| Literature DB >> 24449030 |
Flavie Lavoie-Cardinal1, Nickels A Jensen, Volker Westphal, Andre C Stiel, Andriy Chmyrov, Jakob Bierwagen, Ilaria Testa, Stefan Jakobs, Stefan W Hell.
Abstract
Up to now, all demonstrations of reversible saturable optical fluorescence transitions (RESOLFT) superresolution microscopy of living cells have relied on the use of reversibly switchable fluorescent proteins (RSFP) emitting in the green spectral range. Here we show RESOLFT imaging with rsCherryRev1.4, a new red-emitting RSFP enabling a spatial resolution up to four times higher than the diffraction barrier. By co-expressing green and red RSFPs in living cells we demonstrate two-color RESOLFT imaging both for single ("donut") beam scanning and for parallelized versions of RESOLFT nanoscopy where an array of >23,000 "donut-like" minima are scanned simultaneously. ©2014 The Authors. Published by Wiley-VCH Verlag GmbH&Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.Keywords: RESOLFT; fluorescent proteins; nanoscopy; photoswitching; superresolution imaging
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Year: 2014 PMID: 24449030 DOI: 10.1002/cphc.201301016
Source DB: PubMed Journal: Chemphyschem ISSN: 1439-4235 Impact factor: 3.102