Scientific ReportsBiophysicsPeer-reviewed journal article
Demonstrating Soft X-Ray Tomography in the lab for correlative cryogenic biological imaging using X-rays and light microscopy
Stephen J. M. O'ConnoriD, David Rogers, Maryna Kobylynska, James A. GeraetsiD, Katja ThayseniD, Jacob Marcus EgebjergiD, Madeleen C. BrinkiD, Louisa HerbslebiD, Michaela SalákováiD, Leon Fuchs, Frauke AlvesiD, Claus FeldmanniD, Axel A. EkmaniD, Paul J. SheridaniD, William Fyans, Tony McEnroe, Fergal O’ReillyiD, Kenneth FahyiD, Roland A. FleckiD, Daniel WüstneriD, Jeremy C. SimpsoniD, Andreas WalteriD, Sergey KapishnikoviD
Abstract
Soft X-ray tomography (SXT) enables native-contrast three-dimensional (3D) imaging of fully hydrated, cryogenically preserved biological samples, revealing ultrastructural details without the need for staining, embedding, or sectioning. Traditionally available only at synchrotron facilities, recent advances in laser-driven plasma sources have led to the development of compact soft X-ray microscopes, such as the SXT-100. The SXT-100 achieves imaging resolutions down to 54 nm full-pitch, with tomograms acquired in 30 minutes to two hours. Integrated with an epifluorescence microscope, the SXT-100 facilitates correlative workflows by bridging fluorescence and electron microscopy while preserving the structural integrity of vitrified samples. We demonstrate the capabilities of the SXT-100 through various use cases, including imaging Euglena gracilis, Saccharomyces cerevisiae yeast cells, and nanoparticles in mammalian cells. The relatively short tomogram acquisition times, the virtually non-destructive nature of soft X-ray tomography, and its quantitative imaging capabilities underscore its potential as a powerful tool for advanced biological imaging. Future developments promise enhanced throughput and deeper integration with emerging correlative imaging modalities, and a wider variety of sample types including tissue.
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