High throughput ion-channel pharmacology: Planar-array-based voltage clamp

被引:62
作者
Kiss, L [1 ]
Bennett, PB
Uebele, VN
Koblan, KS
Kane, SA
Neagle, B
Schroeder, K
机构
[1] Merck Res Labs, Dept Mol Pharmacol, West Point, PA 19486 USA
[2] Essen Instruments, Ann Arbor, MI USA
关键词
D O I
10.1089/154065803321537845
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Technological advances often drive major breakthroughs in biology. Examples include PCR, automated DNA sequencing, confocal/single photon microscopy, AFM, and voltage/patch-clamp methods. The patch-clamp method, first described nearly 30 years ago, was a major technical achievement that permitted voltage-clamp analysis (membrane potential control) of ion channels in most cells and revealed a role for channels in unimagined areas. Because of the high information content, voltage clamp is the best way to study ion-channel function; however, throughput is too low for drug screening. Here we describe a novel breakthrough planar-array-based HT patch-clamp technology developed by Essen Instruments capable of voltage-clamping thousands of cells per day. This technology provides greater than two orders of magnitude increase in throughput compared with the traditional voltage-clamp techniques. We have applied this method to study the hERG K+ channel and to determine the pharmacological profile of QT prolonging drugs.
引用
收藏
页码:127 / 135
页数:9
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