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Organelle membrane derived patches: reshaping classical methods for new targets

Intracellular ion channels are involved in multiple signaling processes, including such crucial ones as regulation of cellular motility and fate. With 95% of the cellular membrane belonging to intracellular organelles, it is hard to overestimate the importance of intracellular ion channels. Multiple...

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Autores principales: Shapovalov, George, Ritaine, Abigaël, Bidaux, Gabriel, Slomianny, Christian, Borowiec, Anne-Sophie, Gordienko, Dmitri, Bultynck, Geert, Skryma, Roman, Prevarskaya, Natalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658434/
https://www.ncbi.nlm.nih.gov/pubmed/29074990
http://dx.doi.org/10.1038/s41598-017-13968-y
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author Shapovalov, George
Ritaine, Abigaël
Bidaux, Gabriel
Slomianny, Christian
Borowiec, Anne-Sophie
Gordienko, Dmitri
Bultynck, Geert
Skryma, Roman
Prevarskaya, Natalia
author_facet Shapovalov, George
Ritaine, Abigaël
Bidaux, Gabriel
Slomianny, Christian
Borowiec, Anne-Sophie
Gordienko, Dmitri
Bultynck, Geert
Skryma, Roman
Prevarskaya, Natalia
author_sort Shapovalov, George
collection PubMed
description Intracellular ion channels are involved in multiple signaling processes, including such crucial ones as regulation of cellular motility and fate. With 95% of the cellular membrane belonging to intracellular organelles, it is hard to overestimate the importance of intracellular ion channels. Multiple studies have been performed on these channels over the years, however, a unified approach allowing not only to characterize their activity but also to study their regulation by partner proteins, analogous to the patch clamp “golden standard”, is lacking. Here, we present a universal approach that combines the extraction of intracellular membrane fractions with the preparation of patchable substrates that allows to characterize these channels in endogenous protein environment and to study their regulation by partner proteins. We validate this method by characterizing activity of multiple intracellular ion channels localized to different organelles and by providing detailed electrophysiological characterization of the regulation of IP(3)R activity by endogenous Bcl-2. Thus, after synthesis and reshaping of the well-established approaches, organelle membrane derived patch clamp provides the means to assess ion channels from arbitrary cellular membranes at the single channel level.
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spelling pubmed-56584342017-10-31 Organelle membrane derived patches: reshaping classical methods for new targets Shapovalov, George Ritaine, Abigaël Bidaux, Gabriel Slomianny, Christian Borowiec, Anne-Sophie Gordienko, Dmitri Bultynck, Geert Skryma, Roman Prevarskaya, Natalia Sci Rep Article Intracellular ion channels are involved in multiple signaling processes, including such crucial ones as regulation of cellular motility and fate. With 95% of the cellular membrane belonging to intracellular organelles, it is hard to overestimate the importance of intracellular ion channels. Multiple studies have been performed on these channels over the years, however, a unified approach allowing not only to characterize their activity but also to study their regulation by partner proteins, analogous to the patch clamp “golden standard”, is lacking. Here, we present a universal approach that combines the extraction of intracellular membrane fractions with the preparation of patchable substrates that allows to characterize these channels in endogenous protein environment and to study their regulation by partner proteins. We validate this method by characterizing activity of multiple intracellular ion channels localized to different organelles and by providing detailed electrophysiological characterization of the regulation of IP(3)R activity by endogenous Bcl-2. Thus, after synthesis and reshaping of the well-established approaches, organelle membrane derived patch clamp provides the means to assess ion channels from arbitrary cellular membranes at the single channel level. Nature Publishing Group UK 2017-10-26 /pmc/articles/PMC5658434/ /pubmed/29074990 http://dx.doi.org/10.1038/s41598-017-13968-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shapovalov, George
Ritaine, Abigaël
Bidaux, Gabriel
Slomianny, Christian
Borowiec, Anne-Sophie
Gordienko, Dmitri
Bultynck, Geert
Skryma, Roman
Prevarskaya, Natalia
Organelle membrane derived patches: reshaping classical methods for new targets
title Organelle membrane derived patches: reshaping classical methods for new targets
title_full Organelle membrane derived patches: reshaping classical methods for new targets
title_fullStr Organelle membrane derived patches: reshaping classical methods for new targets
title_full_unstemmed Organelle membrane derived patches: reshaping classical methods for new targets
title_short Organelle membrane derived patches: reshaping classical methods for new targets
title_sort organelle membrane derived patches: reshaping classical methods for new targets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658434/
https://www.ncbi.nlm.nih.gov/pubmed/29074990
http://dx.doi.org/10.1038/s41598-017-13968-y
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