Screening ion-channel ligand interactions with passive pumping in a microfluidic bilayer lipid membrane chip

被引:4
|
作者
Saha, Shimul C. [1 ,2 ]
Powl, Andrew M. [3 ]
Wallace, B. A. [3 ]
de Planque, Maurits R. R. [1 ,2 ]
Morgan, Hywel [1 ,2 ]
机构
[1] Univ Southampton, Elect & Comp Sci, Southampton SO17 1BJ, Hants, England
[2] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, Hants, England
[3] Univ London Birkbeck Coll, Inst Struct & Mol Biol, London WC1E 7HX, England
来源
BIOMICROFLUIDICS | 2015年 / 9卷 / 01期
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
POTASSIUM CHANNEL; SOLUTION EXCHANGE; KCSA; APERTURES; TETRAETHYLAMMONIUM; RECORDINGS; MICROARRAY; RESOLUTION; STABILITY; NANOPORES;
D O I
10.1063/1.4905313
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a scalable artificial bilayer lipid membrane platform for rapid electrophysiological screening of ion channels and transporters. A passive pumping method is used to flow microliter volumes of ligand solution across a suspended bilayer within a microfluidic chip. Bilayers are stable at flow rates up to similar to 0.5 mu l/min. Phospholipid bilayers are formed across a photolithographically defined aperture made in a dry film resist within the microfluidic chip. Bilayers are stable for many days and the low shunt capacitance of the thin film support gives lownoise high-quality single ion channel recording. Dose-dependent transient blocking of alpha-hemolysin with beta-cyclodextrin (beta-CD) and polyethylene glycol is demonstrated and dose-dependent blocking studies of the KcsA potassium channel with tetraethylammonium show the potential for determining IC50 values. The assays are fast (30 min for a complete IC50 curve) and simple and require very small amounts of compounds (100 mu g in 15 mu l). The technology can be scaled so that multiple bilayers can be addressed, providing a screening platform for ion channels, transporters, and nanopores. (c) 2015 AIP Publishing LLC.
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页数:11
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