ArticleThe Journal of general physiology2007
A direct demonstration of closed-state inactivation of K+ channels at low pH.
Article in The Journal of general physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
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Who cites it
22 citing papers in PubMed.
- The activation gate controls steady-state inactivation and recovery from inactivation in Shaker.The Journal of general physiology · 2020Article
- Article
- Article
- Regulation of human cardiac Kv1.5 channels by extracellular acidification.Pflugers Archiv : European journal of physiology · 2016Article
- A Disease Mutation Causing Episodic Ataxia Type I in the S1 Links Directly to the Voltage Sensor and the Selectivity Filter in Kv Channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015Article
- Kinetic model for NS1643 drug activation of WT and L529I variants of Kv11.1 (hERG1) potassium channel.Biophysical journal · 2015Article
- Components of gating charge movement and S4 voltage-sensor exposure during activation of hERG channels.The Journal of general physiology · 2013Article
- Voltage sensor inactivation in potassium channels.Frontiers in pharmacology · 2012Article
- Mechanisms of closed-state inactivation in voltage-gated ion channels.The Journal of physiology · 2011Review
- Mutations within the S4-S5 linker alter voltage sensor constraints in hERG K+ channels.Biophysical journal · 2010Article
- Biophysical characterization of the fluorescent protein voltage probe VSFP2.3 based on the voltage-sensing domain of Ci-VSP.European biophysics journal : EBJ · 2010Article
- Kinetic analysis of the effects of H+ or Ni2+ on Kv1.5 current shows that both ions enhance slow inactivation and induce resting inactivation.The Journal of physiology · 2010Article
- Fast and slow voltage sensor rearrangements during activation gating in Kv1.2 channels detected using tetramethylrhodamine fluorescence.The Journal of general physiology · 2010Article
- Fluorescence-tracking of activation gating in human ERG channels reveals rapid S4 movement and slow pore opening.PloS one · 2010Article
- Coupling of activation and inactivation gate in a K+-channel: potassium and ligand sensitivity.The EMBO journal · 2009Article
- External Ba2+ block of human Kv1.5 at neutral and acidic pH: evidence for Ho+-induced constriction of the outer pore mouth at rest.Biophysical journal · 2008Article
- Effects of changes in extracellular pH and potassium concentration on Kv1.3 inactivation.European biophysics journal : EBJ · 2008Article
- Voltage clamp fluorimetry reveals a novel outer pore instability in a mammalian voltage-gated potassium channel.The Journal of general physiology · 2008Article
- Gating charge immobilization in Kv4.2 channels: the basis of closed-state inactivation.The Journal of general physiology · 2008Article
- Mechanism of the modulation of Kv4:KChIP-1 channels by external K+.Biophysical journal · 2008Article
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Lowering external pH reduces peak current and enhances current decay in Kv and Shaker-IR channels. Using voltage-clamp fluorimetry we directly determined the fate of Shaker-IR channels at low pH by measuring fluorescence emission from tetramethylrhodamine-5-maleimide attached to substituted cysteine residues in the voltage sensor domain (M356C to R362C) or S5-P linker (S424C). One aspect of the distal S3-S4 linker alpha-helix (A359C and R362C) reported a pH-induced acceleration of the slow phase of fluorescence quenching that represents P/C-type inactivation, but neither site reported a change in the total charge movement at low pH. Shaker S424C fluorescence demonstrated slow unquenching that also reflects channel inactivation and this too was accelerated at low pH. In addition, however, acidic pH caused a reversible loss of the fluorescence signal (pKa = 5.1) that paralleled the reduction of peak current amplitude (pKa = 5.2). Protons decreased single channel open probability, suggesting that the loss of fluorescence at low pH reflects a decreased channel availability that is responsible for the reduced macroscopic conductance. Inhibition of inactivation in Shaker S424C (by raising external K(+) or the mutation T449V) prevented fluorescence loss at low pH, and the fluorescence report from closed Shaker ILT S424C channels implied that protons stabilized a W434F-like inactivated state. Furthermore, acidic pH changed the fluorescence amplitude (pKa = 5.9) in channels held continuously at -80 mV. This suggests that low pH stabilizes closed-inactivated states. Thus, fluorescence experiments suggest the major mechanism of pH-induced peak current reduction is inactivation of channels from closed states from which they can activate, but not open; this occurs in addition to acceleration of P/C-type inactivation from the open state.
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