Referenced in: none

Automatically associated channels: Kir2.1 , Kv11.1 , Nav1.7

Title: Automated Patch Clamp Meets High-Throughput Screening: 384 Cells Recorded in Parallel on a Planar Patch Clamp Module.

Authors: Alison Obergrussberger, Andrea Brüggemann, Tom A Goetze, Markus Rapedius, Claudia Haarmann, Ilka Rinke, Nadine Becker, Takayuki Oka, Atsushi Ohtsuki, Timo Stengel, Marius Vogel, Juergen Steindl, Max Mueller, Johannes Stiehler, Michael George, Niels Fertig

Journal, date & volume: J Lab Autom, 2015 Dec 23 , ,

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26702021

Abstract
We have developed an automated patch clamp module for high-throughput ion channel screening, recording from 384 cells simultaneously. The module is incorporated into a laboratory pipetting robot and uses a 384-channel pipettor head for application of cells and compounds. The module contains 384 amplifier channels for fully parallel recordings using a digital amplifier. Success rates for completed experiments (1- to 4-point concentration-response curves for cells satisfying defined quality control parameters) of greater than 85% have been routinely achieved with, for example, HEK, CHO, and RBL cell lines expressing hNaV1.7, hERG, Kir2.1, GABA, or glutamate receptors. Pharmacology experiments are recorded and analyzed using specialized software, and the pharmacology of hNaV1.7 and hERG is described. Fast external solution exchange rates of <50 ms are demonstrated using Kir2.1. Short exposure times are achieved by stacking the external solutions inside the pipette of the robot to minimize exposure of the ligand on the receptor. This ensures that ligand-gated ion channels, for example, GABA and glutamate described in this report, can be reproducibly recorded. Stem cell-derived cardiomyocytes have also been used with success rates of 52% for cells that have a seal resistance of >200 MΩ, and recordings of voltage-gated Na+ and Ca2+ are shown.