Evidence map›Paper›PMID 38861534›Full record

ArticlePloS one2024

Alternative method to visualize receptor dynamics in cell membranes.

Ravelli Cosetta, Corsini Michela, Ventura Anna, Domenichini Mattia, Grillo Elisabetta, Mitola Stefania

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Ravelli CosettaDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Corsini MichelaDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.ORCID 0000-0002-8673-4376
Ventura AnnaDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Domenichini MattiaDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Grillo ElisabettaDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.ORCID 0000-0002-8403-0607
Mitola StefaniaDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.ORCID 0000-0002-5557-738X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a close relation between membrane receptor dynamics and their behavior. Several microscopy techniques have been developed to study protein dynamics in live cells such as the Fluorescence Recovery After Photobleaching (FRAP) or the Single Particle Tracking (SPT). These methodologies require expensive instruments, are time consuming, allow the analysis of small portion of the cell or an extremely small number of receptors at a time. Here we propose a time-saving approach that allows to visualize the entire receptor pool and its localization in time. This protocol requires an epifluorescence microscope equipped for structured illuminated sectioning and for live cell imaging. It can be applied to characterize membrane receptor and multi protein complex and their response to activators or inhibitors. Image acquisition and analysis can be performed in two days, while cells and substratum preparation require a few minutes a day for three days.

Indexed as

Cell MembraneFluorescence Recovery After PhotobleachingMicroscopy, FluorescenceAnimalsHumansReceptors, Cell SurfaceReceptors, Cell Surface

Identifiers

PMID38861534
PMCPMC11166301

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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.