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Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays.

Alexandra RuthenbeckElisa MarangoniBjörn-Philipp DiercksAileen KrügerAlexander FroeseNadja I BorkViacheslav O NikolaevAndreas H GuseChris Meier
Published in: Molecules (Basel, Switzerland) (2018)
Adenine nucleotide (AN) 2nd messengers, such as 3',5'-cyclic adenosine monophosphate (cAMP), are central elements of intracellular signaling, but many details of their underlying processes remain elusive. Like all nucleotides, cyclic nucleotide monophosphates (cNMPs) are net-negatively charged at physiologic pH which limits their applicability in cell-based settings. Thus, many cellular assays rely on sophisticated techniques like microinjection or electroporation. This setup is not feasible for medium- to high-throughput formats, and the mechanic stress that cells are exposed to raises the probability of interfering artefacts or false-positives. Here, we present a short and flexible chemical route yielding membrane-permeable, bio-reversibly masked cNMPs for which we employed the octanoyloxybenzyl (OB) group. We further show hydrolysis studies on chemical stability and enzymatic activation, and present results of real-time assays, where we used cAMP and Ca2+ live cell imaging to demonstrate high permeability and prompt intracellular conversion of some selected masked cNMPs. Based on these results, our novel OB-masked cNMPs constitute valuable precursor-tools for non-invasive studies on intracellular signaling.
Keyphrases
  • high throughput
  • single cell
  • reactive oxygen species
  • induced apoptosis
  • high resolution
  • binding protein
  • hydrogen peroxide
  • cell cycle arrest
  • endothelial cells
  • nitric oxide
  • oxidative stress
  • mesenchymal stem cells