By developing a wide-field scheme for spectral measurement and implementing photoswitching, we synchronously obtained the fluorescence spectra and positions of ∼10 6 single molecules in labeled cells in minutes, which consequently enabled spectrally resolved, 'true-color' super-resolution microscopy. The method, called spectrally resolved stochastic optical reconstruction microscopy (SR-STORM), achieved cross-talk-free three-dimensional (3D) imaging for four dyes 10 nm apart in emission spectrum. Excellent resolution was obtained for every channel, and 3D localizations of all molecules were automatically aligned within one imaging path.
%0 Journal Article
%1 Zhang2015
%A Zhang, Zhengyang
%A Kenny, Samuel J.
%A Hauser, Margaret
%A Li, Wan
%A Xu, Ke
%D 2015
%J Nature Methods
%K 3D fluorescence high-throughput microscopy spectral_demixing superresolution
%N 10
%P 935--938
%R 10.1038/nmeth.3528
%T Ultrahigh-throughput single-molecule spectroscopy and spectrally resolved super-resolution microscopy
%V 12
%X By developing a wide-field scheme for spectral measurement and implementing photoswitching, we synchronously obtained the fluorescence spectra and positions of ∼10 6 single molecules in labeled cells in minutes, which consequently enabled spectrally resolved, 'true-color' super-resolution microscopy. The method, called spectrally resolved stochastic optical reconstruction microscopy (SR-STORM), achieved cross-talk-free three-dimensional (3D) imaging for four dyes 10 nm apart in emission spectrum. Excellent resolution was obtained for every channel, and 3D localizations of all molecules were automatically aligned within one imaging path.
@article{Zhang2015,
abstract = {By developing a wide-field scheme for spectral measurement and implementing photoswitching, we synchronously obtained the fluorescence spectra and positions of ∼10 6 single molecules in labeled cells in minutes, which consequently enabled spectrally resolved, 'true-color' super-resolution microscopy. The method, called spectrally resolved stochastic optical reconstruction microscopy (SR-STORM), achieved cross-talk-free three-dimensional (3D) imaging for four dyes 10 nm apart in emission spectrum. Excellent resolution was obtained for every channel, and 3D localizations of all molecules were automatically aligned within one imaging path.},
added-at = {2020-03-23T21:12:34.000+0100},
author = {Zhang, Zhengyang and Kenny, Samuel J. and Hauser, Margaret and Li, Wan and Xu, Ke},
biburl = {https://www.bibsonomy.org/bibtex/284897dbac0aaf2637b0895ae8f44c1a5/kfriedl},
doi = {10.1038/nmeth.3528},
file = {:C$\backslash$:/Users/Karoline/AppData/Local/Mendeley Ltd/Mendeley Desktop/Downloaded/uhtp{\_}smlm.pdf:pdf},
interhash = {353017942e50d28f9e6e5b01f062be0c},
intrahash = {84897dbac0aaf2637b0895ae8f44c1a5},
issn = {15487105},
journal = {Nature Methods},
keywords = {3D fluorescence high-throughput microscopy spectral_demixing superresolution},
number = 10,
pages = {935--938},
timestamp = {2020-04-07T11:46:43.000+0200},
title = {{Ultrahigh-throughput single-molecule spectroscopy and spectrally resolved super-resolution microscopy}},
volume = 12,
year = 2015
}