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Brink, M. C.

Publications and source records attributed to Brink, M. C..

2 recordsLinked to original sources

SXTractor: A Self-Supervised Feature Extractor of Soft X-Ray Images That Enables Few-Shot Tomogram Segmentation

Soft X-ray tomography (SXT) is a powerful, non-invasive bio-imaging technique that enables visualization of cellular structures in near-native states. Despite its potential, the development of dedicated image analysis tools -- particularly deep-learning-based models -- has been limited, largely due to the limited accessibility of soft X-ray microscopes and the scarcity of labeled SXT data. To address this deficit, in this work, we present SXTractor, a self-supervised SXT feature extractor based on the DINO framework. SXTractor can be fine-tuned with minimal labeled data and effectively adapted to various downstream tasks. We demonstrate its utility on few-shot tomogram segmentation, where it significantly outperforms the model when trained from scratch. Furthermore, it achieves few-shot segmentation performance comparable to that of the Segment Anything Model (SAM), despite SAM being a segmentation-specific model pretrained on millions of labeled images with a significantly larger model size. Most importantly, SXTractor enables a diverse range of downstream applications of deep learning to SXT, thus offering a practical and scalable solution for SXT image analysis in data-constrained settings.

bioengineering↗

Demonstrating Soft X-Ray Tomography in the lab for correlative cryogenic biological imaging using X-rays and light microscopy

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.

biophysics↗