Correlative single‐molecule localization microscopy and electron tomography reveals endosome nanoscale domains. (11th July 2019)

• Record Type: Journal Article
• Authors: Franke, Christian; Repnik, Urska; Segeletz, Sandra; Brouilly, Nicolas; Kalaidzidis, Yannis; Verbavatz, Jean‐Marc; Zerial, Marino
• Is Part Of: Traffic. Volume 20:Number 8(2019)
• Page Start: 601
• Page End: 617
• Publication Date: 2019-07-11
• Subjects: electron tomography -- electron‐microscopy -- endosomes -- multicolor CLEM -- Rab5 -- single‐molecule localization microscopy -- super‐resolution microscopy -- Tokuyasu cryosectioning; Biological transport -- Periodicals; 571.6
• DOI: 10.1111/tra.12671
• Languages: English
• ISSNs: 1398-9219

Abstract

Abstract: Many cellular organelles, including endosomes, show compartmentalization into distinct functional domains, which, however, cannot be resolved by diffraction‐limited light microscopy. Single molecule localization microscopy (SMLM) offers nanoscale resolution but data interpretation is often inconclusive when the ultrastructural context is missing. Correlative light electron microscopy (CLEM) combining SMLM with electron microscopy (EM) enables correlation of functional subdomains of organelles in relation to their underlying ultrastructure at nanometer resolution. However, the specific demands for EM sample preparation and the requirements for fluorescent single‐molecule photo‐switching are opposed. Here, we developed a novel superCLEM workflow that combines triple‐color SMLM ( d STORM & PALM) and electron tomography using semi‐thin Tokuyasu thawed cryosections. We applied the superCLEM approach to directly visualize nanoscale compartmentalization of endosomes in HeLa cells. Internalized, fluorescently labeled Transferrin and EGF were resolved into morphologically distinct domains within the same endosome. We found that the small GTPase Rab5 is organized in nanodomains on the globular part of early endosomes. The simultaneous visualization of several proteins in functionally distinct endosomal sub‐compartments demonstrates the potential of superCLEM to link the ultrastructure of organelles with their molecular organization at nanoscale resolution. Abstract : Suborganelle compartmentalization cannot be resolved by diffraction‐limited light microscopy and interpreted without knowledge of the underlying ultrastructure. This work presents a novel superCLEM workflow that combines multicolor single‐molecule localization‐microscopy with electron tomography using semi‐thin Tokuyasu thawed cryosections to map fluorescent molecules on the ultrastructure of early endosomes. superCLEM reveals that the small GTPase Rab5 is organized in nanodomains largely devoid of cargo molecules Transferrin and EGF. This method opens new possibilities to perform structure‐function analysis of organelles at the nanoscale.