP and the fluorescent lipid analog BODIPY-G(M1), which preferentially partitions into liquid-ordered phases. For both markers, we found cholesterol-dependent homo-association in the plasma membrane of living CHO and Jurkat T cells in the resting state, thereby demonstrating the existence of small, mobile, long-lived platforms containing these probes. We further applied the technology to address structural changes in the plasma membrane during fever-type heat shock: at elevated temperatures, the glycosylphosphatidylinositol-anchored monomeric GFP homo-association disappeared, accompanied by an increase in the expression of the small heat shock protein Hsp27.

Indexed as

AnimalsCell MembraneCholesterolCricetinaeCricetulusDiffusionGlycosylphosphatidylinositolsGreen Fluorescent ProteinsHumansJurkat CellsMembrane MicrodomainsMicroscopyNanostructuresNanotechnologySurface PropertiesCholesterolGlycosylphosphatidylinositolsGreen Fluorescent Proteins

Identifiers

PMID20966075
PMCPMC3009904
OpenAlexW1996968937

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.