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BODIPYs with Photoactivatable Fluorescence

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 27, Issue 44, Pages 11257-11267

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202101628

Keywords

BODIPY; fluorescence; imaging; photoactivatable fluorophores; photocages

Funding

  1. National Science Foundation [CHE-1954430]

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The borondipyrromethene (BODIPY) chromophore is a versatile platform for constructing photoresponsive dyes with unique properties, allowing for spatiotemporal control of fluorescence and implementation of imaging strategies that are impossible with conventional fluorophores.
The borondipyrromethene (BODIPY) chromophore is a versatile platform for the construction of photoresponsive dyes with unique properties. Specifically, its covalent connection to a photocleavable group can be exploited to engineer compounds with photoswitchable fluorescence. The resulting photoactivatable fluorophores can increase their emission intensity or shift their emission wavelengths in response to switching. Such changes permit the spatiotemporal control of fluorescence with optical stimulations and the implementation of imaging strategies that would be impossible to replicate with conventional fluorophores. Indeed, BODIPYs with photoactivatable fluorescence enable the selective highlighting of intracellular targets, the nanoscaled visualization of sub-cellular components, the real-time monitoring of dynamic events and the photochemical writing of optical barcodes.

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