Coumarin-based octopamine phototriggers and their effects on an insect octopamine receptor

Chembiochem. 2012 Jul 9;13(10):1458-64. doi: 10.1002/cbic.201200110. Epub 2012 Jun 6.

Abstract

We have developed and characterized efficient caged compounds of the neurotransmitter octopamine. For derivatization, we introduced [6-bromo-8-(diethylaminomethyl)-7-hydroxycoumarin-4-yl]methoxycarbonyl (DBHCMOC) and {6-bromo-7-hydroxy-8-[(piperazin-1-yl)methyl]coumarin-4-yl}methoxycarbonyl (PBHCMOC) moieties as novel photo-removable protecting groups. The caged compounds were functionally inactive when applied to heterologously expressed octopamine receptors (AmOctα1R). Upon irradiation with UV-visible or IR light, bioactive octopamine was released and evoked Ca2+ signals in AmOctα1R-expressing cells. The pronounced water solubility of compounds 2-4 in particular holds great promise for these substances as excellent phototriggers of this important neurotransmitter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bees / metabolism
  • Calcium Signaling
  • Carbon Dioxide / chemistry
  • Coumarins / chemistry*
  • HEK293 Cells
  • Humans
  • Infrared Rays
  • Octopamine / chemical synthesis
  • Octopamine / chemistry*
  • Photolysis
  • Receptors, Biogenic Amine / genetics
  • Receptors, Biogenic Amine / metabolism*
  • Solubility
  • Ultraviolet Rays

Substances

  • Coumarins
  • Receptors, Biogenic Amine
  • norsynephrine receptor
  • Carbon Dioxide
  • Octopamine
  • coumarin