Pehl Ulrich, Leisgen Christine, Gampe Kristine, Guenther Elke
NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
Assay Drug Dev Technol. 2004 Oct;2(5):515-24. doi: 10.1089/adt.2004.2.515.
As numerous diseases have been shown to be related to dysfunction of ion channels and neurotransmitter receptors and to affect regulatory pathways, ion channels have attracted increasing attention as a target class for drug discovery. The concomitant demand of the pharmaceutical industry for adequate electrophysiological methods to investigate drug effects on specific ion channels in secondary and safety screening has resulted in the development of electrophysiological instrumentation that allows automated monitoring of ion channel function with a higher throughput. Here we tested a fully automated screening system based on the Xenopus laevis oocyte expression system. We addressed the questions of data quality and reproducibility obtained by automated oocyte injection and two-electrode voltage-clamp (TEVC) recording using the Roboocyte (Multi Channel Systems GmbH, Reutlingen, Germany) technology compared to conventional oocyte recording. A gamma-aminobutyric acid (GABA)A-receptor subtype (alpha(1)beta(2)) was chosen as an example for a ligand-gated ion channel, and the slowly activating potassium current I(Ks) as a voltage-activated ion channel. Oocytes were injected with cDNA or cRNA via the Roboocyte injection stage. Ion channel currents were successfully recorded after 2-7 days in about 40% of the oocytes injected with GABA(A) receptor cDNA, and after 2-4 days in about 60% of the oocytes injected with KCNE1 cRNA. EC(50) values for the GABA(A) receptor and IC(50) values for blockers of I(Ks) were comparable to values obtained with conventional TEVC recording techniques. In conclusion, our results show that the Roboocyte is a valuable automated tool for oocyte injection and TEVC recording that can be used in drug screening and target validation to enhance the number of compounds and oocytes tested per day.
由于众多疾病已被证明与离子通道和神经递质受体功能障碍有关,并会影响调节途径,离子通道作为药物发现的一类靶点已引起越来越多的关注。制药行业对用于在二级筛选和安全性筛选中研究药物对特定离子通道作用的适当电生理方法的相应需求,导致了电生理仪器的发展,该仪器能够以更高的通量自动监测离子通道功能。在此,我们测试了一种基于非洲爪蟾卵母细胞表达系统的全自动筛选系统。我们探讨了与传统卵母细胞记录相比,使用Roboocyte(德国罗伊特林根的多通道系统有限公司)技术进行自动卵母细胞注射和双电极电压钳(TEVC)记录所获得的数据质量和可重复性问题。选择γ-氨基丁酸(GABA)A受体亚型(α(1)β(2))作为配体门控离子通道的示例,以及缓慢激活的钾电流I(Ks)作为电压激活离子通道的示例。通过Roboocyte注射平台将cDNA或cRNA注射到卵母细胞中。在注射GABA(A)受体cDNA的约40%的卵母细胞中,2 - 7天后成功记录到离子通道电流;在注射KCNE1 cRNA的约60%的卵母细胞中,2 - 4天后成功记录到离子通道电流。GABA(A)受体的半数有效浓度(EC(50))值和I(Ks)阻滞剂的半数抑制浓度(IC(50))值与使用传统TEVC记录技术获得的值相当。总之,我们的结果表明,Roboocyte是用于卵母细胞注射和TEVC记录的有价值的自动化工具,可用于药物筛选和靶点验证,以增加每天测试的化合物和卵母细胞数量。