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Issue 37, 2018
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Expansion enhanced nanoscopy

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Abstract

The advance of optical super-resolution fluorescence microscopy has revolutionized our vision of the subcellular world. Further improvement in the spatial resolution is of great significance for structural and functional investigations. The recently developed expansion microscopy (ExM), which achieves sub-diffraction imaging via physical expansion of the sample, provides a great opportunity for further resolution enhancement of existing optical super-resolution techniques. However, although such combination seems apparent, several technical obstacles, especially the dramatic loss of fluorescence signal during ExM sample preparation, have hampered this goal. In this work, aiming at this challenge, we have developed new strategies to retain and increase the fluorescence of the expanded sample. With the new labeling methods, we have successfully made the labeling density of expanded samples sufficing the Nyquist sampling criteria for optical super-resolution imaging, such as stimulated emission depletion microscopy (STED) and super-resolution optical fluctuation imaging (SOFI). The newly developed expansion nanoscopic imaging (ExN) approaches, i.e. ExSTED and ExSOFI, demonstrated up to 4-fold resolution enhancement compared to standard STED and SOFI, providing a simple and effective way to realize high resolution imaging both at the cellular and tissue level.

Graphical abstract: Expansion enhanced nanoscopy

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Publication details

The article was received on 26 May 2018, accepted on 09 Sep 2018 and first published on 12 Sep 2018


Article type: Communication
DOI: 10.1039/C8NR04267E
Citation: Nanoscale, 2018,10, 17552-17556
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    Expansion enhanced nanoscopy

    R. Li, X. Chen, Z. Lin, Y. Wang and Y. Sun, Nanoscale, 2018, 10, 17552
    DOI: 10.1039/C8NR04267E

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