PubMed 19435843
Referenced in: none
Automatically associated channels: Slo1
Title: Molecular recognition and self-assembly special feature: Calix[4]arene-based conical-shaped ligands for voltage-dependent potassium channels.
Authors: Vera Martos, Sarah C Bell, Eva Santos, Ehud Y Isacoff, Dirk Trauner, Javier de Mendoza
Journal, date & volume: Proc. Natl. Acad. Sci. U.S.A., 2009 Jun 30 , 106, 10482-6
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/19435843
Abstract
Potassium channels are among the core functional elements of life because they underpin essential cellular functions including excitability, homeostasis, and secretion. We present here a series of multivalent calix[4]arene ligands that bind to the surface of voltage-dependent potassium channels (K(v)1.x) in a reversible manner. Molecular modeling correctly predicts the best candidates with a conical C(4) symmetry for optimal binding, and the effects on channel function are assessed electrophysiologically. Reversible inhibition was observed, without noticeable damage of the oocytes, for tetraacylguanidinium or tetraarginine members of the series with small lower rim O-substituents. Apparent binding constants were in the low micromolar range and had Hill coefficients of 1, consistent with a single site of binding. Suppression of current amplitude was accompanied by a positive shift in the voltage dependence of gating and slowing of both voltage sensor motion and channel opening. These effects are in keeping with expectations for docking in the central pore and interaction with the pore domain "turret."