Cryo-plasma FIB/SEM volume imaging of biological specimens

Author:

Dumoux Maud1ORCID,Glen Thomas1,Smith Jake LR12,Ho Elaine ML3,Perdigão Luis MA3,Pennington Avery4,Klumpe Sven5,Yee Neville BY3ORCID,Farmer David Andrew4ORCID,Lai Pui YA4,Bowles William124ORCID,Kelley Ron6,Plitzko Jürgen M5ORCID,Wu Liang12,Basham Mark4ORCID,Clare Daniel K4,Siebert C Alistair4,Darrow Michele C3ORCID,Naismith James H12,Grange Michael12ORCID

Affiliation:

1. Structural Biology, Rosalind Franklin Institute

2. Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford

3. Artificial Intelligence and Informatics, Rosalind Franklin Institute

4. Diamond Light Source, Harwell Science & Innovation Campus

5. Research Group Cryo-EM Technology, Max Planck Institute of Biochemistry

6. Materials and Structural Analysis Division, Thermo Fisher Scientific

Abstract

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.

Funder

Wellcome Trust

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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