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.
Cryo-plasma FIB/SEM volume imaging of biological specimens.
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作者:Dumoux Maud, Glen Thomas, Smith Jake L R, Ho Elaine M L, Perdigão Luis M A, Pennington Avery, Klumpe Sven, Yee Neville B Y, Farmer David Andrew, Lai Pui Y A, Bowles William, Kelley Ron, Plitzko Jürgen M, Wu Liang, Basham Mark, Clare Daniel K, Siebert C Alistair, Darrow Michele C, Naismith James H, Grange Michael
| 期刊: | Elife | 影响因子: | 6.400 |
| 时间: | 2023 | 起止号: | 2023 Feb 21; 12:e83623 |
| doi: | 10.7554/eLife.83623 | ||
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