Finkel Alan, Wittel Andrew, Yang Naibo, Handran Shawn, Hughes Jan, Costantin James
Molecular Devices Corporation, Union City, California 94587, USA.
J Biomol Screen. 2006 Aug;11(5):488-96. doi: 10.1177/1087057106288050. Epub 2006 Jun 7.
Present whole-cell patch-clamp methodology has only moderate consistency and throughput, rendering impractical functional measurements on large numbers of ion channel ligands or on large numbers of unknown or mutant channel genes. In the population patch clamp (PPC) described herein, a single voltage-clamp amplifier sums the whole-cell currents from multiple cells at once, each sealed to a separate aperture in a planar substrate well. The resulting ensemble currents are more consistent from well to well, and the success rate for each recording attempt is >95%. The PPC was implemented by modifying the PatchPlate substrate and amplifiers in the IonWorks patch-clamp instrument. The increased data consistency and likelihood of a successful recording in each well, combined with 384-well measurements in parallel, allow the direct electrophysiological recording of thousands of ensemble ionic currents per day. Therapeutic groups in drug discovery programs require this order of throughput to screen directed compound libraries against ion channel targets. The potential for studying the function of large numbers of ion channel mutants may be realized with the technique. The procedure incorporates subtraction methods that correct for expected distortions and also reliably produces data that agree with previous patch-clamp studies.
目前的全细胞膜片钳方法只有适度的一致性和通量,使得对大量离子通道配体或大量未知或突变通道基因进行功能测量不切实际。在本文所述的群体膜片钳(PPC)中,单个电压钳放大器同时对多个细胞的全细胞电流进行求和,每个细胞被封接到平面基质孔中的一个单独小孔上。从一个孔到另一个孔,得到的总体电流更加一致,每次记录尝试的成功率>95%。PPC是通过对IonWorks膜片钳仪器中的PatchPlate基质和放大器进行改造来实现的。数据一致性的提高以及每个孔成功记录的可能性,再加上并行的384孔测量,使得每天能够直接电生理记录数千个总体离子电流。药物发现项目中的治疗组需要这种通量水平来针对离子通道靶点筛选定向化合物库。利用该技术可以实现研究大量离子通道突变体功能的潜力。该程序采用减法方法来校正预期的失真,并且还能可靠地产生与先前膜片钳研究一致的数据。