Filter gate closure inhibits ion but not water transport

Activity: Talk or presentationInvited talkunknown

Description

Filter gate closure inhibits ion but not water transport through potassium channels Torben Hoomann,1 Nadin Jahnke,2 Andreas Horner,1 Sandro Keller,2 Peter Pohl,1 1 Johannes Kepler University Linz, Institute of Biophysics, Linz, Austria 2 Molecular Biophysics, University of Kaiserslautern, Germany The selectivity filter of K+ channels is conserved throughout all kingdoms of life. Carbonyl groups of highly conserved amino acids point toward the lumen to act as surrogates for the water molecules of K+ hydration. Ion conductivity is abrogated if some of these carbonyl groups flip out of the lumen, which happens (i) in the process of C-type inactivation or (ii) during filter collapse in the absence of K+. Here, we show that K+ channels remain permeable to water even after entering such an electrically silent conformation. We reconstituted fluorescently labeled and constitutively open mutants of the bacterial K+ channel KcsA into lipid vesicles that were either C-type inactivating or non-inactivating. Fluorescence correlation spectroscopy allowed us to count both the number of proteoliposomes and the number of protein-containing micelles after solubilization, providing the number of reconstituted channels per proteoliposome. Quantification of the per-channel increment in proteoliposome water permeability with the aid of stopped-flow experiments yielded a unitary water permeability pf of (6.9±0.6)x10-13cm3s-1 for both mutants. “Collapse” of the selectivity filter upon K+ removal did not alter pf and was fully reversible, as demonstrated by current measurements through planar bilayers in a K+-containing medium to which K+-free proteoliposomes were fused. Water flow through KcsA is halved by 200 mM K+ in the aqueous solution, which indicates an effective K+ dissociation constant in that range for a singly occupied channel. This questions the widely accepted hypothesis that multiple K+ ions in the selectivity filter act to mutually destabilize binding
Period30 Jul 2013
Event title541. WE-Heraeus-Seminar: Transport through Nanopores: From Understanding to Engineering
Event typeConference
LocationGermanyShow on map

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