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Photoactivation of silicon rhodamines via a light-induced protonation

Photoactivatable fluorophores are important for single-particle tracking and super-resolution microscopy. Here we present a photoactivatable fluorophore that forms a bright silicon rhodamine derivative through a light-dependent protonation. In contrast to other photoactivatable fluorophores, no cagi...

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Detalles Bibliográficos
Autores principales: Frei, Michelle S., Hoess, Philipp, Lampe, Marko, Nijmeijer, Bianca, Kueblbeck, Moritz, Ellenberg, Jan, Wadepohl, Hubert, Ries, Jonas, Pitsch, Stefan, Reymond, Luc, Johnsson, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783549/
https://www.ncbi.nlm.nih.gov/pubmed/31594948
http://dx.doi.org/10.1038/s41467-019-12480-3
Descripción
Sumario:Photoactivatable fluorophores are important for single-particle tracking and super-resolution microscopy. Here we present a photoactivatable fluorophore that forms a bright silicon rhodamine derivative through a light-dependent protonation. In contrast to other photoactivatable fluorophores, no caging groups are required, nor are there any undesired side-products released. Using this photoactivatable fluorophore, we create probes for HaloTag and actin for live-cell single-molecule localization microscopy and single-particle tracking experiments. The unusual mechanism of photoactivation and the fluorophore’s outstanding spectroscopic properties make it a powerful tool for live-cell super-resolution microscopy.