Evidence map›Paper›PMID 22068155›Full record

ArticleJournal of structural biology2012

Metallothionein as a clonable high-density marker for cryo-electron microscopy.

Cédric Bouchet-Marquis, Maria Pagratis, Robert Kirmse, Andreas Hoenger

Abstract read
In one paragraph

Article in Journal of structural biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Molecular tags for electron cryo-tomography.Emerging topics in life sciences · 2025
    Review
  2. Article
  3. Charting the molecular landscape of the cell.Structure (London, England : 1993) · 2023
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Lessons from yeast: the spindle pole body and the centrosome.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Review
  12. Article
  13. Review
  14. Article
  15. Golgi apparatus analyzed by cryo-electron microscopy.Histochemistry and cell biology · 2013
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

4 authors.

Cédric Bouchet-MarquisDept. of Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, CO 80309-0347, USA.
Maria Pagratis
Robert Kirmse
Andreas Hoenger

Funding

WORKSHOPS AND TRAINING FOR IMAGE ANALYSIS USING IMODP41RR000592 · NCRR · UNIVERSITY OF COLORADO AT BOULDER · PI BASS, PETER W. · 1985 to 2011
$11.9M
A Clonable High-Density for 3-D Electron Microscopy of Cellular StructuresR01GM080993 · NIGMS · UNIVERSITY OF COLORADO · PI HOENGER, ANDREAS · 2007 to 2010
$1.0M
NCRR NIH HHS 2P41-RR000592NCRR NIH HHS P41 RR000592NIGMS NIH HHS 5R01-GM80993NIGMS NIH HHS R01 GM080993
6 · The paper itself

Abstract

Cryo-electron microscopy is expanding its scope from macromolecules towards much larger and more complex cellular specimens such as organelles, cells and entire tissues. While isolated macromolecular specimens are typically composed of only very few different components that may be recognized by their shape, size or state of polymerization, cellular specimens combine large numbers of proteinaceous structures as well as nucleic acids and lipid arrays. Consequently, an unambiguous identification of these structures within the context of a whole cell may create a very difficult challenge. On plastic-embedded specimens, or Tokuyasu sections (Tokuyasu, 1980), epitopes that are exposed at the surface can be tagged by antibodies. However, vitrified sections have to be kept at strict cryo-conditions (below -140 °C) and therefore do not allow any post-sectioning treatment of the specimens other than data acquisition in the microscope. Hence, the labels have to be placed into the specimen before freezing. Here we report on the application of a small metal-clustering protein, metallothionein (MTH), as a clonable label capable of clustering metal atoms into a high-density particle with high spatial resolution. We tested MTH as a label for kinesin-decorated microtubules (MTs) as well as the building blocks of desmin intermediate filaments (IFs).

Indexed as

Cloning, MolecularCryoelectron MicroscopyDesminGene Expression RegulationImage Processing, Computer-AssistedIntermediate FilamentsMetallothioneinMicrotubulesModels, MolecularOrganellesProtein Structure, TertiarySpecimen HandlingDesminMetallothionein

Identifiers

PMID22068155
PMCPMC3261350

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.