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ChemBiochemistryPeer-reviewed journal article

Caging-group-free photoactivatable fluorophores with far-red emission

Richard LincolniD, Alexey N. ButkevichiD, Clara‐Marie GürthiD, Alena Fischer, Jessica MatthiasiD, Anna R Emmerich, Maximilian Fidlin, Mariano L. BossiiD, Stefan W. HelliD

PDFDOIPreprint
Citations
2
FWCI
5.52
Field percentile
top 7%

Abstract

State of the art super-resolution microscopy methods profit greatly when combined with photoactivatable or photoswitchable fluorophores with far-red emission, but the majority of these fluorophores require specialized buffers or rely on photolabile protecting groups that limit their biocompatibility. We report here a caging-group-free strategy for photoactivatable dyes based on 1-vinyl-10-silaxanthone derivatives containing 9-acylimino or 9-(alkoxycarbonyl)imino groups, enabling minimally-sized photoactivatable dyes with >680 nm emission. The 9-(alkoxycarbonyl)imino silaxanthones are particularly suitable for live-cell labelling, undergoing byproduct-free photoactivation to yield bright and photostable fluorophores that can be readily imaged by STED, PALM, or MINFLUX nanoscopy techniques. The labels derived from these photoactivatable dyes open up new possibilities for multiplexed imaging.

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