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A general method to fine-tune fluorophores for live-cell and in vivo imaging

Pushing the frontier of fluorescence microscopy requires the design of enhanced fluorophores with finely tuned properties. We recently discovered that incorporation of four-membered azetidine rings into classic fluorophore structures elicits substantial increases in brightness and photostability, re...

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Autores principales: Grimm, Jonathan B., Muthusamy, Anand K., Liang, Yajie, Brown, Timothy A., Lemon, William C., Patel, Ronak, Lu, Rongwen, Macklin, John J., Keller, Phillip J., Ji, Na, Lavis, Luke D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621985/
https://www.ncbi.nlm.nih.gov/pubmed/28869757
http://dx.doi.org/10.1038/nmeth.4403
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author Grimm, Jonathan B.
Muthusamy, Anand K.
Liang, Yajie
Brown, Timothy A.
Lemon, William C.
Patel, Ronak
Lu, Rongwen
Macklin, John J.
Keller, Phillip J.
Ji, Na
Lavis, Luke D.
author_facet Grimm, Jonathan B.
Muthusamy, Anand K.
Liang, Yajie
Brown, Timothy A.
Lemon, William C.
Patel, Ronak
Lu, Rongwen
Macklin, John J.
Keller, Phillip J.
Ji, Na
Lavis, Luke D.
author_sort Grimm, Jonathan B.
collection PubMed
description Pushing the frontier of fluorescence microscopy requires the design of enhanced fluorophores with finely tuned properties. We recently discovered that incorporation of four-membered azetidine rings into classic fluorophore structures elicits substantial increases in brightness and photostability, resulting in the ‘Janelia Fluor’ (JF) series of dyes. Here, we refine and extend this strategy, showing that incorporation of 3-substituted azetidine groups allows rational tuning of the spectral and chemical properties with unprecedented precision. This strategy yields a palette of new fluorescent and fluorogenic labels with excitation ranging from blue to the far-red with utility in cells, tissue, and animals.
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spelling pubmed-56219852018-03-04 A general method to fine-tune fluorophores for live-cell and in vivo imaging Grimm, Jonathan B. Muthusamy, Anand K. Liang, Yajie Brown, Timothy A. Lemon, William C. Patel, Ronak Lu, Rongwen Macklin, John J. Keller, Phillip J. Ji, Na Lavis, Luke D. Nat Methods Article Pushing the frontier of fluorescence microscopy requires the design of enhanced fluorophores with finely tuned properties. We recently discovered that incorporation of four-membered azetidine rings into classic fluorophore structures elicits substantial increases in brightness and photostability, resulting in the ‘Janelia Fluor’ (JF) series of dyes. Here, we refine and extend this strategy, showing that incorporation of 3-substituted azetidine groups allows rational tuning of the spectral and chemical properties with unprecedented precision. This strategy yields a palette of new fluorescent and fluorogenic labels with excitation ranging from blue to the far-red with utility in cells, tissue, and animals. 2017-09-04 2017-10 /pmc/articles/PMC5621985/ /pubmed/28869757 http://dx.doi.org/10.1038/nmeth.4403 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Grimm, Jonathan B.
Muthusamy, Anand K.
Liang, Yajie
Brown, Timothy A.
Lemon, William C.
Patel, Ronak
Lu, Rongwen
Macklin, John J.
Keller, Phillip J.
Ji, Na
Lavis, Luke D.
A general method to fine-tune fluorophores for live-cell and in vivo imaging
title A general method to fine-tune fluorophores for live-cell and in vivo imaging
title_full A general method to fine-tune fluorophores for live-cell and in vivo imaging
title_fullStr A general method to fine-tune fluorophores for live-cell and in vivo imaging
title_full_unstemmed A general method to fine-tune fluorophores for live-cell and in vivo imaging
title_short A general method to fine-tune fluorophores for live-cell and in vivo imaging
title_sort general method to fine-tune fluorophores for live-cell and in vivo imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621985/
https://www.ncbi.nlm.nih.gov/pubmed/28869757
http://dx.doi.org/10.1038/nmeth.4403
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