Limiting the effects of radiation damage in MicroED through dose selection during data processing

Microcrystal electron diffraction (MicroED), also known as three-dimensional electron diffraction (3D ED), allows the collection of diffraction data from submicrometre-sized crystals under low electron-dose conditions. Despite having several advantages over conventional X-ray crystallographic techniques, susceptibility to radiation damage is a great challenge that remains to be solved in MicroED. Similar to X-ray crystallography, radiation damage to the macromolecular crystal structures in MicroED manifests in two forms: global damage that affects the overall order of the crystal lattice and site-specific damage that affects highly sensitive residues and moieties in macromolecules. Traditionally, the unit e<sup>-</sup> Å<sup>-2</sup> has been used for electron-dose estimations, which does not consider the interaction between the incident electron beam and the sample. In this study, we clarify the terminology for describing `dose' in electron crystallography, including the procedure for converting values from e<sup>-</sup> Å<sup>-2</sup> to grays (Gy). Furthermore, we investigated data-processing strategies that could be used to limit the effects of radiation damage to the crystal. During MicroED data collection, radiation damage increases with the number of acquired ED frames because the accumulated electron dose increases. Data collected from several crystals and processed in this way can be merged to increase the completeness and subsequently be used for structure refinement. According to our results, this approach improves the resolution of the data, the data statistics, the structure determination and the quality of the final structure.

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Publication Details

Journal
Acta Crystallographica Section D Structural Biology
Published
2025-11-06
DOI
https://doi.org/10.1107/s205979832500912x
Citations
1
Primary Topic
Enzyme Structure and Function
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article
Field-Weighted Citation Impact
0.52
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article

Limiting the effects of radiation damage in MicroED through dose selection during data processing

Hongyi Xu, Uwe H. Sauer, Jingjing Zhao, Gerhard Höfer et al.
1 citations
Acta Crystallographica Section D Structural Biology
Enzyme Structure and Function
0.52
article

Limiting the effects of radiation damage in MicroED through dose selection during data processing

Hongyi Xu, Uwe H. Sauer, Jingjing Zhao, Gerhard Höfer, Henri Colyn Bwanika
article en
1 citations

Abstract

Microcrystal electron diffraction (MicroED), also known as three-dimensional electron diffraction (3D ED), allows the collection of diffraction data from submicrometre-sized crystals under low electron-dose conditions. Despite having several advantages over conventional X-ray crystallographic techniques, susceptibility to radiation damage is a great challenge that remains to be solved in MicroED. Similar to X-ray crystallography, radiation damage to the macromolecular crystal structures in MicroED manifests in two forms: global damage that affects the overall order of the crystal lattice and site-specific damage that affects highly sensitive residues and moieties in macromolecules. Traditionally, the unit e<sup>-</sup> Å<sup>-2</sup> has been used for electron-dose estimations, which does not consider the interaction between the incident electron beam and the sample. In this study, we clarify the terminology for describing `dose' in electron crystallography, including the procedure for converting values from e<sup>-</sup> Å<sup>-2</sup> to grays (Gy). Furthermore, we investigated data-processing strategies that could be used to limit the effects of radiation damage to the crystal. During MicroED data collection, radiation damage increases with the number of acquired ED frames because the accumulated electron dose increases. Data collected from several crystals and processed in this way can be merged to increase the completeness and subsequently be used for structure refinement. According to our results, this approach improves the resolution of the data, the data statistics, the structure determination and the quality of the final structure.

Acta Crystallographica Section D Structural BiologyVol. 81(12)
Australian National University (AU), Stockholm University (SE), Umeå University (SE)
Openalex Percentile: Top 30%
Enzyme Structure and Function
0.52
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