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An Improved Targeted cAMP Sensor to Study the Regulation of Adenylyl Cyclase 8 by Ca(2+) Entry through Voltage-Gated Channels

Here we describe an improved sensor with reduced pH sensitivity tethered to adenylyl cyclase (AC) 8. The sensor was used to study cAMP dynamics in the AC8 microdomain of MIN6 cells, a pancreatic β-cell line. In these cells, AC8 was activated by Ca(2+) entry through L-type voltage-gated channels foll...

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Detalles Bibliográficos
Autores principales: Everett, Katy L., Cooper, Dermot M. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781085/
https://www.ncbi.nlm.nih.gov/pubmed/24086669
http://dx.doi.org/10.1371/journal.pone.0075942
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author Everett, Katy L.
Cooper, Dermot M. F.
author_facet Everett, Katy L.
Cooper, Dermot M. F.
author_sort Everett, Katy L.
collection PubMed
description Here we describe an improved sensor with reduced pH sensitivity tethered to adenylyl cyclase (AC) 8. The sensor was used to study cAMP dynamics in the AC8 microdomain of MIN6 cells, a pancreatic β-cell line. In these cells, AC8 was activated by Ca(2+) entry through L-type voltage-gated channels following depolarisation. This activation could be reconstituted in HEK293 cells co-expressing AC8 and either the α1C or α1D subunit of L-type voltage-gated Ca(2+) channels. The development of this improved sensor opens the door to the study of cAMP microdomains in excitable cells that have previously been challenging due to the sensitivity of fluorescent proteins to pH changes.
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spelling pubmed-37810852013-10-01 An Improved Targeted cAMP Sensor to Study the Regulation of Adenylyl Cyclase 8 by Ca(2+) Entry through Voltage-Gated Channels Everett, Katy L. Cooper, Dermot M. F. PLoS One Research Article Here we describe an improved sensor with reduced pH sensitivity tethered to adenylyl cyclase (AC) 8. The sensor was used to study cAMP dynamics in the AC8 microdomain of MIN6 cells, a pancreatic β-cell line. In these cells, AC8 was activated by Ca(2+) entry through L-type voltage-gated channels following depolarisation. This activation could be reconstituted in HEK293 cells co-expressing AC8 and either the α1C or α1D subunit of L-type voltage-gated Ca(2+) channels. The development of this improved sensor opens the door to the study of cAMP microdomains in excitable cells that have previously been challenging due to the sensitivity of fluorescent proteins to pH changes. Public Library of Science 2013-09-23 /pmc/articles/PMC3781085/ /pubmed/24086669 http://dx.doi.org/10.1371/journal.pone.0075942 Text en © 2013 Everett et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Everett, Katy L.
Cooper, Dermot M. F.
An Improved Targeted cAMP Sensor to Study the Regulation of Adenylyl Cyclase 8 by Ca(2+) Entry through Voltage-Gated Channels
title An Improved Targeted cAMP Sensor to Study the Regulation of Adenylyl Cyclase 8 by Ca(2+) Entry through Voltage-Gated Channels
title_full An Improved Targeted cAMP Sensor to Study the Regulation of Adenylyl Cyclase 8 by Ca(2+) Entry through Voltage-Gated Channels
title_fullStr An Improved Targeted cAMP Sensor to Study the Regulation of Adenylyl Cyclase 8 by Ca(2+) Entry through Voltage-Gated Channels
title_full_unstemmed An Improved Targeted cAMP Sensor to Study the Regulation of Adenylyl Cyclase 8 by Ca(2+) Entry through Voltage-Gated Channels
title_short An Improved Targeted cAMP Sensor to Study the Regulation of Adenylyl Cyclase 8 by Ca(2+) Entry through Voltage-Gated Channels
title_sort improved targeted camp sensor to study the regulation of adenylyl cyclase 8 by ca(2+) entry through voltage-gated channels
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781085/
https://www.ncbi.nlm.nih.gov/pubmed/24086669
http://dx.doi.org/10.1371/journal.pone.0075942
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