Evidence map›Paper›PMID 20627152›Full record

ArticleMethods in enzymology2010

Molecules and methods for super-resolution imaging.

Michael A Thompson, Julie S Biteen, Samuel J Lord, Nicholas R Conley, W E Moerner

Abstract read
In one paragraph

Article in Methods in enzymology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Small Fluorogenic Amino Acids for Peptide-Guided Background-Free Imaging.Angewandte Chemie (International ed. in English) · 2023
    Article
  3. Small Fluorogenic Amino Acids for Peptide-Guided Background-Free Imaging.Angewandte Chemie (Weinheim an der Bergstrasse, Germany) · 2023
    Article
  4. Review
  5. Nanometer-Scale Molecular Mapping by Super-resolution Fluorescence Microscopy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. Quantum Dots for Improved Single-Molecule Localization Microscopy.The journal of physical chemistry. B · 2021
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Image analysis in fluorescence microscopy: bacterial dynamics as a case study.BioEssays : news and reviews in molecular, cellular and developmental biology · 2012
    Review
  18. Article
  19. Review of advanced imaging techniques.Journal of pathology informatics · 2012
    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

5 authors.

Michael A ThompsonDepartment of Chemistry, Stanford University, Stanford, California, USA.
Julie S Biteen
Samuel J Lord
Nicholas R Conley
W E Moerner

Funding

Subcellular architecture of regulatory protein complexes at the bacterial poleR01GM086196 · NIGMS · STANFORD UNIVERSITY · PI MOERNER, WILLIAM E, SHAPIRO, LUCILLE · 2008 to 2015
$4.7M
Single-Molecule Fluorophores for Cellular Imaging(RMI)P20HG003638 · NHGRI · STANFORD UNIVERSITY · PI MOERNER, WILLIAM E · 2004 to 2008
$3.0M
Three-Dimensional Superresolution Imaging in Living Cells Using Single-Molecule AR01GM085437 · NIGMS · STANFORD UNIVERSITY · PI MOERNER, WILLIAM E · 2008 to 2015
$2.1M
NHGRI NIH HHS 1P20-HG003638NHGRI NIH HHS P20 HG003638NIGMS NIH HHS R01 GM085437NIGMS NIH HHS R01GM085437NIGMS NIH HHS R01 GM086196
6 · The paper itself

Abstract

By looking at a fluorescently labeled structure one molecule at a time, it is possible to side-step the optical diffraction limit and obtain "super-resolution" images of small nanostructures. In the Moerner Lab, we seek to develop both molecules and methods to extend super-resolution fluorescence imaging. Methodologies and protocols for designing and characterizing fluorophores with switchable fluorescence required for super-resolution imaging are reported. These fluorophores include azido-DCDHF molecules, covalently linked Cy3-Cy5 dimers, and also the first example of a photoswitchable fluorescent protein, enhanced yellow fluorescent protein (EYFP). The imaging of protein superstructures in living Caulobacter crescentus bacteria is used as an example of the power of super-resolution imaging by single-molecule photoswitching to extract information beyond the diffraction limit. Finally, a new method is described for obtaining three-dimensional super-resolution information using a double-helix point-spread function.

Indexed as

Fluorescent DyesPhotonsAnimalsAzidesBacteriaHumansImaging, Three-DimensionalMicroscopy, FluorescenceMolecular StructurePhotochemistryAzidesFluorescent Dyes

Identifiers

PMID20627152
PMCPMC3216693

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.