Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy

Polarization microscopy has been combined with single-molecule localization, but it’s often limited in either speed or resolution. Here the authors present polarized Structured Illumination Microscopy (pSIM), a method that uses polarized laser excitation to measure dye orientation during fast super-...

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Autores principales:	Karl Zhanghao, Xingye Chen, Wenhui Liu, Meiqi Li, Yiqiong Liu, Yiming Wang, Sha Luo, Xiao Wang, Chunyan Shan, Hao Xie, Juntao Gao, Xiaowei Chen, Dayong Jin, Xiangdong Li, Yan Zhang, Qionghai Dai, Peng Xi
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2019
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/080c2362f4c04472a1ce4e4338f97ada
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spelling	oai:doaj.org-article:080c2362f4c04472a1ce4e4338f97ada2021-12-02T16:58:27ZSuper-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy10.1038/s41467-019-12681-w2041-1723https://doaj.org/article/080c2362f4c04472a1ce4e4338f97ada2019-10-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-12681-whttps://doaj.org/toc/2041-1723Polarization microscopy has been combined with single-molecule localization, but it’s often limited in either speed or resolution. Here the authors present polarized Structured Illumination Microscopy (pSIM), a method that uses polarized laser excitation to measure dye orientation during fast super-resolution live cell imaging.Karl ZhanghaoXingye ChenWenhui LiuMeiqi LiYiqiong LiuYiming WangSha LuoXiao WangChunyan ShanHao XieJuntao GaoXiaowei ChenDayong JinXiangdong LiYan ZhangQionghai DaiPeng XiNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Karl Zhanghao Xingye Chen Wenhui Liu Meiqi Li Yiqiong Liu Yiming Wang Sha Luo Xiao Wang Chunyan Shan Hao Xie Juntao Gao Xiaowei Chen Dayong Jin Xiangdong Li Yan Zhang Qionghai Dai Peng Xi Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy
description	Polarization microscopy has been combined with single-molecule localization, but it’s often limited in either speed or resolution. Here the authors present polarized Structured Illumination Microscopy (pSIM), a method that uses polarized laser excitation to measure dye orientation during fast super-resolution live cell imaging.
format	article
author	Karl Zhanghao Xingye Chen Wenhui Liu Meiqi Li Yiqiong Liu Yiming Wang Sha Luo Xiao Wang Chunyan Shan Hao Xie Juntao Gao Xiaowei Chen Dayong Jin Xiangdong Li Yan Zhang Qionghai Dai Peng Xi
author_facet	Karl Zhanghao Xingye Chen Wenhui Liu Meiqi Li Yiqiong Liu Yiming Wang Sha Luo Xiao Wang Chunyan Shan Hao Xie Juntao Gao Xiaowei Chen Dayong Jin Xiangdong Li Yan Zhang Qionghai Dai Peng Xi
author_sort	Karl Zhanghao
title	Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy
title_short	Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy
title_full	Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy
title_fullStr	Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy
title_full_unstemmed	Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy
title_sort	super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy
publisher	Nature Portfolio
publishDate	2019
url	https://doaj.org/article/080c2362f4c04472a1ce4e4338f97ada
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Super-resolution imaging of fluorescent dipoles via polarized structured illumination microscopy

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