Filling the gap: adding super-resolution to array tomography for correlated ultrastructural and molecular identification of electrical synapses at the C. elegans connectome

被引:28
|
作者
Markert, Sebastian Matthias [1 ]
Britz, Sebastian [1 ]
Proppert, Sven [2 ,3 ]
Lang, Marietta [1 ]
Witvliet, Daniel [4 ,5 ,6 ]
Mulcahy, Ben [4 ,5 ,6 ]
Sauer, Markus [2 ]
Zhen, Mei [4 ,5 ,6 ]
Bessereau, Jean-Louis [7 ]
Stigloher, Christian [1 ]
机构
[1] Univ Wurzburg, Bioctr, Div Electron Microscopy, Hubland, D-97074 Wurzburg, Germany
[2] Univ Wurzburg, Dept Biotechnol & Biophys, Hubland, D-97074 Wurzburg, Germany
[3] Univ Wurzburg, Dept Neurophysiol, Inst Physiol, Rontgenring 9, D-97070 Wurzburg, Germany
[4] Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, 600 Univ Ave, Toronto, ON M5G 1X5, Canada
[5] Univ Toronto, Dept Mol Genet, Physiol, 1 Kings Coll Cir, Toronto, ON M5S 1A8, Canada
[6] Univ Toronto, Inst Med Sci, 1 Kings Coll Cir, Toronto, ON M5S 1A8, Canada
[7] Univ Lyon 1, Inst NeuroMyoGene, CNRS UMR 5310, INSERM U1217, 16 Rue R Dubois, F-69622 Villeurbanne, France
基金
加拿大健康研究院;
关键词
Caenorhabditis elegans; super-resolution microscopy; direct stochastic optical reconstruction microscopy; structured illumination microscopy; correlative light and electron microscopy; gap junction; RESOLUTION LIMIT; MICROSCOPY; FLUORESCENCE; INNEXINS; RECONSTRUCTION; FAMILY;
D O I
10.1117/1.NPh.3.4.041802
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (C) The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
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页数:10
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