Evidence map›Paper›PMID 32875078›Full record

ArticleACS central science2020

HaloFlippers: A General Tool for the Fluorescence Imaging of Precisely Localized Membrane Tension Changes in Living Cells.

Karolína Straková, Javier López-Andarias, Noemi Jiménez-Rojo, Joseph E Chambers, Stefan J Marciniak, Howard Riezman, Naomi Sakai, Stefan Matile

Open access · diamondAbstract read
In one paragraph

Article in ACS central science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Synthetic Lipid Biology.Chemical reviews · 2025
    Review
  6. Article
  7. Review
  8. Fluorescent Solvatochromic Probes for Long-Term Imaging of Lipid Order in Living Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Article
  10. Subphthalocyanine-flipper dyads for selective membrane staining.Physical chemistry chemical physics : PCCP · 2024
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. 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

8 authors at 2 institutions in 2 countries.

Karolína StrakováSchool of Chemistry and Biochemistry and National Centre of Competence in Research (NCCR) Chemical Biology, University of Geneva, Geneva 1211, Switzerland.
Javier López-AndariasSchool of Chemistry and Biochemistry and National Centre of Competence in Research (NCCR) Chemical Biology, University of Geneva, Geneva 1211, Switzerland.
Noemi Jiménez-RojoSchool of Chemistry and Biochemistry and National Centre of Competence in Research (NCCR) Chemical Biology, University of Geneva, Geneva 1211, Switzerland.
Joseph E ChambersCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom.
Stefan J MarciniakCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom.
Howard RiezmanSchool of Chemistry and Biochemistry and National Centre of Competence in Research (NCCR) Chemical Biology, University of Geneva, Geneva 1211, Switzerland.
Naomi SakaiSchool of Chemistry and Biochemistry and National Centre of Competence in Research (NCCR) Chemical Biology, University of Geneva, Geneva 1211, Switzerland.
Stefan MatileSchool of Chemistry and Biochemistry and National Centre of Competence in Research (NCCR) Chemical Biology, University of Geneva, Geneva 1211, Switzerland.
University of Geneva · CHUniversity of Cambridge · GB

Funding

Medical Research Council G1002610Medical Research Council MR/R009120/1
6 · The paper itself

Abstract

Tools to image membrane tension in response to mechanical stimuli are badly needed in mechanobiology. We have recently introduced mechanosensitive flipper probes to report quantitatively global membrane tension changes in fluorescence lifetime imaging microscopy (FLIM) images of living cells. However, to address specific questions on physical forces in biology, the probes need to be localized precisely in the membrane of interest (MOI). Herein we present a general strategy to image the tension of the MOI by tagging our newly introduced HaloFlippers to self-labeling HaloTags fused to proteins in this membrane. The critical challenge in the construction of operational HaloFlippers is the tether linking the flipper and the HaloTag: It must be neither too taut nor too loose, be hydrophilic but lipophilic enough to passively diffuse across membranes to reach the HaloTags, and allow partitioning of flippers into the MOI after the reaction. HaloFlippers with the best tether show localized and selective fluorescence after reacting with HaloTags that are close enough to the MOI but remain nonemissive if the MOI cannot be reached. Their fluorescence lifetime in FLIM images varies depending on the nature of the MOI and responds to myriocin-mediated sphingomyelin depletion as well as to osmotic stress. The response to changes in such precisely localized membrane tension follows the validated principles, thus confirming intact mechanosensitivity. Examples covered include HaloTags in the Golgi apparatus, peroxisomes, endolysosomes, and the ER, all thus becoming accessible to the selective fluorescence imaging of membrane tension.

Identifiers

PMID32875078
PMCPMC7453570
OpenAlexW3042296446

What OpenQuestion holds

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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.