Development of an automated system to measure ion channel currents using a surface-modified gold probe

Abstract Artificial lipid bilayer single-channel recording technique has been employed to determine the biophysical and pharmacological properties of various ion channels. However, its measurement efficiency is very low, as it requires two time-consuming processes: preparation of lipid bilayer membr...

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Main Authors: Minako Hirano, Masahisa Tomita, Chikako Takahashi, Nobuyuki Kawashima, Toru Ide
Format: Article
Language:English
Published: Nature Publishing Group 2021-09-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-97237-z
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spelling doaj-7112184ceb324bce85d10222d37eb7e52021-09-12T11:22:53ZengNature Publishing GroupScientific Reports2045-23222021-09-011111910.1038/s41598-021-97237-zDevelopment of an automated system to measure ion channel currents using a surface-modified gold probeMinako Hirano0Masahisa Tomita1Chikako Takahashi2Nobuyuki Kawashima3Toru Ide4The Graduate School for the Creation of New Photonics IndustriesSYSTEC CorporationThe Graduate School for the Creation of New Photonics IndustriesSYSTEC CorporationGraduate School of Interdisciplinary Science and Engineering in Health Systems, Okayama UniversityAbstract Artificial lipid bilayer single-channel recording technique has been employed to determine the biophysical and pharmacological properties of various ion channels. However, its measurement efficiency is very low, as it requires two time-consuming processes: preparation of lipid bilayer membranes and incorporation of ion channels into the membranes. In order to address these problems, we previously developed a technique based on hydrophilically modified gold probes on which are immobilized ion channels that can be promptly incorporated into the bilayer membrane at the same time as the membrane is formed on the probes’ hydrophilic area. Here, we improved further this technique by optimizing the gold probe and developed an automated channel current measurement system. We found that use of probes with rounded tips enhanced the efficiency of channel current measurements, and introducing a hydrophobic area on the probe surface, beside the hydrophilic one, further increased measurement efficiency by boosting membrane stability. Moreover, we developed an automated measurement system using the optimized probes; it enabled us to automatically measure channel currents and analyze the effects of a blocker on channel activity. Our study will contribute to the development of high-throughput devices to identify drug candidates affecting ion channel activity.https://doi.org/10.1038/s41598-021-97237-z
collection DOAJ
language English
format Article
sources DOAJ
author Minako Hirano
Masahisa Tomita
Chikako Takahashi
Nobuyuki Kawashima
Toru Ide
spellingShingle Minako Hirano
Masahisa Tomita
Chikako Takahashi
Nobuyuki Kawashima
Toru Ide
Development of an automated system to measure ion channel currents using a surface-modified gold probe
Scientific Reports
author_facet Minako Hirano
Masahisa Tomita
Chikako Takahashi
Nobuyuki Kawashima
Toru Ide
author_sort Minako Hirano
title Development of an automated system to measure ion channel currents using a surface-modified gold probe
title_short Development of an automated system to measure ion channel currents using a surface-modified gold probe
title_full Development of an automated system to measure ion channel currents using a surface-modified gold probe
title_fullStr Development of an automated system to measure ion channel currents using a surface-modified gold probe
title_full_unstemmed Development of an automated system to measure ion channel currents using a surface-modified gold probe
title_sort development of an automated system to measure ion channel currents using a surface-modified gold probe
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-09-01
description Abstract Artificial lipid bilayer single-channel recording technique has been employed to determine the biophysical and pharmacological properties of various ion channels. However, its measurement efficiency is very low, as it requires two time-consuming processes: preparation of lipid bilayer membranes and incorporation of ion channels into the membranes. In order to address these problems, we previously developed a technique based on hydrophilically modified gold probes on which are immobilized ion channels that can be promptly incorporated into the bilayer membrane at the same time as the membrane is formed on the probes’ hydrophilic area. Here, we improved further this technique by optimizing the gold probe and developed an automated channel current measurement system. We found that use of probes with rounded tips enhanced the efficiency of channel current measurements, and introducing a hydrophobic area on the probe surface, beside the hydrophilic one, further increased measurement efficiency by boosting membrane stability. Moreover, we developed an automated measurement system using the optimized probes; it enabled us to automatically measure channel currents and analyze the effects of a blocker on channel activity. Our study will contribute to the development of high-throughput devices to identify drug candidates affecting ion channel activity.
url https://doi.org/10.1038/s41598-021-97237-z
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