Literature DB >> 31326595

Multiplexed expansion microscopy of the brain through fluorophore screening.

Kyeongbae Min1, In Cho1, Myunghwan Choi1, Jae-Byum Chang2.   

Abstract

Super-resolution microscopy techniques have been widely adopted in biological sciences. Recently, a new super-resolution microscopy technique, called expansion microscopy (ExM) has been developed. In this technique, biomolecules inside specimens are first labeled with fluorophores, followed by in-situ hydrogel synthesis and physical expansion of the specimens. Image quality, including brightness and signal-to-noise ratio, depends on the extent to which fluorophores have bleached during the in-situ hydrogel synthesis process. In this work, we compared the fluorescence signal brightness of more than 20 fluorophores, after expansion, to identify the best fluorophore set for 4-color expansion microscopy imaging. In addition, we achieved 5-color multiplexed expansion microscopy by photo-bleaching one of the four fluorophores and re-staining thereafter.
Copyright © 2019 Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 31326595     DOI: 10.1016/j.ymeth.2019.07.017

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  3 in total

1.  Expansion Microscopy: Toward Nanoscale Imaging of a Diverse Range of Biomolecules.

Authors:  Aleksandra Klimas; Yongxin Zhao
Journal:  ACS Nano       Date:  2020-07-06       Impact factor: 15.881

2.  Protein-retention expansion microscopy for visualizing subcellular organelles in fixed brain tissue.

Authors:  Logan A Campbell; Katy E Pannoni; Niesha A Savory; Dinesh Lal; Shannon Farris
Journal:  J Neurosci Methods       Date:  2021-07-07       Impact factor: 2.987

Review 3.  Expansion microscopy: A powerful nanoscale imaging tool for neuroscientists.

Authors:  Brendan R Gallagher; Yongxin Zhao
Journal:  Neurobiol Dis       Date:  2021-04-02       Impact factor: 5.996

  3 in total

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