Isoform-specific prolongation of Kv7 (KCNQ) potassium channel opening mediated by new molecular determinants for drug-channel interactions

Gao, Z., Zhang, T., Wu, M., Xiong, Q., Sun, H., Zhang, Y., Zu, L., Wang, W., Li, M. (June 2010) Isoform-specific prolongation of Kv7 (KCNQ) potassium channel opening mediated by new molecular determinants for drug-channel interactions. Journal of Biological Chemistry, 285 (36). pp. 28322-28332.

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URL: http://www.ncbi.nlm.nih.gov/pubmed/20584905
DOI: 10.1074/jbc.M110.116392

Abstract

Kv7 channels, especially Kv7.2 (KCNQ2) and Kv7.3 (KCNQ3), are key determinants for membrane excitability in the brain. Some chemical modulators of KCNQ channels are in development for use as anti-epileptic drugs, such as retigabine (D-23129, N-(2-amino-4-(4-fluorobenzylamino)-phenyl)), which was recently approved for clinical use. In addition, several other compounds were also reported to potentiate activity of the Kv7 channels. It is therefore of interest to investigate compound-channel interactions, so that more insights may be gained to aid future development of therapeutics. We have conducted a screen of 20,000 compounds for KCNQ2 potentiators using rubidium flux combined with atomic absorption spectrometry. Here, we report the characterization of a series of new structures that display isoform specificity and induce a marked reduction of deactivation distinct from that of retigabine. Furthermore, KCNQ2(W236L), a previously reported mutation that abolishes sensitivity to retigabine, remains fully sensitive to these compounds. This result, together with mutagenesis and other studies, suggests that the reported compounds confer a unique mode of action and involve new molecular determinants on the channel protein, consistent with the idea of recognizing a new site on channel protein. © 2010 by The American Society for Biochemistry and Molecular Biology, Inc.

Item Type: Paper
Subjects: Investigative techniques and equipment > spectroscopy > atomic absorption spectrometry
organs, tissues, organelles, cell types and functions > organs types and functions > brain
CSHL Authors:
Communities: CSHL Post Doctoral Fellows
CSHL labs > Zador lab
Depositing User: CSHL Librarian
Date: 28 June 2010
Date Deposited: 30 Sep 2011 14:23
Last Modified: 03 May 2013 15:51
PMCID: PMC2934696
Related URLs:
URI: http://repository.cshl.edu/id/eprint/15419

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