Related Experiment Video
Updated: Mar 2, 2026

Correlative Light Electron Microscopy CLEM for Tracking and Imaging Viral Protein Associated Structures in Cryo-immobilized Cells
Published on: September 7, 2018
triCLEM: Combining high-precision, room temperature CLEM with cryo-fluorescence microscopy to identify very rare
Nicholas R Ader1, Wanda Kukulski2
1MRC Laboratory of Molecular Biology, Cambridge, United Kingdom; National Institutes of Health, Bethesda, MD, United States.
Abstract:
Fiducial-based correlation of fluorescence and electron microscopy data from high-pressure frozen and resin-embedded samples allows for high-precision localization of fluorescent signals to subcellular ultrastructure. Here we introduce the triCLEM procedure to facilitate the identification of very rare events for high-precision correlation. We present a detailed protocol to screen high-pressure frozen cell monolayers on sapphire disks for very rare signals by cryo-fluorescence microscopy, relocate the cells of interest after freeze substitution and Lowicryl embedding, and perform fiducial-based correlation of the identified fluorescent signals to high-magnification electron tomograms. We show the applicability of the protocol to localize and image damaged mitochondria marked by the presence of Parkin, a protein involved in initiating mitophagy. We discuss how this extension to previously published fiducial-based correlation procedures has potential to both allow identifying very rare events and assess the quality of preservation in high-pressure frozen samples.
Related Concept Videos
Cryo-electron Microscopy
Super-resolution Fluorescence Microscopy

