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Related Concept Videos

Cryo-electron Microscopy01:28

Cryo-electron Microscopy

4.6K
Conventional electron microscopy (EM) involves dehydration, fixation, and staining of biological samples, which distorts the native state of biological molecules and results in several artifacts. Also, the high-energy electron beam damages the sample and makes it difficult to obtain high-resolution images. These issues can be addressed using cryo-EM, which uses frozen samples and gentler electron beams. The technique was developed by Jacques Dubochet, Joachim Frank, and Richard Henderson, for...
4.6K

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Updated: Apr 18, 2026

Cryo-Structured Illumination Microscopic Data Collection from Cryogenically Preserved Cells
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A national facility for biological cryo-electron microscopy.

Helen R Saibil1, Kay Grünewald2, David I Stuart2

  • 1Crystallography, Institute for Structural and Molecular Biology, Birkbeck College, Malet Street, London WC1E 7HX, England.

Acta Crystallographica. Section D, Biological Crystallography
|January 24, 2015
PubMed
Summary

A new UK national facility will provide advanced three-dimensional electron microscopy (3D-EM) for structural biology research. This resource will offer state-of-the-art equipment and expert support for detailed molecular and cellular analysis.

Keywords:
three-dimensional electron microscopy

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Area of Science:

  • Structural Biology
  • Biophysics
  • Cell Biology

Background:

  • Three-dimensional electron microscopy (3D-EM) offers atomic-level insights into cellular machinery, disease mechanisms, and pathogen actions.
  • High-end 3D-EM research demands significant investment in equipment, infrastructure, and specialized expertise.

Purpose of the Study:

  • To outline plans for a UK national 3D-EM facility for integrated structural biology.
  • To enable world-leading research into the fundamental machinery of life.

Main Methods:

  • Establishment of a national facility with state-of-the-art equipment.
  • Provision of expert support for both single-particle analysis and cryo-tomography.
  • Integration with the Diamond Light Source for streamlined access and user-friendly workflows.

Main Results:

  • The facility will provide access to advanced 3D-EM capabilities.
  • It will support research at resolutions from atomic detail to the cellular context.
  • User-friendly workflows with near-real-time feedback will be developed.

Conclusions:

  • The proposed national facility will significantly advance structural biology research in the UK.
  • It will democratize access to cutting-edge 3D-EM technology.
  • The facility aims to foster internationally leading research in the machinery of life.