Evidence map›Paper›PMID 31344404›Full record

ReviewMethods (San Diego, Calif.)2020

Strategies to maximize performance in STimulated Emission Depletion (STED) nanoscopy of biological specimens.

Wiebke Jahr, Philipp Velicky, Johann Georg Danzl

Abstract readReview
In one paragraph

Review in Methods (San Diego, Calif.), 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
–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

31 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. STED Super-Resolution Microscopy for Studying Actin Cytoskeleton Organization.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Identifying STEDable BFMolecules (Basel, Switzerland) · 2023
    Article
  20. Deep learning enables fast, gentle STED microscopy.bioRxiv : the preprint server for biology · 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

3 authors.

Wiebke JahrInstitute of Science and Technology Austria, Am Campus 1, 3400 Klosterneuburg, Austria.
Philipp VelickyInstitute of Science and Technology Austria, Am Campus 1, 3400 Klosterneuburg, Austria.
Johann Georg DanzlInstitute of Science and Technology Austria, Am Campus 1, 3400 Klosterneuburg, Austria. Electronic address: johann.danzl@ist.ac.at.

Funding

Austrian Science Fund FWF I 3600
6 · The paper itself

Abstract

Super-resolution fluorescence microscopy has become an important catalyst for discovery in the life sciences. In STimulated Emission Depletion (STED) microscopy, a pattern of light drives fluorophores from a signal-emitting on-state to a non-signalling off-state. Only emitters residing in a sub-diffraction volume around an intensity minimum are allowed to fluoresce, rendering them distinguishable from the nearby, but dark fluorophores. STED routinely achieves resolution in the few tens of nanometers range in biological samples and is suitable for live imaging. Here, we review the working principle of STED and provide general guidelines for successful STED imaging. The strive for ever higher resolution comes at the cost of increased light burden. We discuss techniques to reduce light exposure and mitigate its detrimental effects on the specimen. These include specialized illumination strategies as well as protecting fluorophores from photobleaching mediated by high-intensity STED light. This opens up the prospect of volumetric imaging in living cells and tissues with diffraction-unlimited resolution in all three spatial dimensions.

Indexed as

ColorEquipment ReuseFluorescenceFluorescent DyesImage Processing, Computer-AssistedLightingMicroscopy, FluorescenceOptical ImagingPhotobleachingScientific Experimental ErrorTime FactorsFluorescent DyesFluorescence microscopyLive imagingNanoscopyOptical imagingProtected STEDSTEDStimulated emission depletion microscopySuper-resolution microscopy

Identifiers

PMID31344404
PMCPMC7100895

What OpenQuestion holds

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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.