4.8 Article

Photoactivation of silicon rhodamines via a light-induced protonation

Journal

NATURE COMMUNICATIONS
Volume 10, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-12480-3

Keywords

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Funding

  1. Max Planck Society
  2. Ecole Polytechnique Federale de Lausanne
  3. Swiss Commission for Technology and Innovation (CTI)
  4. NCCR Chemical Biology
  5. European Molecular Biology Laboratory
  6. EMBL International PhD Program
  7. European Research Council [ERC CoG-724489]
  8. National Institutes of Health Common Fund 4D Nucleome Program [U01 EB021223/U01, DA047728]
  9. Advanced Light Microscopy Facility (ALMF) at the European Molecular Biology Laboratory (EMBL)
  10. Leica Microsystems for support

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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.

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