Evidence map›Paper›PMID 30874551›Full record

ArticleNature communications2019

Photoregulated fluxional fluorophores for live-cell super-resolution microscopy with no apparent photobleaching.

Elias A Halabi, Dorothea Pinotsi, Pablo Rivera-Fuentes

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In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

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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

3 authors.

Elias A HalabiLaboratory of Organic Chemistry, ETH Zurich, Zurich, 8093, Switzerland.
Dorothea PinotsiScientific Center for Optical and Electron Microscopy, ETH Zurich, Zurich, 8093, Switzerland.
Pablo Rivera-FuentesLaboratory of Organic Chemistry, ETH Zurich, Zurich, 8093, Switzerland. pablo.rivera-fuentes@org.chem.ethz.ch.ORCID http://orcid.org/0000-0001-8558-2828

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photoswitchable molecules have multiple applications in the physical and life sciences because their properties can be modulated with light. Fluxional molecules, which undergo rapid degenerate rearrangements in the electronic ground state, also exhibit switching behavior. The stochastic nature of fluxional switching, however, has hampered its application in the development of functional molecules and materials. Here we combine photoswitching and fluxionality to develop a fluorophore that enables very long (>30 min) time-lapse single-molecule localization microscopy in living cells with minimal phototoxicity and no apparent photobleaching. These long time-lapse experiments allow us to track intracellular organelles with unprecedented spatiotemporal resolution, revealing new information of the three-dimensional compartmentalization of synaptic vesicle trafficking in live human neurons.

Indexed as

Fluorescent DyesHeLa CellsHumansIntravital MicroscopyIsomerismLightMicroscopy, FluorescenceMolecular ProbesNeuronsPhotobleachingSingle Molecule ImagingSpectrometry, FluorescenceSynaptic VesiclesTime-Lapse ImagingFluorescent DyesMolecular Probes

Identifiers

PMID30874551
PMCPMC6420572

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.