Source:http://linkedlifedata.com/resource/pubmed/id/20959110
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2010-10-20
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pubmed:abstractText |
Current far-field fluorescence nanoscopes provide subdiffraction resolution by exploiting a mechanism of fluorescence inhibition. This mechanism is implemented such that features closer than the diffraction limit emit separately when simultaneously exposed to excitation light. A basic mechanism for such transient fluorescence inhibition is the depletion of the fluorophore ground state by transferring it (via a triplet) in a dark state, a mechanism which is workable in most standard dyes. Here we show that microscopy based on ground state depletion followed by individual molecule return (GSDIM) can effectively provide multicolor diffraction-unlimited resolution imaging of immunolabeled fixed and SNAP-tag labeled living cells. Implemented with standard labeling techniques, GSDIM is demonstrated to separate up to four different conventional fluorophores using just two detection channels and a single laser line. The method can be expanded to even more colors by choosing optimized dichroic mirrors and selecting marker molecules with negligible inhomogeneous emission broadening.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1542-0086
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pubmed:author |
pubmed-author:EggelingChristianC,
pubmed-author:FöllingJonasJ,
pubmed-author:HellStefan WSW,
pubmed-author:JakobsStefanS,
pubmed-author:MeddaRebeccaR,
pubmed-author:RothermelEllenE,
pubmed-author:SchönleAndreasA,
pubmed-author:TestaIlariaI,
pubmed-author:WurmChristian ACA,
pubmed-author:von MiddendorfClaasC
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pubmed:copyrightInfo |
Copyright © 2010 Biophysical Society. Published by Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
20
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pubmed:volume |
99
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2686-94
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pubmed:dateRevised |
2011-10-20
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pubmed:meshHeading |
pubmed-meshheading:20959110-Animals,
pubmed-meshheading:20959110-Cell Line,
pubmed-meshheading:20959110-Cell Survival,
pubmed-meshheading:20959110-Color,
pubmed-meshheading:20959110-Fluorescent Dyes,
pubmed-meshheading:20959110-Microscopy, Atomic Force,
pubmed-meshheading:20959110-Microscopy, Fluorescence,
pubmed-meshheading:20959110-Nanotechnology,
pubmed-meshheading:20959110-Potoroidae,
pubmed-meshheading:20959110-Spectrometry, Fluorescence
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pubmed:year |
2010
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pubmed:articleTitle |
Multicolor fluorescence nanoscopy in fixed and living cells by exciting conventional fluorophores with a single wavelength.
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pubmed:affiliation |
Department of Nanobiophotonics, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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