Sequential interaction of chloride and proton ions with the fast gate steer the voltage-dependent gating in ClC-2 chloride channels
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The interaction of either H%2b or Cl- ions with the fast gate is the major source of voltage (Vm) dependence in ClC Cl- channels. However, the mechanism by which these ions confer Vm dependence to the ClC-2 Cl- channel remains unclear. By determining the Vm dependence of normalized conductance (Gnorm(Vm)), an index of open probability, ClC-2 gating was studied at different [H%2b]i, [H%2b]o and [Cl-]i. Changing [H%2b]i by five orders of magnitude whilst [Cl-]i/[Cl-]o= 140/140 or 10/140 mm slightly shifted Gnorm(Vm) to negative Vm without altering the onset kinetics; however, channel closing was slower at acidic pHi. A similar change in [H%2b]o with [Cl-]i/[Cl-]o= 140/140 mm enhanced Gnorm in a bell-shaped manner and shifted Gnorm(Vm) curves to positive Vm. Importantly, Gnorm was >0 with [H%2b]o= 10-10m but channel closing was slower when [H%2b]o or [Cl-]i increased implying that ClC-2 was opened without protonation and that external H%2b and/or internal Cl- ions stabilized the open conformation. The analysis of kinetics and steady-state properties at different [H%2b]o and [Cl-]i was carried out using a gating Scheme coupled to Cl- permeation. Unlike previous results showing Vm-dependent protonation, our analysis revealed that fast gate protonation was Vm and Cl- independent and the equilibrium constant for closed-open transition of unprotonated channels was facilitated by elevated [Cl-]i in a Vm-dependent manner. Hence a Vm dependence of pore occupancy by Cl- induces a conformational change in unprotonated closed channels, before the pore opens, and the open conformation is stabilized by Cl- occupancy and Vm-independent protonation. © 2012 The Authors. The Journal of Physiology © 2012 The Physiological Society.
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chloride channel; chloride channel CIC 2; chloride ion; proton; unclassified drug; acidity; article; binding site; cell membrane potential; channel gating; chloride conductance; conformational transition; controlled study; equilibrium constant; molecular interaction; molecular stability; pH measurement; priority journal; proton transport; signal transduction; steady state; Animals; Chloride Channels; Chlorides; Electrophysiological Phenomena; HEK293 Cells; Humans; Hydrogen-Ion Concentration; Ion Channel Gating; Kinetics; Mice; Models, Biological; Protein Conformation; Protons; Recombinant Proteins
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