Evidence map›Paper›PMID 37751691›Full record

ArticleCell reports methods2023

Assessing crosstalk in simultaneous multicolor single-molecule localization microscopy.

Karoline Friedl, Adrien Mau, Fanny Boroni-Rueda, Valentina Caorsi, Nicolas Bourg, Sandrine Lévêque-Fort, Christophe Leterrier

Abstract read
In one paragraph

Article in Cell reports methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Electrochemical Dye Switching Assisted Spectral Demixing and 3D STORM Imaging.Angewandte Chemie (International ed. in English) · 2026
    Article
  4. Article
  5. Deciphering the Nanoscale Architecture of Presynaptic Actin Using a Micropatterned Presynapse-on-Glass Model.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Distinct SAP102 and PSD-95 Nano-organization Defines Multiple Types of Synaptic Scaffold Protein Domains at Single Synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  16. 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

7 authors.

Karoline FriedlAix Marseille Université, CNRS, INP UMR7051, NeuroCyto, 13005 Marseille, France; Abbelight, 191 Avenue Aristide Briand, 94230 Cachan, France.
Adrien MauAbbelight, 191 Avenue Aristide Briand, 94230 Cachan, France; Université Paris Saclay, CNRS, Institut des Sciences Moléculaires d'Orsay, 91405 Orsay, France.
Fanny Boroni-RuedaAix Marseille Université, CNRS, INP UMR7051, NeuroCyto, 13005 Marseille, France.
Valentina CaorsiAbbelight, 191 Avenue Aristide Briand, 94230 Cachan, France.
Nicolas BourgAbbelight, 191 Avenue Aristide Briand, 94230 Cachan, France.
Sandrine Lévêque-FortUniversité Paris Saclay, CNRS, Institut des Sciences Moléculaires d'Orsay, 91405 Orsay, France.
Christophe LeterrierAix Marseille Université, CNRS, INP UMR7051, NeuroCyto, 13005 Marseille, France. Electronic address: christophe.leterrier@univ-amu.fr.

Funding

EPA EP-D-16-021
6 · The paper itself

Abstract

Single-molecule localization microscopy (SMLM) can reach sub-50 nm resolution using techniques such as stochastic optical reconstruction microscopy (STORM) or DNA-point accumulation for imaging in nanoscale topography (PAINT). Here we implement two approaches for faster multicolor SMLM by splitting the emitted fluorescence toward two cameras: simultaneous two-color DNA-PAINT (S2C-DNA-PAINT) that images spectrally separated red and far-red imager strands on each camera, and spectral demixing dSTORM (SD-dSTORM) where spectrally close far-red fluorophores appear on both cameras before being identified by demixing. Using S2C-DNA-PAINT as a reference for low crosstalk, we evaluate SD-dSTORM crosstalk using three types of samples: DNA origami nanorulers of different sizes, single-target labeled cells, or cells labeled for multiple targets. We then assess if crosstalk can affect the detection of biologically relevant subdiffraction patterns. Extending these approaches to three-dimensional acquisition and SD-dSTORM to three-color imaging, we show that spectral demixing is an attractive option for robust and versatile multicolor SMLM investigations.

Indexed as

DNASingle Molecule ImagingMicroscopy, FluorescenceDNACP: ImagingcrosstalkDNA-PAINTdSTORMfluorescencemulticolormultitargetSMLMspectral demixingSTORMsuper resolution microscopy

Identifiers

PMID37751691
PMCPMC10545913

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.