Evidence map›Paper›PMID 31709058›Full record

ArticleIUCrJ2019

A cryo-EM grid preparation device for time-resolved structural studies.

Dimitrios Kontziampasis, David P Klebl, Matthew G Iadanza, Charlotte A Scarff, Florian Kopf, Frank Sobott, Diana C F Monteiro, Martin Trebbin, Stephen P Muench, Howard D White

Abstract read
In one paragraph

Article in IUCrJ, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

  1. Article
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  6. Article
  7. A Bright and Dynamic Future in Structural Biology.Advances in experimental medicine and biology · 2026
    Review
  8. Microfluidic Devices for High-Throughput In Situ Serial Crystallography.Advances in biochemical engineering/biotechnology · 2026
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Identifying intermolecular interactions in single-molecule localization microscopy.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

10 authors.

Dimitrios KontziampasisSchool of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, UK.ORCID https://orcid.org/0000-0002-6787-8892
David P KleblSchool of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, UK.ORCID https://orcid.org/0000-0002-3581-8334
Matthew G IadanzaSchool of Molecular and Cellular Biology, University of Leeds, Leeds LS2 9JT, UK.ORCID https://orcid.org/0000-0001-6152-1844
Charlotte A ScarffSchool of Molecular and Cellular Biology, University of Leeds, Leeds LS2 9JT, UK.ORCID https://orcid.org/0000-0001-6168-0060
Florian KopfThe Hamburg Centre for Ultrafast Imaging, Universität Hamburg, Hamburg, Germany.
Frank SobottSchool of Molecular and Cellular Biology, University of Leeds, Leeds LS2 9JT, UK.ORCID https://orcid.org/0000-0001-9029-1865
Diana C F MonteiroThe Hamburg Centre for Ultrafast Imaging, Universität Hamburg, Hamburg, Germany.ORCID https://orcid.org/0000-0002-6318-7306
Martin TrebbinDepartment of Chemistry,State University of New York at Buffalo, New York, USA.ORCID https://orcid.org/0000-0001-8278-5865
Stephen P MuenchSchool of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, UK.ORCID https://orcid.org/0000-0001-6869-4414
Howard D WhiteDepartment of Physiological Sciences, Eastern Virginia Medical School, Norfolk, Virginia USA.ORCID https://orcid.org/0000-0003-1066-2051

Funding

Medical Research Council MR/P018491/1Wellcome Trust
6 · The paper itself

Abstract

Structural biology generally provides static snapshots of protein conformations that can provide information on the functional mechanisms of biological systems. Time-resolved structural biology provides a means to visualize, at near-atomic resolution, the dynamic conformational changes that macromolecules undergo as they function. X-ray free-electron-laser technology has provided a powerful tool to study enzyme mechanisms at atomic resolution, typically in the femtosecond to picosecond timeframe. Complementary to this, recent advances in the resolution obtainable by electron microscopy and the broad range of samples that can be studied make it ideally suited to time-resolved approaches in the microsecond to millisecond timeframe to study large loop and domain motions in biomolecules. Here we describe a cryo-EM grid preparation device that permits rapid mixing, voltage-assisted spraying and vitrification of samples. It is shown that the device produces grids of sufficient ice quality to enable data collection from single grids that results in a sub-4 Å reconstruction. Rapid mixing can be achieved by blot-and-spray or mix-and-spray approaches with a delay of ∼10 ms, providing greater temporal resolution than previously reported mix-and-spray approaches.

Indexed as

microscope hardwaresample preparationstructural biologytime-resolved cryo-EMvoltage-assisted spraying

Identifiers

PMID31709058
PMCPMC6830222

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LicenceCC BY
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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.