Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging

The ability to quantify the organization of cell membrane molecules is limited by the density of labeling and experimental conditions. Here, the authors use super-resolution optical fluctuation (SOFI) for molecular density and clustering analyses, and investigate nanoscale distribution of CD4 glycop...

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Autores principales:	Tomáš Lukeš, Daniela Glatzová, Zuzana Kvíčalová, Florian Levet, Aleš Benda, Sebastian Letschert, Markus Sauer, Tomáš Brdička, Theo Lasser, Marek Cebecauer
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2017
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/3c01c52f65f749888df9da458d18ffa1
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spelling	oai:doaj.org-article:3c01c52f65f749888df9da458d18ffa12021-12-02T15:38:54ZQuantifying protein densities on cell membranes using super-resolution optical fluctuation imaging10.1038/s41467-017-01857-x2041-1723https://doaj.org/article/3c01c52f65f749888df9da458d18ffa12017-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-01857-xhttps://doaj.org/toc/2041-1723The ability to quantify the organization of cell membrane molecules is limited by the density of labeling and experimental conditions. Here, the authors use super-resolution optical fluctuation (SOFI) for molecular density and clustering analyses, and investigate nanoscale distribution of CD4 glycoprotein.Tomáš LukešDaniela GlatzováZuzana KvíčalováFlorian LevetAleš BendaSebastian LetschertMarkus SauerTomáš BrdičkaTheo LasserMarek CebecauerNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-7 (2017)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Tomáš Lukeš Daniela Glatzová Zuzana Kvíčalová Florian Levet Aleš Benda Sebastian Letschert Markus Sauer Tomáš Brdička Theo Lasser Marek Cebecauer Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging
description	The ability to quantify the organization of cell membrane molecules is limited by the density of labeling and experimental conditions. Here, the authors use super-resolution optical fluctuation (SOFI) for molecular density and clustering analyses, and investigate nanoscale distribution of CD4 glycoprotein.
format	article
author	Tomáš Lukeš Daniela Glatzová Zuzana Kvíčalová Florian Levet Aleš Benda Sebastian Letschert Markus Sauer Tomáš Brdička Theo Lasser Marek Cebecauer
author_facet	Tomáš Lukeš Daniela Glatzová Zuzana Kvíčalová Florian Levet Aleš Benda Sebastian Letschert Markus Sauer Tomáš Brdička Theo Lasser Marek Cebecauer
author_sort	Tomáš Lukeš
title	Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging
title_short	Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging
title_full	Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging
title_fullStr	Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging
title_full_unstemmed	Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging
title_sort	quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging
publisher	Nature Portfolio
publishDate	2017
url	https://doaj.org/article/3c01c52f65f749888df9da458d18ffa1
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Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging

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