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Superresolution microscopy with novel BODIPY-based fluorophores

Multicolor single-molecule localization microscopy (SMLM) expands our understanding of subcellular details and enables the study of biomolecular interactions through precise visualization of multiple molecules in a single sample with resolution of ~10–20 nm. Probe selection is vital to multicolor SM...

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Autores principales: Bittel, Amy M., Saldivar, Isaac S., Dolman, Nick J., Nan, Xiaolin, Gibbs, Summer L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203453/
https://www.ncbi.nlm.nih.gov/pubmed/30366346
http://dx.doi.org/10.1371/journal.pone.0206104
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author Bittel, Amy M.
Saldivar, Isaac S.
Dolman, Nick J.
Nan, Xiaolin
Gibbs, Summer L.
author_facet Bittel, Amy M.
Saldivar, Isaac S.
Dolman, Nick J.
Nan, Xiaolin
Gibbs, Summer L.
author_sort Bittel, Amy M.
collection PubMed
description Multicolor single-molecule localization microscopy (SMLM) expands our understanding of subcellular details and enables the study of biomolecular interactions through precise visualization of multiple molecules in a single sample with resolution of ~10–20 nm. Probe selection is vital to multicolor SMLM, as the fluorophores must not only exhibit minimal spectral crosstalk, but also be compatible with the same photochemical conditions that promote fluorophore photoswitching. While there are numerous commercially available photoswitchable fluorophores that are optimally excited in the standard Cy3 channel, they are restricted to short Stokes shifts (<30 nm), limiting the number of colors that can be resolved in a single sample. Furthermore, while imaging buffers have been thoroughly examined for commonly used fluorophore scaffolds including cyanine, rhodamine, and oxazine, optimal conditions have not been found for the BODIPY scaffold, precluding its routine use for multicolor SMLM. Herein, we screened common imaging buffer conditions including seven redox reagents with five additives, resulting in 35 overall imaging buffer conditions to identify compatible combinations for BODIPY-based fluorophores. We then demonstrated that novel, photoswitchable BODIPY-based fluorophores with varied length Stokes shifts provide additional color options for SMLM using a combination of BODIPY-based and commercially available photoswitchable fluorophores.
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spelling pubmed-62034532018-11-19 Superresolution microscopy with novel BODIPY-based fluorophores Bittel, Amy M. Saldivar, Isaac S. Dolman, Nick J. Nan, Xiaolin Gibbs, Summer L. PLoS One Research Article Multicolor single-molecule localization microscopy (SMLM) expands our understanding of subcellular details and enables the study of biomolecular interactions through precise visualization of multiple molecules in a single sample with resolution of ~10–20 nm. Probe selection is vital to multicolor SMLM, as the fluorophores must not only exhibit minimal spectral crosstalk, but also be compatible with the same photochemical conditions that promote fluorophore photoswitching. While there are numerous commercially available photoswitchable fluorophores that are optimally excited in the standard Cy3 channel, they are restricted to short Stokes shifts (<30 nm), limiting the number of colors that can be resolved in a single sample. Furthermore, while imaging buffers have been thoroughly examined for commonly used fluorophore scaffolds including cyanine, rhodamine, and oxazine, optimal conditions have not been found for the BODIPY scaffold, precluding its routine use for multicolor SMLM. Herein, we screened common imaging buffer conditions including seven redox reagents with five additives, resulting in 35 overall imaging buffer conditions to identify compatible combinations for BODIPY-based fluorophores. We then demonstrated that novel, photoswitchable BODIPY-based fluorophores with varied length Stokes shifts provide additional color options for SMLM using a combination of BODIPY-based and commercially available photoswitchable fluorophores. Public Library of Science 2018-10-26 /pmc/articles/PMC6203453/ /pubmed/30366346 http://dx.doi.org/10.1371/journal.pone.0206104 Text en © 2018 Bittel et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bittel, Amy M.
Saldivar, Isaac S.
Dolman, Nick J.
Nan, Xiaolin
Gibbs, Summer L.
Superresolution microscopy with novel BODIPY-based fluorophores
title Superresolution microscopy with novel BODIPY-based fluorophores
title_full Superresolution microscopy with novel BODIPY-based fluorophores
title_fullStr Superresolution microscopy with novel BODIPY-based fluorophores
title_full_unstemmed Superresolution microscopy with novel BODIPY-based fluorophores
title_short Superresolution microscopy with novel BODIPY-based fluorophores
title_sort superresolution microscopy with novel bodipy-based fluorophores
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203453/
https://www.ncbi.nlm.nih.gov/pubmed/30366346
http://dx.doi.org/10.1371/journal.pone.0206104
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