Damage before destruction? X-ray-induced changes in single-pulse serial femtosecond crystallography

Serial femtosecond crystallography (SFX) exploits extremely brief X-ray free-electron laser pulses to obtain diffraction data before destruction of the crystal. However, during the pulse X-ray-induced site-specific radiation damage can occur, leading to electronic state and/or structural changes. Here, we present a systematic exploration of the effect of single-pulse duration and energy (and consequently different dose rates) on site-specific radiation damage under typical SFX room-temperature experimental conditions. For the first time in SFX we directly measured the photon pulse duration, varying from less than 10 fs to more than 50 fs, and used three pulse energies to probe in-pulse damage in two radiation-sensitive proteins: the iron-heme peroxidase DtpAa and the disulfide-rich thaumatin. While difference-map features arising from radiation damage are observed, they do not lead to significant change in refined atomic coordinates or key bond lengths. Our work thus provides experimental verification that average atomic coordinates are not significantly perturbed by radiation damage in typical SFX experiments.

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Publication Details

Journal
IUCrJ
Published
2025-04-14
DOI
https://doi.org/10.1107/s2052252525002660
Citations
5
Primary Topic
Enzyme Structure and Function
Type
article
Field-Weighted Citation Impact
2.59
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article

Damage before destruction? X-ray-induced changes in single-pulse serial femtosecond crystallography

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5 citations
IUCrJ
Enzyme Structure and Function
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article

Damage before destruction? X-ray-induced changes in single-pulse serial femtosecond crystallography

D. Voulot, Amy J. Thompson, Martin V. Appleby, Eduard Prat, Bill Pedrini, Chia‐Ying Huang, Nicole Hiller, Philipp Dijkstal, Jonathan A. R. Worrall, Michael A. Hough, Greta Aßmann, Robin Leslie Owen, John H. Beale, Florian Dworkowski, Samuel Perrett, Thomas J. Mason, L.J. Williams
article en
5 citations

Abstract

Serial femtosecond crystallography (SFX) exploits extremely brief X-ray free-electron laser pulses to obtain diffraction data before destruction of the crystal. However, during the pulse X-ray-induced site-specific radiation damage can occur, leading to electronic state and/or structural changes. Here, we present a systematic exploration of the effect of single-pulse duration and energy (and consequently different dose rates) on site-specific radiation damage under typical SFX room-temperature experimental conditions. For the first time in SFX we directly measured the photon pulse duration, varying from less than 10 fs to more than 50 fs, and used three pulse energies to probe in-pulse damage in two radiation-sensitive proteins: the iron-heme peroxidase DtpAa and the disulfide-rich thaumatin. While difference-map features arising from radiation damage are observed, they do not lead to significant change in refined atomic coordinates or key bond lengths. Our work thus provides experimental verification that average atomic coordinates are not significantly perturbed by radiation damage in typical SFX experiments.

IUCrJVol. 12(3)
University of Essex (GB), Paul Scherrer Institute (CH), Diamond Light Source (GB), Imperial College London (GB)
Openalex Percentile: Top 11%
Enzyme Structure and Function
2.59
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