Asymmetric Lipid Bilayers and Potassium Channels Embedded Therein in the Contact Bubble Bilayer
Authors:
- 11 June 2024
- book chapter
- Published by Springer Nature
- Vol. 2796, 1-21
Abstract
Cell membranes are highly intricate systems comprising numerous lipid species and membrane proteins, where channel proteins, lipid molecules, and lipid bilayers, as continuous elastic fabric, collectively engage in multi-modal interplays. Owing to the complexity of the native cell membrane, studying the elementary processes of channel–membrane interactions necessitates a bottom-up approach starting from forming simplified synthetic membranes. This is the rationale for establishing an in vitro membrane reconstitution system consisting of a lipid bilayer with a defined lipid composition and a channel molecule. Recent technological advancements have facilitated the development of asymmetric membranes, and the contact bubble bilayer (CBB) method allows single-channel current recordings under arbitrary lipid compositions in asymmetric bilayers. Here, we present an experimental protocol for the formation of asymmetric membranes using the CBB method. The KcsA potassium channel is a prototypical model channel with huge structural and functional information and thus serves as a reporter of membrane actions on the embedded channels. We demonstrate specific interactions of anionic lipids in the inner leaflet. Considering that the local lipid composition varies steadily in cell membranes, we `present a novel lipid perfusion technique that allows rapidly changing the lipid composition while monitoring the single-channel behavior. Finally, we demonstrate a leaflet perfusion method for modifying the composition of individual leaflets. These techniques with custom synthetic membranes allow for variable experiments, providing crucial insights into channel–membrane interplay in cell membranes.Keywords
This publication has 79 references indexed in Scilit:
- Engineering asymmetric vesiclesProceedings of the National Academy of Sciences, 2003
- Sequence-Function Analysis of the K+-Selective Family of Ion Channels Using a Comprehensive Alignment and the KcsA Channel StructureBiophysical Journal, 2003
- Effect of External pH on Activation of the Kv1.5 Potassium ChannelBiophysical Journal, 2003
- Surface Potentials and the Calculated Selectivity of Ion ChannelsBiophysical Journal, 2002
- Functional Reconstitution of a Prokaryotic K+ ChannelJournal of General Physiology, 1998
- Voltage-dependent gating of an asymmetric gramicidin channel.Proceedings of the National Academy of Sciences, 1995
- JPCalc, a software package for calculating liquid junction potential corrections in patch-clamp, intracellular, epithelial and bilayer measurements and for correcting junction potential measurementsJournal of Neuroscience Methods, 1994
- M2 delta, a candidate for the structure lining the ionic channel of the nicotinic cholinergic receptor.Proceedings of the National Academy of Sciences, 1988
- Voltage-dependent capacitance in lipid bilayers made from monolayersBiophysical Journal, 1978
- Formation of Bimolecular Membranes from Lipid Monolayers and a Study of Their Electrical PropertiesProceedings of the National Academy of Sciences, 1972