Structural Biology, Rosalind Franklin Institute, Didcot, United Kingdom
Thomas Glen
Structural Biology, Rosalind Franklin Institute, Didcot, United Kingdom
Jake LR Smith
Structural Biology, Rosalind Franklin Institute, Didcot, United Kingdom; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
Elaine ML Ho
Artificial Intelligence and Informatics, Rosalind Franklin Institute, Didcot, United Kingdom
Luis MA Perdigão
Artificial Intelligence and Informatics, Rosalind Franklin Institute, Didcot, United Kingdom
Structural Biology, Rosalind Franklin Institute, Didcot, United Kingdom; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom; Diamond Light Source, Harwell Science & Innovation Campus, Didcot, United Kingdom
Ron Kelley
Materials and Structural Analysis Division, Thermo Fisher Scientific, Eindhoven, Netherlands
Research Group Cryo-EM Technology, Max Planck Institute of Biochemistry, Martinsried, Germany
Liang Wu
Structural Biology, Rosalind Franklin Institute, Didcot, United Kingdom; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
Artificial Intelligence and Informatics, Rosalind Franklin Institute, Didcot, United Kingdom
James H Naismith
Structural Biology, Rosalind Franklin Institute, Didcot, United Kingdom; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
Structural Biology, Rosalind Franklin Institute, Didcot, United Kingdom; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom
Serial focussed ion beam scanning electron microscopy (FIB/SEM) enables imaging and assessment of subcellular structures on the mesoscale (10 nm to 10 µm). When applied to vitrified samples, serial FIB/SEM is also a means to target specific structures in cells and tissues while maintaining constituents’ hydration shells for in situ structural biology downstream. However, the application of serial FIB/SEM imaging of non-stained cryogenic biological samples is limited due to low contrast, curtaining, and charging artefacts. We address these challenges using a cryogenic plasma FIB/SEM. We evaluated the choice of plasma ion source and imaging regimes to produce high-quality SEM images of a range of different biological samples. Using an automated workflow we produced three-dimensional volumes of bacteria, human cells, and tissue, and calculated estimates for their resolution, typically achieving 20–50 nm. Additionally, a tag-free localisation tool for regions of interest is needed to drive the application of in situ structural biology towards tissue. The combination of serial FIB/SEM with plasma-based ion sources promises a framework for targeting specific features in bulk-frozen samples (>100 µm) to produce lamellae for cryogenic electron tomography.