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Synthesis of Water-Soluble Far-Red-Emitting Amphiphilic BODIPY Dyes

[Image: see text] We report the synthesis of two water-soluble BODIPY dyes with far-red absorption and near-infrared fluorescence following cell membrane insertion. Introduction of dicationic or dianionic groups imparts water solubility and prevents translocation of the dye through the plasma membra...

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Autores principales: Bardon, Kevin M., Selfridge, Scott, Adams, Dany S., Minns, Richard A., Pawle, Robert, Adams, Timothy C., Takiff, Larry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217593/
https://www.ncbi.nlm.nih.gov/pubmed/30411029
http://dx.doi.org/10.1021/acsomega.8b01487
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author Bardon, Kevin M.
Selfridge, Scott
Adams, Dany S.
Minns, Richard A.
Pawle, Robert
Adams, Timothy C.
Takiff, Larry
author_facet Bardon, Kevin M.
Selfridge, Scott
Adams, Dany S.
Minns, Richard A.
Pawle, Robert
Adams, Timothy C.
Takiff, Larry
author_sort Bardon, Kevin M.
collection PubMed
description [Image: see text] We report the synthesis of two water-soluble BODIPY dyes with far-red absorption and near-infrared fluorescence following cell membrane insertion. Introduction of dicationic or dianionic groups imparts water solubility and prevents translocation of the dye through the plasma membrane for highly effective labeling. The dicationic form is particularly well localized to the plasma membrane and resists quenching even after >8 min of continuous light exposure. The dyes are almost completely nonemissive in water and other highly polar solvents, but display high-fluorescence yields in chloroform and upon insertion into the extracellular leaflet.
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spelling pubmed-62175932018-11-06 Synthesis of Water-Soluble Far-Red-Emitting Amphiphilic BODIPY Dyes Bardon, Kevin M. Selfridge, Scott Adams, Dany S. Minns, Richard A. Pawle, Robert Adams, Timothy C. Takiff, Larry ACS Omega [Image: see text] We report the synthesis of two water-soluble BODIPY dyes with far-red absorption and near-infrared fluorescence following cell membrane insertion. Introduction of dicationic or dianionic groups imparts water solubility and prevents translocation of the dye through the plasma membrane for highly effective labeling. The dicationic form is particularly well localized to the plasma membrane and resists quenching even after >8 min of continuous light exposure. The dyes are almost completely nonemissive in water and other highly polar solvents, but display high-fluorescence yields in chloroform and upon insertion into the extracellular leaflet. American Chemical Society 2018-10-15 /pmc/articles/PMC6217593/ /pubmed/30411029 http://dx.doi.org/10.1021/acsomega.8b01487 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Bardon, Kevin M.
Selfridge, Scott
Adams, Dany S.
Minns, Richard A.
Pawle, Robert
Adams, Timothy C.
Takiff, Larry
Synthesis of Water-Soluble Far-Red-Emitting Amphiphilic BODIPY Dyes
title Synthesis of Water-Soluble Far-Red-Emitting Amphiphilic BODIPY Dyes
title_full Synthesis of Water-Soluble Far-Red-Emitting Amphiphilic BODIPY Dyes
title_fullStr Synthesis of Water-Soluble Far-Red-Emitting Amphiphilic BODIPY Dyes
title_full_unstemmed Synthesis of Water-Soluble Far-Red-Emitting Amphiphilic BODIPY Dyes
title_short Synthesis of Water-Soluble Far-Red-Emitting Amphiphilic BODIPY Dyes
title_sort synthesis of water-soluble far-red-emitting amphiphilic bodipy dyes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217593/
https://www.ncbi.nlm.nih.gov/pubmed/30411029
http://dx.doi.org/10.1021/acsomega.8b01487
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