Dan A. Klaerke, Maria de los Angeles Tejada, Vibeke Grøsfjeld Christensen, Mette Lassen, Per Amstrup Pedersen, Kirstine Calloe
{"title":"Reconstitution and Electrophysiological Characterization of Ion Channels in Lipid Bilayers","authors":"Dan A. Klaerke, Maria de los Angeles Tejada, Vibeke Grøsfjeld Christensen, Mette Lassen, Per Amstrup Pedersen, Kirstine Calloe","doi":"10.1002/cpph.37","DOIUrl":null,"url":null,"abstract":"<p>Detergent-solubilized purified ion channels can be reconstituted into lipid bilayers for electrophysiological analysis. Traditionally, ion channels were inserted into vesicles and subsequently fused with planar “black lipid membranes” formed from lipids dissolved in a hydrophobic solvent such as decane. Provided in this article is a step-by-step guide to reconstitute purified ion channel proteins into giant unilamellar vesicles (GUVs). This procedure results in the formation of proteoliposomes that can be used for planar bilayer formation and electrophysiological characterization of single-channel currents. By using preformed GUVs it is possible to omit the membrane solvent. Compared to traditional preparations, the lipid bilayers formed from GUVs provide an environment that more closely resembles the native cell membrane. Also described is an alternate protocol that entails the production of planar lipid bilayers from GUVs onto which proteins in detergent are added. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":10871,"journal":{"name":"Current Protocols in Pharmacology","volume":"81 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpph.37","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpph.37","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 6
Abstract
Detergent-solubilized purified ion channels can be reconstituted into lipid bilayers for electrophysiological analysis. Traditionally, ion channels were inserted into vesicles and subsequently fused with planar “black lipid membranes” formed from lipids dissolved in a hydrophobic solvent such as decane. Provided in this article is a step-by-step guide to reconstitute purified ion channel proteins into giant unilamellar vesicles (GUVs). This procedure results in the formation of proteoliposomes that can be used for planar bilayer formation and electrophysiological characterization of single-channel currents. By using preformed GUVs it is possible to omit the membrane solvent. Compared to traditional preparations, the lipid bilayers formed from GUVs provide an environment that more closely resembles the native cell membrane. Also described is an alternate protocol that entails the production of planar lipid bilayers from GUVs onto which proteins in detergent are added. © 2018 by John Wiley & Sons, Inc.
脂质双分子层离子通道的重构与电生理表征
洗涤剂溶解的纯化离子通道可以重组成脂质双分子层进行电生理分析。传统上,离子通道被插入到囊泡中,随后与由溶解在疏水溶剂(如癸烷)中的脂质形成的平面“黑色脂质膜”融合。在这篇文章中提供了一步一步的指导,将纯化的离子通道蛋白重组成巨大的单层囊泡(guv)。这一过程导致蛋白质脂质体的形成,可用于平面双层的形成和单通道电流的电生理表征。通过使用预成型guv,可以省略膜溶剂。与传统制剂相比,由guv形成的脂质双分子层提供了更接近天然细胞膜的环境。还描述了一种替代方案,该方案需要从guv产生平面脂质双分子层,并将洗涤剂中的蛋白质添加到其上。©2018 by John Wiley &儿子,Inc。
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