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Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays
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 ph...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278358/ https://www.ncbi.nlm.nih.gov/pubmed/30428589 http://dx.doi.org/10.3390/molecules23112960 |
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author | Ruthenbeck, Alexandra Marangoni, Elisa Diercks, Björn-Ph. Krüger, Aileen Froese, Alexander Bork, Nadja I. Nikolaev, Viacheslav O. Guse, Andreas H. Meier, Chris |
author_facet | Ruthenbeck, Alexandra Marangoni, Elisa Diercks, Björn-Ph. Krüger, Aileen Froese, Alexander Bork, Nadja I. Nikolaev, Viacheslav O. Guse, Andreas H. Meier, Chris |
author_sort | Ruthenbeck, Alexandra |
collection | PubMed |
description | 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 Ca(2+) 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. |
format | Online Article Text |
id | pubmed-6278358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62783582018-12-13 Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays Ruthenbeck, Alexandra Marangoni, Elisa Diercks, Björn-Ph. Krüger, Aileen Froese, Alexander Bork, Nadja I. Nikolaev, Viacheslav O. Guse, Andreas H. Meier, Chris Molecules Article 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 Ca(2+) 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. MDPI 2018-11-13 /pmc/articles/PMC6278358/ /pubmed/30428589 http://dx.doi.org/10.3390/molecules23112960 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ruthenbeck, Alexandra Marangoni, Elisa Diercks, Björn-Ph. Krüger, Aileen Froese, Alexander Bork, Nadja I. Nikolaev, Viacheslav O. Guse, Andreas H. Meier, Chris Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays |
title | Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays |
title_full | Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays |
title_fullStr | Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays |
title_full_unstemmed | Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays |
title_short | Membrane-Permeable Octanoyloxybenzyl-Masked cNMPs As Novel Tools for Non-Invasive Cell Assays |
title_sort | membrane-permeable octanoyloxybenzyl-masked cnmps as novel tools for non-invasive cell assays |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278358/ https://www.ncbi.nlm.nih.gov/pubmed/30428589 http://dx.doi.org/10.3390/molecules23112960 |
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