1. Precision in situ cryogenic correlative light and electron microscopy of optogenetically positioned organelles.
- Author
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Tillu VA, Redpath GMI, Rae J, Ruan J, Yao Y, Cagigas ML, Whan R, Hardeman EC, Gunning PW, Ananthanarayanan V, Parton RG, and Ariotti N
- Subjects
- Electron Microscope Tomography methods, Humans, Microscopy, Fluorescence methods, Cryoelectron Microscopy methods, Organelles ultrastructure, Optogenetics methods
- Abstract
Unambiguous targeting of cellular structures for in situ cryo-electron microscopy in the heterogeneous, dense and compacted environment of the cytoplasm remains challenging. Here, we have developed a cryogenic correlative light and electron microscopy (cryo-CLEM) workflow that utilizes thin cells grown on a mechanically defined substratum for rapid analysis of organelles and macromolecular complexes by cryo-electron tomography (cryo-ET). We coupled these advancements with optogenetics to redistribute perinuclear-localised organelles to the cell periphery, allowing visualisation of organelles that would otherwise be positioned in cellular regions too thick for cryo-ET. This reliable and robust workflow allows for fast in situ analyses without the requirement for cryo-focused ion beam milling. Using this protocol, cells can be frozen, imaged by cryo-fluorescence microscopy and be ready for batch cryo-ET within a day., Competing Interests: Competing interests The authors declare no competing or financial interests., (© 2024. Published by The Company of Biologists Ltd.)
- Published
- 2024
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