Photoactivatable, biologically-relevant phenols with sensitivity toward 2-photon excitation. Issue 12 (15th October 2015)

• Record Type: Journal Article
• Authors: McLain, Duncan E.; Rea, Adam. C.; Widegren, Magnus B.; Dore, Timothy M.
• Is Part Of: Photochemical & photobiological sciences. Volume 14:Issue 12(2015:Dec.)
• Page Start: 2151
• Page End: 2158
• Publication Date: 2015-10-15
• Subjects: Photochemistry -- Periodicals; Photobiology -- Periodicals; 541.35
• DOI: 10.1039/c5pp00334b
• Languages: English
• ISSNs: 1474-905X

Abstract

Abstract : Quinoline-based photoremovable protecting groups mediate the photoactivation of the signaling molecules serotonin, octopamine, capsaicin, N -vanillyl-nonanoylamide, estradiol, and tyrosine through 1- and 2-photon excitation and enable physiological studies. Abstract : Spatio-temporal release of biologically relevant small molecules provides exquisite control over the activation of receptors and signaling pathways. This can be accomplished via a photochemical reaction that releases the desired small molecule in response to irradiation with light. A series of biologically-relevant signaling molecules (serotonin, octopamine, capsaicin, N -vanillyl-nonanoylamide, estradiol, and tyrosine) that contain a phenol moiety were conjugated to the 8-bromo-7-hydroxyquinolinyl (BHQ) or 8-cyano-7-hydroxyquinolinyl (CyHQ) photoremovable protecting groups (PPGs). The CyHQ caged compounds proved sensitive toward 1PE and 2PE processes with quantum efficiencies of 0.2–0.4 upon irradiation at 365 nm and two-photon action cross sections of 0.15–0.31 GM when irradiated at 740 nm. All but one BHQ caged compound, BHQ-estradiol, were found to be sensitive to photolysis through 1PE and 2PE with quantum efficiencies of 0.30–0.40 and two photon cross sections of 0.40–0.60 GM. Instead of releasing estradiol, BHQ-estradiol underwent debromination.