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Electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system
Ion channels are located in plasma membranes as well as on mitochondrial, lysosomal, and endoplasmic reticulum membranes. They play a critical role in physiology and drug targeting. It is particularly challenging to measure the current mediated by ion channels in the lysosomal and the endoplasmic re...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269590/ https://www.ncbi.nlm.nih.gov/pubmed/30504856 http://dx.doi.org/10.1038/s41598-018-35316-4 |
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author | Kamiya, Koki Osaki, Toshihisa Nakao, Kenji Kawano, Ryuji Fujii, Satoshi Misawa, Nobuo Hayakawa, Masatoshi Takeuchi, Shoji |
author_facet | Kamiya, Koki Osaki, Toshihisa Nakao, Kenji Kawano, Ryuji Fujii, Satoshi Misawa, Nobuo Hayakawa, Masatoshi Takeuchi, Shoji |
author_sort | Kamiya, Koki |
collection | PubMed |
description | Ion channels are located in plasma membranes as well as on mitochondrial, lysosomal, and endoplasmic reticulum membranes. They play a critical role in physiology and drug targeting. It is particularly challenging to measure the current mediated by ion channels in the lysosomal and the endoplasmic reticulum membranes using the conventional patch clamp method. In this study, we show that our proposed device is applicable for an electrophysiological measurement of various types of ion channel in plasma and organelle membranes. We designed an on-chip device that can form multiple electrical contacts with a measurement system when placed on a mount system. Using crude cell membranes containing ion channels extracted from cultured cells without detergents, we detected open/close signals of the hERG, TRPV1, and NMDA channels on plasma membranes, those of the TRPML1 channels on lysosomal membranes, and open/close signals of the RyR channels on SR membranes. This method will provide a highly versatile drug screening system for ion channels expressed by various cell membranes, including plasma, SR, mitochondrial, Golgi, and lysosomal membranes. |
format | Online Article Text |
id | pubmed-6269590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62695902018-12-05 Electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system Kamiya, Koki Osaki, Toshihisa Nakao, Kenji Kawano, Ryuji Fujii, Satoshi Misawa, Nobuo Hayakawa, Masatoshi Takeuchi, Shoji Sci Rep Article Ion channels are located in plasma membranes as well as on mitochondrial, lysosomal, and endoplasmic reticulum membranes. They play a critical role in physiology and drug targeting. It is particularly challenging to measure the current mediated by ion channels in the lysosomal and the endoplasmic reticulum membranes using the conventional patch clamp method. In this study, we show that our proposed device is applicable for an electrophysiological measurement of various types of ion channel in plasma and organelle membranes. We designed an on-chip device that can form multiple electrical contacts with a measurement system when placed on a mount system. Using crude cell membranes containing ion channels extracted from cultured cells without detergents, we detected open/close signals of the hERG, TRPV1, and NMDA channels on plasma membranes, those of the TRPML1 channels on lysosomal membranes, and open/close signals of the RyR channels on SR membranes. This method will provide a highly versatile drug screening system for ion channels expressed by various cell membranes, including plasma, SR, mitochondrial, Golgi, and lysosomal membranes. Nature Publishing Group UK 2018-11-30 /pmc/articles/PMC6269590/ /pubmed/30504856 http://dx.doi.org/10.1038/s41598-018-35316-4 Text en © The Author(s) 2018 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 Kamiya, Koki Osaki, Toshihisa Nakao, Kenji Kawano, Ryuji Fujii, Satoshi Misawa, Nobuo Hayakawa, Masatoshi Takeuchi, Shoji Electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system |
title | Electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system |
title_full | Electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system |
title_fullStr | Electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system |
title_full_unstemmed | Electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system |
title_short | Electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system |
title_sort | electrophysiological measurement of ion channels on plasma/organelle membranes using an on-chip lipid bilayer system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269590/ https://www.ncbi.nlm.nih.gov/pubmed/30504856 http://dx.doi.org/10.1038/s41598-018-35316-4 |
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