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Müller, A. ; Neukam, M. ; Ivanova, A. ; Sönmez, A. ; Münster, C. ; Kretschmar, S.* ; Kalaidzidis, Y.* ; Kurth, T.* ; Verbavatz, J.-M.* ; Solimena, M.

A global approach for quantitative super resolution and electron microscopy on cryo and epoxy sections using self-labeling protein tags.

Sci. Rep. 7:23 (2017)
Publ. Version/Full Text Research data DOI PMC
Open Access Gold
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Correlative light and electron microscopy (CLEM) is a powerful approach to investigate the molecular ultrastructure of labeled cell compartments. However, quantitative CLEM studies are rare, mainly due to small sample sizes and the sensitivity of fluorescent proteins to strong fixatives and contrasting reagents for EM. Here, we show that fusion of a self-labeling protein to insulin allows for the quantification of age-distinct insulin granule pools in pancreatic beta cells by a combination of super resolution and transmission electron microscopy on Tokuyasu cryosections. In contrast to fluorescent proteins like GFP organic dyes covalently bound to self-labeling proteins retain their fluorescence also in epoxy resin following high pressure freezing and freeze substitution, or remarkably even after strong chemical fixation. This enables for the assessment of age-defined granule morphology and degradation. Finally, we demonstrate that this CLEM protocol is highly versatile, being suitable for single and dual fluorescent labeling and detection of different proteins with optimal ultrastructure preservation and contrast.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Correlative Superresolution Fluorescence; Structured Illumination Microscopy; Pancreatic Beta-cells; Ultrathin Cryosections; Preferential Release; Plasma-membrane; Insulin-release; Fusion Proteins; Stored Insulin; Islet Cells
ISSN (print) / ISBN 2045-2322
e-ISSN 2045-2322
Quellenangaben Volume: 7, Issue: 1, Pages: , Article Number: 23 Supplement: ,
Publisher Nature Publishing Group
Publishing Place London
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute of Pancreatic Islet Research (IPI)