eLife (Feb 2023)

Cryo-plasma FIB/SEM volume imaging of biological specimens

  • Maud Dumoux,
  • Thomas Glen,
  • Jake LR Smith,
  • Elaine ML Ho,
  • Luis MA Perdigão,
  • Avery Pennington,
  • Sven Klumpe,
  • Neville BY Yee,
  • David Andrew Farmer,
  • Pui YA Lai,
  • William Bowles,
  • Ron Kelley,
  • Jürgen M Plitzko,
  • Liang Wu,
  • Mark Basham,
  • Daniel K Clare,
  • C Alistair Siebert,
  • Michele C Darrow,
  • James H Naismith,
  • Michael Grange

DOI
https://doi.org/10.7554/eLife.83623
Journal volume & issue
Vol. 12

Abstract

Read online

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.

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