Lipid bilayer technologies in ion channel recordings and their potential in drug screening assay

被引:42
作者
Kongsuphol, Patthara [1 ]
Fang, Kok Boon [1 ]
Ding, Zhipeng [1 ]
机构
[1] Inst Microelect, Singapore 117685, Singapore
关键词
Lipid bilayer; BLM; Ion channels; Drug screening; Lab-on-a-Chip; LOC; ON-A-CHIP; SUPPORTED MEMBRANES; GRAMICIDIN CHANNELS; IMPEDANCE ANALYSIS; POTASSIUM CHANNEL; IN-VITRO; SILICON; RECONSTITUTION; PROTEIN; ELECTROPHYSIOLOGY;
D O I
10.1016/j.snb.2013.04.119
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ion channels are expressed in every tissue and are important for many physiological processes. Malfunction of ion channels can lead to diseases in many tissues. All these make ion channels ideal targets for drug development. Many techniques are employed to study ion channel functions including the lipid bilayer technique. Lipid bilayer membranes are being synthesized in vitro to mimic natural cell membranes. Ion channels are then incorporated into the bilayer membrane for ion channels activity recordings. The use of Lab-on-a-Chip (LOC) technologies to form lipid bilayer has made lipid bilayer technique efficient for ion channel recordings and has brought great potential for this technique to be scaled up to a high throughput platform for ion channel drug screening. In this review we discuss the use of lipid bilayer for ion channel studies, conventional methods and current LOC technologies on lipid bilayer formations, comparison of lipid bilayer high throughput platform to automated patch clamp system, and finally the potential of lipid bilayer platforms in drug screening assay. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:530 / 542
页数:13
相关论文
共 108 条
[1]  
Adams M., 2010, NATURE ED, V3, P20
[2]   Voltage-induced gating of the mechanosensitive MscL ion channel reconstituted in a tethered lipid bilayer membrane [J].
Andersson, Martin ;
Okeyo, George ;
Wilson, Danyell ;
Keizer, Henk ;
Moe, Paul ;
Blount, Paul ;
Fine, Daniel ;
Dodabalapur, Ananth ;
Duran, Randolph S. .
BIOSENSORS & BIOELECTRONICS, 2008, 23 (06) :919-923
[3]   Detection of single ion channel activity on a chip using tethered bilayer membranes [J].
Andersson, Martin ;
Keizer, Henk M. ;
Zhu, Chenyu ;
Fine, Daniel ;
Dodabalapur, Ananth ;
Duran, Randolph S. .
LANGMUIR, 2007, 23 (06) :2924-2927
[4]   Ircinialactams: Subunit-selective glycine receptor modulators from Australian sponges of the family Irciniidae [J].
Balansa, Walter ;
Islam, Robiul ;
Fontaine, Frank ;
Piggott, Andrew M. ;
Zhang, Hua ;
Webb, Timothy I. ;
Gilbert, Daniel F. ;
Lynch, Joseph W. ;
Capon, Robert J. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2010, 18 (08) :2912-2919
[5]   TEMPERATURE-DEPENDENT PROPERTIES OF GRAMICIDIN A CHANNELS [J].
BAMBERG, E ;
LAUGER, P .
BIOCHIMICA ET BIOPHYSICA ACTA, 1974, 367 (02) :127-133
[6]   Droplet interface bilayers [J].
Bayley, Hagan ;
Cronin, Brid ;
Heron, Andrew ;
Holden, Matthew A. ;
Hwang, William L. ;
Syeda, Ruhma ;
Thompson, James ;
Wallace, Mark .
MOLECULAR BIOSYSTEMS, 2008, 4 (12) :1191-1208
[7]   DISCRETE CONDUCTANCE FLUCTUATIONS IN LIPID BILAYER PROTEIN MEMBRANES [J].
BEAN, RC ;
SHEPHERD, WC ;
CHAN, H ;
EICHNER, J .
JOURNAL OF GENERAL PHYSIOLOGY, 1969, 53 (06) :741-&
[8]   Matrix Mg2+ regulates mitochondrial ATP-dependent potassium channel from heart [J].
Bednarezyk, P ;
Dolowy, K ;
Szewczyk, A .
FEBS LETTERS, 2005, 579 (07) :1625-1632
[9]   Expression and functional characterization of the cardiac muscle ryanodine receptor Ca2+ release channel in Chinese hamster ovary cells [J].
Bhat, MB ;
Hayek, SM ;
Zhao, JY ;
Zang, WJ ;
Takeshima, H ;
Wier, WG ;
Ma, JJ .
BIOPHYSICAL JOURNAL, 1999, 77 (02) :808-816
[10]   Hit and lead generation:: Beyond high-throughput screening [J].
Bleicher, KH ;
Böhm, HJ ;
Müller, K ;
Alanine, AI .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (05) :369-378