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Optimized Properties and Synthesis of Photoactivatable Diazoketorhodamines Facilitate and Enhance High-Throughput Single-Molecule Tracking.

Nicholas W PinoAnne R SizemoreLeah ClearyHelen LiuDavid T McSwiggenDan SongHilary P BeckKylie ChengMiki HardyJessica HsiungYangzhong TangRajender AnugulaSanthosh LakshmanRavi K MerneediPradipta Sinha
Published in: The Journal of organic chemistry (2024)
Photoactivatable (PA) rhodamine dyes are widely used in single-molecule tracking (SMT) and a variety of other fluorescence-based imaging modalities. One of the most commonly employed scaffolds uses a diazoketone to lock the rhodamine in the nonfluorescent closed form, which can be activated with 405 nm light. However, poor properties of previously reported dyes require significant washing, which can be resource- and cost-intensive, especially when performing microscopy in a large scale and high-throughput fashion. Here, we report improved diazoketorhodamines that perform exceptionally well in single-molecule tracking microscopy. We also report on the optimization of an improved synthetic method for further iteration and tailoring of diazoketorhodamines to the requirements of a specific user.
Keyphrases
  • single molecule
  • high throughput
  • atomic force microscopy
  • living cells
  • single cell
  • fluorescent probe
  • high resolution
  • photodynamic therapy
  • aqueous solution
  • optical coherence tomography
  • quantum dots