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

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Authors: Richard Lincoln, Alexey N. Butkevich, Clara‐Marie Gürth, Alena Fischer, Jessica Matthias, Anna R Emmerich, Maximilian Fidlin, Mariano L. Bossi, Stefan W. Hell
Cited by: 2
References: 46

Abstract

State-of-the-art super-resolution microscopy methods benefit 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 labeling, undergoing byproduct-free photoactivation to yield bright and photostable fluorophores that can be readily imaged by STED (stimulated emission depletion), PALM (photoactivated localization microscopy), or MINFLUX (minimal photon fluxes) nanoscopy techniques. The labels derived from these photoactivatable dyes open up new possibilities for multiplexed imaging.

Fields of Study & Subjects

Luminescence and Fluorescent Materials Photochromic and Fluorescence Chemistry Molecular Sensors and Ion Detection

Publication details

Journal / source
Chem
Publisher
Elsevier BV
Volume
12
Issue
5
Pages
102866–102866
Publication date
2 February 2026
Language
EN