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Epac-Inhibitors: Facts and Artefacts

cAMP is a universal second messenger. Its signalling is mediated by protein kinase A, Epac and certain types of ion channels in mammalians. cAMP signalling is involved in many physiological processes ranging from vision to the control of insulin secretion, pacemaker activity and gene transcription a...

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Detalles Bibliográficos
Autor principal: Rehmann, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805970/
https://www.ncbi.nlm.nih.gov/pubmed/24149987
http://dx.doi.org/10.1038/srep03032
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author Rehmann, Holger
author_facet Rehmann, Holger
author_sort Rehmann, Holger
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description cAMP is a universal second messenger. Its signalling is mediated by protein kinase A, Epac and certain types of ion channels in mammalians. cAMP signalling is involved in many physiological processes ranging from vision to the control of insulin secretion, pacemaker activity and gene transcription and therefore selective pharmacological interference is of medical interest. Whereas selective inhibitors of PKA and selective activators of Epac are well established, no inhibitors of Epac were available until recently. Here the action of four of the novel Epac inhibitors was analysed by biophysical means. ESI-05 is confirmed as a selective inhibitor of Epac2. No direct action of Brefeldin A on Epac could be demonstrated. ESI-09 and HJC0197 were found to act as chemicals with general protein denaturing properties and do not act on Epac selectively.
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spelling pubmed-38059702013-10-23 Epac-Inhibitors: Facts and Artefacts Rehmann, Holger Sci Rep Article cAMP is a universal second messenger. Its signalling is mediated by protein kinase A, Epac and certain types of ion channels in mammalians. cAMP signalling is involved in many physiological processes ranging from vision to the control of insulin secretion, pacemaker activity and gene transcription and therefore selective pharmacological interference is of medical interest. Whereas selective inhibitors of PKA and selective activators of Epac are well established, no inhibitors of Epac were available until recently. Here the action of four of the novel Epac inhibitors was analysed by biophysical means. ESI-05 is confirmed as a selective inhibitor of Epac2. No direct action of Brefeldin A on Epac could be demonstrated. ESI-09 and HJC0197 were found to act as chemicals with general protein denaturing properties and do not act on Epac selectively. Nature Publishing Group 2013-10-23 /pmc/articles/PMC3805970/ /pubmed/24149987 http://dx.doi.org/10.1038/srep03032 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Rehmann, Holger
Epac-Inhibitors: Facts and Artefacts
title Epac-Inhibitors: Facts and Artefacts
title_full Epac-Inhibitors: Facts and Artefacts
title_fullStr Epac-Inhibitors: Facts and Artefacts
title_full_unstemmed Epac-Inhibitors: Facts and Artefacts
title_short Epac-Inhibitors: Facts and Artefacts
title_sort epac-inhibitors: facts and artefacts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805970/
https://www.ncbi.nlm.nih.gov/pubmed/24149987
http://dx.doi.org/10.1038/srep03032
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