Evidence map›Paper›PMID 31980680›Full record

ArticleScientific reports2020

Simultaneous co-localized super-resolution fluorescence microscopy and atomic force microscopy: combined SIM and AFM platform for the life sciences.

Ana I Gómez-Varela, Dimitar R Stamov, Adelaide Miranda, Rosana Alves, Cláudia Barata-Antunes, Daphné Dambournet, David G Drubin, Sandra Paiva, Pieter A A De Beule

Abstract read
In one paragraph

Article in Scientific reports, 2020. 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. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Visualizing Intramolecular Dynamics of Membrane Proteins.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Correlative AFM and Scanning Microlens Microscopy for Time-Efficient Multiscale Imaging.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  11. Quantifying molecular- to cellular-level forces in living cells.Journal of physics D: Applied physics · 2021
    Article
  12. Article
  13. Article
  14. AFM-Based Correlative Microscopy Illuminates Human Pathogens.Frontiers in cellular and infection microbiology · 2021
    Review
  15. Article
  16. Review
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

9 authors.

Ana I Gómez-VarelaInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga s/n, Braga, Portugal. anaisabel.gomez@usc.es.
Dimitar R StamovJPK BioAFM Business, Nano Surfaces Division, Bruker Nano GmbH, Am Studio 2D, 12489, Berlin, Germany.
Adelaide MirandaInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga s/n, Braga, Portugal.
Rosana AlvesCentre of Molecular and Environmental Biology, Department of Biology, University of Minho, Braga, Portugal.
Cláudia Barata-AntunesCentre of Molecular and Environmental Biology, Department of Biology, University of Minho, Braga, Portugal.
Daphné DambournetDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
David G DrubinDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Sandra PaivaCentre of Molecular and Environmental Biology, Department of Biology, University of Minho, Braga, Portugal.
Pieter A A De BeuleInternational Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga s/n, Braga, Portugal. pieter.de-beule@inl.int.

Funding

Nikon confocal system for improved spatio-dynamic analysis of endocytic trafficking eventsR35GM118149 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI DAVID G DRUBIN · 2016 to 2026
$12.0M
NIGMS NIH HHS R35 GM118149
6 · The paper itself

Abstract

Correlating data from different microscopy techniques holds the potential to discover new facets of signaling events in cellular biology. Here we report for the first time a hardware set-up capable of achieving simultaneous co-localized imaging of spatially correlated far-field super-resolution fluorescence microscopy and atomic force microscopy, a feat only obtained until now by fluorescence microscopy set-ups with spatial resolution restricted by the Abbe diffraction limit. We detail system integration and demonstrate system performance using sub-resolution fluorescent beads and applied to a test sample consisting of human bone osteosarcoma epithelial cells, with plasma membrane transporter 1 (MCT1) tagged with an enhanced green fluorescent protein (EGFP) at the N-terminal.

Identifiers

PMID31980680
PMCPMC6981207

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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.