bioRxivCell BiologyPreprint
Bridging the resolution gap in cryo-CLEM by introducing cryo-SXT: cryo-CLXEM
Johannes Groen, Anastasia D. GaziiD, Sergey KapishnikoviD, Anne BrelotiD, Matthijn R. J. VosiD, Jost EnningaiD, Eva PereiroiD, Anna Sartori-RuppiD
Abstract
Cryo-imaging in cellular biology provides the means to visualize the cellular interieur at close-to-native conditions. A cornerstone in the field has been cryo-correlative light and electron microscopy (cryo-CLEM), with cryo-visible light fluorescent microscopy (cryo-VLFM) providing the specificity by tagging macromolecules or structures and cryo-electron tomography (cryo-ET) for the structural details at molecular level. The large resolution gap between these techniques, however, is limiting this correlative workflow as cryo-ET targets are often smaller than the resolution limit of cryo-VLFM. Here we introduce cryo-soft X-ray tomography (cryo-SXT) as an intermediate step that can compensate for the partial view and limited resolution of cryo-VLFM by providing invaluable cellular context information in 3D to the cryo-ET dataset within an integrated workflow.
- assay: imaging
- assay: cryo-EM
- research focus: cell type annotation
- research focus: spatial domain detection
- approach: experimental assay
- Citations
- 1
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