| Literature DB >> 27175373 |
Sebastian Matthias Markert1, Sebastian Britz1, Sven Proppert2, Marietta Lang1, Daniel Witvliet3, Ben Mulcahy3, Markus Sauer4, Mei Zhen3, Jean-Louis Bessereau5, Christian Stigloher1.
Abstract
Correlating molecular labeling at the ultrastructural level with high confidence remains challenging. Array tomography (AT) allows for a combination of fluorescence and electron microscopy (EM) to visualize subcellular protein localization on serial EM sections. Here, we describe an application for AT that combines near-native tissue preservation via high-pressure freezing and freeze substitution with super-resolution light microscopy and high-resolution scanning electron microscopy (SEM) analysis on the same section. We established protocols that combine SEM with structured illumination microscopy (SIM) and direct stochastic optical reconstruction microscopy (dSTORM). We devised a method for easy, precise, and unbiased correlation of EM images and super-resolution imaging data using endogenous cellular landmarks and freely available image processing software. We demonstrate that these methods allow us to identify and label gap junctions in Caenorhabditis elegans with precision and confidence, and imaging of even smaller structures is feasible. With the emergence of connectomics, these methods will allow us to fill in the gap-acquiring the correlated ultrastructural and molecular identity of electrical synapses.Entities:
Keywords: Caenorhabditis elegans; correlative light and electron microscopy; direct stochastic optical reconstruction microscopy; gap junction; structured illumination microscopy; super-resolution microscopy
Year: 2016 PMID: 27175373 PMCID: PMC4855082 DOI: 10.1117/1.NPh.3.4.041802
Source DB: PubMed Journal: Neurophotonics ISSN: 2329-423X Impact factor: 3.593