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Photochemical Activation of Tertiary Amines for Applications in Studying Cell Physiology.

Naeem AsadDavide DeodatoXin LanMagnus B WidegrenDavid Lee PhillipsLili DuTimothy M Dore
Published in: Journal of the American Chemical Society (2017)
Representative tertiary amines were linked to the 8-cyano-7-hydroxyquinolinyl (CyHQ) photoremovable protecting group (PPG) to create photoactivatable forms suitable for use in studying cell physiology. The photoactivation of tamoxifen and 4-hydroxytamoxifen, which can be used to activate Cre recombinase and CRISPR-Cas9 gene editing, demonstrated that highly efficient release of bioactive molecules could be achieved through one- and two-photon excitation (1PE and 2PE). CyHQ-protected anilines underwent a photoaza-Claisen rearrangement instead of releasing amines. Time-resolved spectroscopic studies revealed that photorelease of the tertiary amines was extremely fast, occurring from a singlet excited state of CyHQ on the 70 ps time scale.
Keyphrases
  • highly efficient
  • single cell
  • crispr cas
  • cell therapy
  • genome editing
  • molecular docking
  • breast cancer cells
  • energy transfer
  • living cells
  • case control
  • fluorescent probe