Abstract
Since scanning transmission electron microscopy can produce high signal-to-noise ratio bright-field images of thick (≥500. nm) specimens, this tool is emerging as the method of choice to study thick biological samples via tomographic approaches. However, in a convergent-beam configuration, the depth of field is limited because only a thin portion of the specimen (from a few nanometres to tens of nanometres depending on the convergence angle) can be imaged in focus. A method known as through-focal imaging enables recovery of the full depth of information by combining images acquired at different levels of focus. In this work, we compare tomographic reconstruction with the through-focal tilt-series approach (a multifocal series of images per tilt angle) with reconstruction with the classic tilt-series acquisition scheme (one single-focus image per tilt angle). We visualised the base of the flagellum in the protist Trypanosoma brucei via an acquisition and image-processing method tailored to obtain quantitative and qualitative descriptors of reconstruction volumes. Reconstructions using through-focal imaging contained more contrast and more details for thick (≥500. nm) biological samples.
| Original language | English |
|---|---|
| Pages (from-to) | 9-15 |
| Number of pages | 7 |
| Journal | Micron |
| Volume | 77 |
| DOIs | |
| Publication status | Published - 1 Oct 2015 |
| Externally published | Yes |
Keywords
- Depth of field
- Flagella
- Scanning transmission electron microscopy
- Through-focal tilt-series
- Tomography
- Transmission electron microscopy
- Trypanosome
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