Key result
Recent advances in electrophysiological technologies, such as automated patch clamp and multi-electrode arrays, enable direct, label-free, high-throughput screening of ion channel function.
Automated patch clamp and multi-electrode array technologies provide advanced, higher-throughput methods for screening ion channel-targeting drugs and assessing cardiac safety.
May accelerate preclinical ion channel screening; extends research tools but leaves clinical translation open.
Ion channels are integral membrane proteins that regulate the flux of ions across the cell membrane. They are involved in nearly all physiological processes, and malfunction of ion channels has been linked to many diseases. Until recently, high-throughput screening of ion channels was limited to indirect, e.g. fluorescence-based, readout technologies. In the past years, direct label-free biophysical readout technologies by means of electrophysiology have been developed. Planar patch-clamp electrophysiology provides a direct functional label-free readout of ion channel function in medium to high throughput. Further electrophysiology features, including temperature control and higher-throughput instruments, are continually being developed. Electrophysiological screening in a 384-well format has recently become possible. Advances in chip and microfluidic design, as well as in cell preparation and handling, have allowed challenging cell types to be studied by automated patch clamp. Assays measuring action potentials in stem cell-derived cardiomyocytes, relevant for cardiac safety screening, and neuronal cells, as well as a large number of different ion channels, including fast ligand-gated ion channels, have successfully been established by automated patch clamp. Impedance and multi-electrode array measurements are particularly suitable for studying cardiomyocytes and neuronal cells within their physiological network, and to address more complex physiological questions. This article discusses recent advances in electrophysiological technologies available for screening ion channel function and regulation.
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Obergrussberger et al. (2015) reported a review. Electrophysiological screening technologies was evaluated. Recent advances in electrophysiological technologies, such as automated patch clamp and multi-electrode arrays, enable direct, label-free, high-throughput screening of ion channel function.
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