Scanning Switch-off Microscopy for Super-Resolution Fluorescence Imaging

Super-resolution (SR) microscopy provides a revolutionary optical imaging approach by breaking the diffraction limit of light, while the commonly required special instrumentation with complex optical setup hampers its popularity. Here, we present a scanning switch-off microscopy (SSM) concept that exploits the omnipresent switch-off response of fluorophores to enable super-resolution imaging using a commercial confocal microscope. We validated the SSM model with theoretical calculations and experiments. An imaging resolution of ∼100 nm was obtained for DNA origami nanostructures and cellular cytoskeletons using fluorescent labels of Alexa 405, Alexa 488, Cy3, and Atto 488. Notably, super-resolution imaging of live cells was realized with SSM, by employing a dronpa fluorescent protein as the fluorescent label. In principle, this SSM method can be applied to any excitation laser scanning-based microscope.

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Publication Details

Journal
Nano Letters
Published
2024-09-19
DOI
https://doi.org/10.1021/acs.nanolett.4c02452
Citations
6
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
3.97

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article

Scanning Switch-off Microscopy for Super-Resolution Fluorescence Imaging

Chunhai Fan, Zhaoshuai Gao, Suhui Deng, Shangguo Hou et al.
6 citations
Nano Letters
Advanced Fluorescence Microscopy Techniques
3.97
article

Scanning Switch-off Microscopy for Super-Resolution Fluorescence Imaging

Chunhai Fan, Zhaoshuai Gao, Suhui Deng, Shangguo Hou, Le Liang, Bin Kang, Weina Fang, Qian Li, Fei Wang, Linjie Guo, Hong‐Yuan Chen
article en
6 citations

Abstract

Super-resolution (SR) microscopy provides a revolutionary optical imaging approach by breaking the diffraction limit of light, while the commonly required special instrumentation with complex optical setup hampers its popularity. Here, we present a scanning switch-off microscopy (SSM) concept that exploits the omnipresent switch-off response of fluorophores to enable super-resolution imaging using a commercial confocal microscope. We validated the SSM model with theoretical calculations and experiments. An imaging resolution of ∼100 nm was obtained for DNA origami nanostructures and cellular cytoskeletons using fluorescent labels of Alexa 405, Alexa 488, Cy3, and Atto 488. Notably, super-resolution imaging of live cells was realized with SSM, by employing a dronpa fluorescent protein as the fluorescent label. In principle, this SSM method can be applied to any excitation laser scanning-based microscope.

Nano LettersVol. 24(39)
Nanchang University (CN), Shanghai Jiao Tong University (CN), Chinese Academy of Sciences (CN), Wuhan University (CN), Shenzhen Bay Laboratory (CN), Shanghai Institute of Applied Physics (CN), Nanjing University (CN)
National Natural Science Foundation of China, Science and Technology Commission of Shanghai Municipality, Nanchang University, National Key Research and Development Program of China
Affordable and clean energy
Openalex Percentile: Top 7%
Advanced Fluorescence Microscopy Techniques
3.97
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