Impact of gas background on XFEL single-particle imaging

Single-particle imaging (SPI) using X-ray free-electron Lasers (XFELs) offers the potential to determine protein structures at high spatial and temporal resolutions without the need for crystallization or vitrification. However, the technique faces challenges due to weak diffraction signals from single proteins and significant background scattering from gases used for sample delivery. A recent observation of a diffraction pattern from an isolated GroEL protein complex Ekeberg T et al. (Light Sci Appl 13:15, 2024. https://doi.org/10.1038/274s41377-023-01352-7 ) had similar numbers of signal and background photons. Ongoing efforts aim to reduce the background created by sample delivery, with one approach replacing most of the used gas with helium Yenupuri T et al. (Sci Rep 14:4401, 2024. https://doi.org/10.1038/s41598-024-54605-9 ). In this study, we investigate the effects of a reduced background on the resolution limits for SPI of isolated proteins under different experiment conditions. As a test case, we used GroEL, and we used experimentally derived parameters for our simulations. We observe that background significantly impacts the achievable resolution, particularly when the signal strength is comparable to the background. This is best exemplified at 6.0 keV, where a background reduction by a factor of 10 leads to a resolution improvement from 1.9 to 1.2 nm, for a dataset of [Formula: see text] patterns.

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Journal
Scientific Reports
Published
2025-08-12
DOI
https://doi.org/10.1038/s41598-025-15092-8
Primary Topic
Advanced X-ray Imaging Techniques
Type
article
Field-Weighted Citation Impact
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article

Impact of gas background on XFEL single-particle imaging

Johan Bielecki, Filipe R. N. C. Maia, Tong You
Scientific Reports
Advanced X-ray Imaging Techniques
article

Impact of gas background on XFEL single-particle imaging

Johan Bielecki, Filipe R. N. C. Maia, Tong You
article en

Abstract

Single-particle imaging (SPI) using X-ray free-electron Lasers (XFELs) offers the potential to determine protein structures at high spatial and temporal resolutions without the need for crystallization or vitrification. However, the technique faces challenges due to weak diffraction signals from single proteins and significant background scattering from gases used for sample delivery. A recent observation of a diffraction pattern from an isolated GroEL protein complex Ekeberg T et al. (Light Sci Appl 13:15, 2024. https://doi.org/10.1038/274s41377-023-01352-7 ) had similar numbers of signal and background photons. Ongoing efforts aim to reduce the background created by sample delivery, with one approach replacing most of the used gas with helium Yenupuri T et al. (Sci Rep 14:4401, 2024. https://doi.org/10.1038/s41598-024-54605-9 ). In this study, we investigate the effects of a reduced background on the resolution limits for SPI of isolated proteins under different experiment conditions. As a test case, we used GroEL, and we used experimentally derived parameters for our simulations. We observe that background significantly impacts the achievable resolution, particularly when the signal strength is comparable to the background. This is best exemplified at 6.0 keV, where a background reduction by a factor of 10 leads to a resolution improvement from 1.9 to 1.2 nm, for a dataset of [Formula: see text] patterns.

Scientific ReportsVol. 15(1)
Science for Life Laboratory (SE), European X-Ray Free-Electron Laser (DE)
Vetenskapsrådet, Uppsala Universitet
Openalex Percentile: Top 73%
Advanced X-ray Imaging Techniques
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