Study of TRP Channels by Automated Patch Clamp Systems

Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 704)


Ion channels are responsible for the permeation of ions across the membrane and their central role in cellular physiology is well established. Historically, the direct study of ion channels has been considered technically challenging. As such, a significant barrier to drug discovery for ion channels has been the low throughput of high quality electrophysiological data. The emergence of automated high throughput platforms for studying ion channel kinetics and pharmacology has lowered this barrier. Ion channels are now recognized as increasingly important drug targets and a diverse range of ion channels are implicated in a variety of drug discovery and cardiac safety assessment programs. The TRP (Transient Receptor Potential) superfamily of ion channels play a crucial role in a broad range of sensory functions including vision, taste, olfaction, hearing, touch, pain and thermosensation. Many of the TRP channels are polymodal in their activation and deactivation mechanisms and even with conventional patch clamp electrophysiology, the TRP channels are considered to be a very complex target class. Here we present an update on the significant progress made on the TRP receptor assays with the available automated patch clamp systems.


Transient Receptor Potential Patch Clamp Transient Receptor Potential Channel Trouble Asset Relief Program Patch Clamp Electrophysiology 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.



The QPatch results presented in this review have been generated by many scientists at Sophion Bioscience. We would especially like to thank Rikke L. Schrøder and Hervør L. Olsen for their contribution with data: Dorthe Nielsen is acknowledged for her expert technical assistance. M. Knirke Jensen and Søren Friis are thanked for providing data and valuable critical input to this manuscript. Many thanks also to Chris Mathes for being an inspirator and scientific mentor during both data and manuscript generation.

We thank AstraZeneca, Sweden, for generously proving the TRPA1, TRPV1, and TRPM8 cell lines. The scientists at Novartis, UK, Pamela Tranter, Mark McPate and Martin Gosling are thanked for sharing their data on TRPM2.


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Copyright information

© Springer Science+Business Media B.V. 2011

Authors and Affiliations

  1. 1.Sophion Bioscience ASBallerupDenmark

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