Non-linear scanning switch-off microscopy for super-resolution fluorescence imaging

Author:

Gao Zhaoshuai1,Hou Shangguo2,Deng Suhui3,Liang Le4,Wang Fei5ORCID,Guo Linjie6,Fang Weina6,Li Qian1ORCID,Kang Bin7ORCID,Chen Hong-Yuan8ORCID,Fan Chunhai1ORCID

Affiliation:

1. Shanghai Jiao Tong University

2. Shenzhen Bay Laboratory

3. Nanchang University

4. Wuhan University

5. sjtu

6. Chinese Academy of Sciences

7. Nanjing University

8. Nangjing University

Abstract

Abstract Super-resolution (SR) microscopy provides a revolutionary approach to study cells and animals by breaking the diffraction limit of optical imaging. However, the popularity of the super-resolution microscope in biological sciences remains to be impeded by the high cost of hardware and/or the complexity of software. Here, we present a conceptually different non-linear scanning switch-off microscopy (nSSM) that exploits the omnipresent switch-off effect of fluorophores to enable super-resolution imaging beyond the diffraction limit. We develop a theoretical model of nSSM and experimentally implement the nSSM scheme with an unmodified confocal microscope. We also release a free code for the automatic reconstruction of super-resolution images. By measuring the PSF of the imaged DNA origami nanostructure and mammalian cytoskeleton structures, we demonstrate an SR resolution of ~ 100 nm that excels the optical resolution limit by over two folds. We further show the generality of nSSM using a range of commercially available fluorescent dyes and proteins to realize SR imaging in various settings. This nSSM methodology may in principle empower any confocal microscope to implement SR imaging to promote biological research.

Publisher

Research Square Platform LLC

Reference37 articles.

1. Fluorescence nanoscopy in cell biology;Sahl SJ;Nat. Rev. Mol. Cell Biol.,2017

2. Visualizing and discovering cellular structures with super-resolution microscopy;Sigal Yaron M;Science,2018

3. Super-resolution microscopy demystified;Schermelleh L;Nat. Cell Biol.,2019

4. Confocal optical microscopy;Webb RH;Rep. Prog. Phys.,1996

5. Multiview confocal super-resolution microscopy;Wu Y;Nature,2021

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3