Evidence map›Paper›PMID 41746258›Full record

ArticleActa crystallographica. Section D, Structural biology2026

Radiation-dose effects in correlative X-ray/cryo-electron microscopy of frozen-hydrated biological samples.

Thorsten B Blum, Vincent Olieric, Ana Diaz, Takashi Ishikawa, Volodymyr M Korkhov

Abstract read
In one paragraph

Article in Acta crystallographica. Section D, Structural biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Electrons and X-rays for diffraction and imaging.Acta crystallographica. Section D, Structural biology · 2026
    Review
  2. Damage-limited resolution for X-ray and electron microscopy of organic specimens.Acta crystallographica. Section D, Structural biology · 2026
    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.

Thorsten B BlumPSI Center for Life Sciences, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland.ORCID 0000-0002-1615-1941
Vincent OliericPSI Center for Photon Science, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland.ORCID 0000-0002-0533-7222
Ana DiazPSI Center for Photon Science, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland.ORCID 0000-0003-0479-4752
Takashi IshikawaPSI Center for Life Sciences, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland.ORCID 0000-0002-1976-7477
Volodymyr M KorkhovPSI Center for Life Sciences, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland.ORCID 0000-0002-0962-9433

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In cryo-electron microscopy (cryo-EM), imaging of biological specimens is restricted by the limited field of view and by sample thickness. Hard X-ray imaging, with its ability to penetrate samples several tens of micrometres thick, offers a complementary approach for high-resolution visualization. A major concern is whether cryo-preserved samples can withstand the handling conditions at synchrotron facilities without excessive icing, and whether the radiation exposure during X-ray imaging compromises specimen integrity, thereby hindering subsequent attempts to achieve high-resolution 3D reconstructions via cryo-EM. To evaluate this, we deposited apoferritin samples on a cryo-EM grid, exposed them to varied X-ray doses typical for X-ray tomography experiments at a synchrotron facility, and subsequently analysed the exposed particles by cryo-EM. Despite the apparent damage sustained throughout the experiment, the samples remained amenable to cryo-EM analysis, with structural details at a resolution of ∼4 Å at the highest absorbed X-ray dose of 100 MGy. By comparison, a similar cryo-EM dataset of apoferritin particles that were not exposed to X-rays but were mounted on the same cryo-EM grid resulted in a 3D reconstruction at 3.17 Å resolution. Thus, while radiation damage may limit the high-resolution information in specimens processed by cryo-X-ray tomography, the cryo-preserved biological material exposed to these high X-ray doses can still be used for subsequent cryo-EM workflows aiming to obtain structural biology insights at intermediate to high resolution. These findings lay the groundwork for an integrated imaging workflow that combines X-ray and cryo-EM techniques to enable multiscale analysis of thick vitrified biological specimens.

Indexed as

ApoferritinsCryoelectron MicroscopyAnimalsFreezingImaging, Three-DimensionalRadiation DosageSynchrotronsTomography, X-RayX-RaysApoferritinscorrelative microscopycryo-electron microscopycryo-X-ray tomography

Identifiers

PMID41746258
PMCPMC12954863

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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.