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SRRF: Universal live-cell super-resolution microscopy

Super-resolution microscopy techniques break the diffraction limit of conventional optical microscopy to achieve resolutions approaching tens of nanometres. The major advantage of such techniques is that they provide resolutions close to those obtainable with electron microscopy while maintaining th...

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Detalles Bibliográficos
Autores principales: Culley, Siân, Tosheva, Kalina L., Matos Pereira, Pedro, Henriques, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025290/
https://www.ncbi.nlm.nih.gov/pubmed/29852248
http://dx.doi.org/10.1016/j.biocel.2018.05.014
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author Culley, Siân
Tosheva, Kalina L.
Matos Pereira, Pedro
Henriques, Ricardo
author_facet Culley, Siân
Tosheva, Kalina L.
Matos Pereira, Pedro
Henriques, Ricardo
author_sort Culley, Siân
collection PubMed
description Super-resolution microscopy techniques break the diffraction limit of conventional optical microscopy to achieve resolutions approaching tens of nanometres. The major advantage of such techniques is that they provide resolutions close to those obtainable with electron microscopy while maintaining the benefits of light microscopy such as a wide palette of high specificity molecular labels, straightforward sample preparation and live-cell compatibility. Despite this, the application of super-resolution microscopy to dynamic, living samples has thus far been limited and often requires specialised, complex hardware. Here we demonstrate how a novel analytical approach, Super-Resolution Radial Fluctuations (SRRF), is able to make live-cell super-resolution microscopy accessible to a wider range of researchers. We show its applicability to live samples expressing GFP using commercial confocal as well as laser- and LED-based widefield microscopes, with the latter achieving long-term timelapse imaging with minimal photobleaching.
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spelling pubmed-60252902018-08-01 SRRF: Universal live-cell super-resolution microscopy Culley, Siân Tosheva, Kalina L. Matos Pereira, Pedro Henriques, Ricardo Int J Biochem Cell Biol Article Super-resolution microscopy techniques break the diffraction limit of conventional optical microscopy to achieve resolutions approaching tens of nanometres. The major advantage of such techniques is that they provide resolutions close to those obtainable with electron microscopy while maintaining the benefits of light microscopy such as a wide palette of high specificity molecular labels, straightforward sample preparation and live-cell compatibility. Despite this, the application of super-resolution microscopy to dynamic, living samples has thus far been limited and often requires specialised, complex hardware. Here we demonstrate how a novel analytical approach, Super-Resolution Radial Fluctuations (SRRF), is able to make live-cell super-resolution microscopy accessible to a wider range of researchers. We show its applicability to live samples expressing GFP using commercial confocal as well as laser- and LED-based widefield microscopes, with the latter achieving long-term timelapse imaging with minimal photobleaching. Elsevier 2018-08 /pmc/articles/PMC6025290/ /pubmed/29852248 http://dx.doi.org/10.1016/j.biocel.2018.05.014 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Culley, Siân
Tosheva, Kalina L.
Matos Pereira, Pedro
Henriques, Ricardo
SRRF: Universal live-cell super-resolution microscopy
title SRRF: Universal live-cell super-resolution microscopy
title_full SRRF: Universal live-cell super-resolution microscopy
title_fullStr SRRF: Universal live-cell super-resolution microscopy
title_full_unstemmed SRRF: Universal live-cell super-resolution microscopy
title_short SRRF: Universal live-cell super-resolution microscopy
title_sort srrf: universal live-cell super-resolution microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025290/
https://www.ncbi.nlm.nih.gov/pubmed/29852248
http://dx.doi.org/10.1016/j.biocel.2018.05.014
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