Evidence map›Paper›PMID 36632034›Full record

ArticleBiophysical journal2023

Quantifying membrane binding and diffusion with fluorescence correlation spectroscopy diffusion laws.

Anita Mouttou, Erwan Bremaud, Julien Noero, Rayane Dibsy, Coline Arone, Johnson Mak, Delphine Muriaux, Hugues Berry, Cyril Favard

Open access · greenAbstract read
In one paragraph

Article in Biophysical journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
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  4. MNature communications · 2024
    Article
  5. Article
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  7. Membranes in focus.Biophysical journal · 2023
    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

9 authors at 3 institutions in 2 countries.

Anita MouttouMembrane Domains and Viral Assembly, Montpellier Infectious Disease Research Institute, UMR CNRS 9004, Montpellier, France.
Erwan BremaudMembrane Domains and Viral Assembly, Montpellier Infectious Disease Research Institute, UMR CNRS 9004, Montpellier, France.
Julien NoeroMembrane Domains and Viral Assembly, Montpellier Infectious Disease Research Institute, UMR CNRS 9004, Montpellier, France.
Rayane DibsyMembrane Domains and Viral Assembly, Montpellier Infectious Disease Research Institute, UMR CNRS 9004, Montpellier, France.
Coline AroneMembrane Domains and Viral Assembly, Montpellier Infectious Disease Research Institute, UMR CNRS 9004, Montpellier, France.
Johnson MakInstitute for Glycomics, Griffith University Gold Coast, Southport, QLD, Australia.
Delphine MuriauxMembrane Domains and Viral Assembly, Montpellier Infectious Disease Research Institute, UMR CNRS 9004, Montpellier, France.
Hugues BerryINRIA Rhone Alpes, Laboratoire d'InfoRmatique en Image et Systèmes d'information, UMR 5205 CNRS INSA Lyon, Université Claude Bernard Lyon 1, Université Lumière Lyon 2, École Centrale de Lyon, Campus de la Doua, Villeurbanne, France. Electronic address: hugues.berry@inria.fr.
Cyril FavardMembrane Domains and Viral Assembly, Montpellier Infectious Disease Research Institute, UMR CNRS 9004, Montpellier, France. Electronic address: cyril.favard@irim.cnrs.fr.
Centre National de la Recherche Scientifique · FRGriffith University · AUUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many transient processes in cells arise from the binding of cytosolic proteins to membranes. Quantifying this membrane binding and its associated diffusion in the living cell is therefore of primary importance. Dynamic photonic microscopies, e.g., single/multiple particle tracking, fluorescence recovery after photobleaching, and fluorescence correlation spectroscopy (FCS), enable non-invasive measurement of molecular mobility in living cells and their plasma membranes. However, FCS with a single beam waist is of limited applicability with complex, non-Brownian, motions. Recently, the development of FCS diffusion laws methods has given access to the characterization of these complex motions, although none of them is applicable to the membrane binding case at the moment. In this study, we combined computer simulations and FCS experiments to propose an FCS diffusion law for membrane binding. First, we generated computer simulations of spot-variation FCS (svFCS) measurements for a membrane binding process combined to 2D and 3D diffusion at the membrane and in the bulk/cytosol, respectively. Then, using these simulations as a learning set, we derived an empirical diffusion law with three free parameters: the apparent binding constant K

Indexed as

Lipid BilayersCell MembraneDiffusionMembranesSpectrometry, FluorescenceLipid Bilayers

Identifiers

PMID36632034
PMCPMC10257123
OpenAlexW4315490365

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.