Abstract
We have reengineered a red-emitting dicyanomethylenedihydrofuran push-pull fluorophore so that it is dark until photoactivated with a short burst of low-intensity violet light. Photoactivation of the dark fluorogen leads to conversion of an azide to an amine, which shifts the absorption to long wavelengths. After photoactivation, the fluorophore is bright and photostable enough to be imaged on the single-molecule level in living cells. This proof-of-principle demonstration provides a new class of bright photoactivatable fluorophores, as are needed for super-resolution imaging schemes that require active control of single molecule emission.
MeSH Terms
Animals
Azides/chemical synthesis,chemistry
CHO Cells
Cricetinae
Cricetulus
Fluorescent Dyes/chemical synthesis,chemistry
Furans/chemical synthesis,chemistry
Nitriles/chemical synthesis,chemistry
Photochemistry
Spectrometry, Fluorescence/methods
Chemicals
Azides
Fluorescent Dyes
Furans
Nitriles
dicyanomethylenedihydrofuran
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Lord Samuel J
Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.
Conley Nicholas R
Lee Hsiao-lu D
Samuel Reichel
Liu Na
Twieg Robert J
Moerner W E
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