Evidence map›Paper›PMID 25422417›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Whole-cell, multicolor superresolution imaging using volumetric multifocus microscopy.

Bassam Hajj, Jan Wisniewski, Mohamed El Beheiry, Jiji Chen, Andrey Revyakin, Carl Wu, Maxime Dahan

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
11.6field-weighted citation impact, top 2% 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

49 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Highly sensitive volumetric single-molecule imaging.Nanophotonics (Berlin, Germany) · 2024
    Article
  12. Article
  13. Article
  14. Recent Advances in Single-Molecule Tracking and Imaging Techniques.Annual review of analytical chemistry (Palo Alto, Calif.) · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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 at 2 institutions in 2 countries.

Bassam HajjLaboratoire Physico-Chimie Curie, Institut Curie, CNRS UMR168, Université Pierre et Marie Curie-Paris 6, 75005 Paris, France; and Transcription Imaging Consortium, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Jan WisniewskiTranscription Imaging Consortium, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Mohamed El BeheiryLaboratoire Physico-Chimie Curie, Institut Curie, CNRS UMR168, Université Pierre et Marie Curie-Paris 6, 75005 Paris, France; and Transcription Imaging Consortium, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Jiji ChenTranscription Imaging Consortium, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Andrey RevyakinTranscription Imaging Consortium, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Carl WuTranscription Imaging Consortium, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Maxime DahanLaboratoire Physico-Chimie Curie, Institut Curie, CNRS UMR168, Université Pierre et Marie Curie-Paris 6, 75005 Paris, France; and Transcription Imaging Consortium, Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147 maxime.dahan@curie.fr.
Howard Hughes Medical Institute · USCentre National de la Recherche Scientifique · FR

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Single molecule-based superresolution imaging has become an essential tool in modern cell biology. Because of the limited depth of field of optical imaging systems, one of the major challenges in superresolution imaging resides in capturing the 3D nanoscale morphology of the whole cell. Despite many previous attempts to extend the application of photo-activated localization microscopy (PALM) and stochastic optical reconstruction microscopy (STORM) techniques into three dimensions, effective localization depths do not typically exceed 1.2 µm. Thus, 3D imaging of whole cells (or even large organelles) still demands sequential acquisition at different axial positions and, therefore, suffers from the combined effects of out-of-focus molecule activation (increased background) and bleaching (loss of detections). Here, we present the use of multifocus microscopy for volumetric multicolor superresolution imaging. By simultaneously imaging nine different focal planes, the multifocus microscope instantaneously captures the distribution of single molecules (either fluorescent proteins or synthetic dyes) throughout an ∼ 4-µm-deep volume, with lateral and axial localization precisions of ∼ 20 and 50 nm, respectively. The capabilities of multifocus microscopy to rapidly image the 3D organization of intracellular structures are illustrated by superresolution imaging of the mammalian mitochondrial network and yeast microtubules during cell division.

Indexed as

CalibrationFluorescent DyesGreen Fluorescent ProteinsHeLa CellsHumansImage Processing, Computer-AssistedImaging, Three-DimensionalMicroscopy, FluorescenceMitochondriaModels, MolecularReproducibility of ResultsSaccharomyces cerevisiaeFluorescent DyesGreen Fluorescent Proteins3D localizationmicroscopymultiplane imagingsingle-molecule fluorescencesuperresolution

Identifiers

PMID25422417
PMCPMC4267334
OpenAlexW1992893959

What OpenQuestion holds

Textmetadata
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.