Cholesterol binding to ion channels

Numerous studies demonstrated that membrane cholesterol is a major regulator of ion channel function. The goal of this review is to discuss significant advances that have been recently achieved in elucidating the mechanisms responsible for cholesterol regulation of ion channels. The first major insi...

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Main Authors: Irena eLevitan, Dev K Singh, Avia eRosenhouse-Dantsker
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-02-01
Series:Frontiers in Physiology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fphys.2014.00065/full
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spelling doaj-7697ef4ebc8a4e22996305787c439b512020-11-24T22:36:39ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2014-02-01510.3389/fphys.2014.0006578002Cholesterol binding to ion channelsIrena eLevitan0Dev K Singh1Avia eRosenhouse-Dantsker2University of Illinois at ChicagoUniversity of Illinois at ChicagoUniversity of Illinois at ChicagoNumerous studies demonstrated that membrane cholesterol is a major regulator of ion channel function. The goal of this review is to discuss significant advances that have been recently achieved in elucidating the mechanisms responsible for cholesterol regulation of ion channels. The first major insight that comes from growing number of studies that based on the sterol specificity of cholesterol effects, show that several types of ion channels (nAChR, Kir, BK, TRPV) are regulated by specific sterol-protein interactions. This conclusion is supported by demonstrating direct saturable binding of cholesterol to a bacterial Kir channel. The second major advance in the field is the identification of putative cholesterol binding sites in several types of ion channels. These include sites at locations associated with the well-known cholesterol binding motif CRAC and its reversed form CARC in nAChR, BK, and TRPV, as well as novel cholesterol binding regions in Kir channels. Notably, in the majority of these channels, cholesterol is suggested to interact mainly with hydrophobic residues in non-annular regions of the channels being embedded in between transmembrane protein helices. We also discuss how identification of putative cholesterol binding sites is an essential step to understand the mechanistic basis of cholesterol-induced channel regulation. Clearly, however, these are only the first few steps in obtaining a general understanding of cholesterol-ion channels interactions and their roles in cellular and organ functions.http://journal.frontiersin.org/Journal/10.3389/fphys.2014.00065/fullCholesterolIon ChannelsLipidsMembrane Proteinscholesterol-binding motifs
collection DOAJ
language English
format Article
sources DOAJ
author Irena eLevitan
Dev K Singh
Avia eRosenhouse-Dantsker
spellingShingle Irena eLevitan
Dev K Singh
Avia eRosenhouse-Dantsker
Cholesterol binding to ion channels
Frontiers in Physiology
Cholesterol
Ion Channels
Lipids
Membrane Proteins
cholesterol-binding motifs
author_facet Irena eLevitan
Dev K Singh
Avia eRosenhouse-Dantsker
author_sort Irena eLevitan
title Cholesterol binding to ion channels
title_short Cholesterol binding to ion channels
title_full Cholesterol binding to ion channels
title_fullStr Cholesterol binding to ion channels
title_full_unstemmed Cholesterol binding to ion channels
title_sort cholesterol binding to ion channels
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2014-02-01
description Numerous studies demonstrated that membrane cholesterol is a major regulator of ion channel function. The goal of this review is to discuss significant advances that have been recently achieved in elucidating the mechanisms responsible for cholesterol regulation of ion channels. The first major insight that comes from growing number of studies that based on the sterol specificity of cholesterol effects, show that several types of ion channels (nAChR, Kir, BK, TRPV) are regulated by specific sterol-protein interactions. This conclusion is supported by demonstrating direct saturable binding of cholesterol to a bacterial Kir channel. The second major advance in the field is the identification of putative cholesterol binding sites in several types of ion channels. These include sites at locations associated with the well-known cholesterol binding motif CRAC and its reversed form CARC in nAChR, BK, and TRPV, as well as novel cholesterol binding regions in Kir channels. Notably, in the majority of these channels, cholesterol is suggested to interact mainly with hydrophobic residues in non-annular regions of the channels being embedded in between transmembrane protein helices. We also discuss how identification of putative cholesterol binding sites is an essential step to understand the mechanistic basis of cholesterol-induced channel regulation. Clearly, however, these are only the first few steps in obtaining a general understanding of cholesterol-ion channels interactions and their roles in cellular and organ functions.
topic Cholesterol
Ion Channels
Lipids
Membrane Proteins
cholesterol-binding motifs
url http://journal.frontiersin.org/Journal/10.3389/fphys.2014.00065/full
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AT devksingh cholesterolbindingtoionchannels
AT aviaerosenhousedantsker cholesterolbindingtoionchannels
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