Article
Four drug-sensitive subunits are required for maximal effect of a voltage sensor-targeted KCNQ opener.
The Journal of general physiology - 1 Oct 2018
Wang Alice W, Yau Michael C, Wang Caroline K, Sharmin Nazlee, Yang Runying Y, Pless Stephan A, Kurata Harley T
Abstract excerpt
KCNQ2-5 (Kv7.2-Kv7.5) channels are strongly influenced by an emerging class of small-molecule channel activators. Retigabine is the prototypical KCNQ activator that is thought to bind within the pore. It requires the presence of a Trp side chain that is conserved among retigabine-sensitive channels but absent in the retigabine-insensitive KCNQ1 subtype. Recent work has demonstrated that certain KCNQ openers are...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
