Evidence map›Paper›PMID 30150727›Full record

ArticleNature chemistry2018

A fluorescent membrane tension probe.

Adai Colom, Emmanuel Derivery, Saeideh Soleimanpour, Caterina Tomba, Marta Dal Molin, Naomi Sakai, Marcos González-Gaitán, Stefan Matile, Aurélien Roux

Open access · greenAbstract read
In one paragraph

Article in Nature chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 258 papers.

0numbers the graph read from it
0cells of the map it votes in
258citing papers in PubMed
17.3field-weighted citation impact, top 1% 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

258 citing papers in PubMed, 557 citations in OpenAlex.

  1. Review
  2. Review
  3. Mechanical forces stimulate Golgi export.The Journal of cell biology · 2026
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  10. A Cholesterol Analogue for Cell-Surface Enzyme Display.Angewandte Chemie (International ed. in English) · 2026
    Article
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  14. Article
  15. Article
  16. Review
  17. Tension TRAAKer: a chemigenetic fluorescent membrane tension reporter.bioRxiv : the preprint server for biology · 2026
    Article
  18. Fluorescence-lifetime optical electrophysiology in contracting cardiomyocytes.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  19. Article
  20. Article

198 more citing papers are in PubMed but not listed here.

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 1 institution in 2 countries.

Adai ColomBiochemistry Department, University of Geneva, Geneva, Switzerland.
Emmanuel DeriveryBiochemistry Department, University of Geneva, Geneva, Switzerland.
Saeideh SoleimanpourSwiss National Centre for Competence in Research Programme Chemical Biology, Geneva, Switzerland.
Caterina TombaBiochemistry Department, University of Geneva, Geneva, Switzerland.
Marta Dal MolinSwiss National Centre for Competence in Research Programme Chemical Biology, Geneva, Switzerland.
Naomi SakaiSwiss National Centre for Competence in Research Programme Chemical Biology, Geneva, Switzerland.
Marcos González-GaitánBiochemistry Department, University of Geneva, Geneva, Switzerland.
Stefan MatileSwiss National Centre for Competence in Research Programme Chemical Biology, Geneva, Switzerland.
Aurélien RouxBiochemistry Department, University of Geneva, Geneva, Switzerland. Aurelien.Roux@unige.ch.ORCID http://orcid.org/0000-0002-6088-0711
University of Geneva · CH

Funding

European Research Council 311536Medical Research Council MC_UP_1201/13
6 · The paper itself

Abstract

Cells and organelles are delimited by lipid bilayers in which high deformability is essential to many cell processes, including motility, endocytosis and cell division. Membrane tension is therefore a major regulator of the cell processes that remodel membranes, albeit one that is very hard to measure in vivo. Here we show that a planarizable push-pull fluorescent probe called FliptR (fluorescent lipid tension reporter) can monitor changes in membrane tension by changing its fluorescence lifetime as a function of the twist between its fluorescent groups. The fluorescence lifetime depends linearly on membrane tension within cells, enabling an easy quantification of membrane tension by fluorescence lifetime imaging microscopy. We further show, using model membranes, that this linear dependency between lifetime of the probe and membrane tension relies on a membrane-tension-dependent lipid phase separation. We also provide calibration curves that enable accurate measurement of membrane tension using fluorescence lifetime imaging microscopy.

Indexed as

AnimalsCell MembraneDogsFluorescent DyesHeLa CellsHumansLipidsMadin Darby Canine Kidney CellsMicroscopy, FluorescenceOsmotic PressureFluorescent DyesLipids

Identifiers

PMID30150727
PMCPMC6197433
OpenAlexW2888670687

What OpenQuestion holds

Textmetadata
LicenceTDM
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.