Evidence map›Paper›PMID 17261840›Full record

ArticleThe Journal of general physiology2007

Gating and inward rectifying properties of the MthK K+ channel with and without the gating ring.

Yang Li, Ian Berke, Liping Chen, Youxing Jiang

Abstract read
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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 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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  5. Article
  6. Forces and energetics of the canonical tetrameric cation channel gating.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Selectivity filter ion binding affinity determines inactivation in a potassium channel.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Polyamine block of MthK potassium channels.The Journal of general physiology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Stopped-Flow Fluorometric Ion Flux Assay for Ligand-Gated Ion Channel Studies.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Yang LiDepartment of Physiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Ian Berke
Liping Chen
Youxing Jiang

Funding

Mechanism of Ligand Gating in Potassium ChannelsR01GM071621 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI JIANG, YOUXING · 2004 to 2008
$1.4M
NIGMS NIH HHS GM071621NIGMS NIH HHS R01 GM071621
6 · The paper itself

Abstract

In MthK, a Ca2+-gated K+ channel from Methanobacterium thermoautotrophicum, eight cytoplasmic RCK domains form an octameric gating ring that controls the intracellular gate of the ion conduction pore. The binding of Ca2+ ions to the RCK domains alters the conformation of the gating ring, thereby opening the gate. In the present study, we examined the Ca2+- and pH-regulated gating and the rectifying conduction properties of MthK at the single-channel level. The open probability (Po) of MthK exhibits a sigmoidal relationship with intracellular [Ca2+], and a Hill coefficient >1 is required to describe the dependence of Po on [Ca2+], suggesting cooperative Ca2+ activation of the channel. Additionally, intracellular Ca2+ also blocks the MthK pore in a voltage-dependent manner, rendering an apparently inwardly rectifying I-V relation. Intracellular pH has a dual effect on MthK gating. Below pH 7.5, the channel becomes insensitive to Ca2+. This occurs because the gating ring is structurally unstable at this pH and tends to disassemble (Ye, S., Y. Li, L. Chen, and Y. Jiang. 2006. Cell. 126:1161-1173). In contrast, above pH 7.5, a further increase in pH shifts the Po-[Ca2+] relation towards a lower Ca2+ concentration, augments Po at saturating [Ca2+], and activates the channel even in the absence of Ca2+. Channel activity is marked by bursts of rapid openings and closings separated by relatively longer interburst closings. The duration of interburst closing and the burst length are highly Ca2+ and pH dependent, whereas the kinetics of intraburst events is Ca2+ and pH independent. The rapid intraburst openings and closings are also observed with the isolated MthK pore lacking the attached intracellular gating ring. The fast kinetic events, independent of both Ca2+ and pH, therefore appear to be determined by processes occurring within the ion conduction pore, whereas the slow events reflect the gating process controlled by Ca2+ and pH through the gating ring.

Indexed as

Ion Channel GatingAllosteric RegulationArchaeal ProteinsCalciumCloning, MolecularHydrogen-Ion ConcentrationKineticsLipid BilayersMembrane PotentialsMethanobacteriumModels, BiologicalPotassium Channels, Calcium-ActivatedPotassium Channels, Inwardly RectifyingProtein ConformationProtein Structure, TertiaryProtein SubunitsArchaeal ProteinsCalciumLipid BilayersPotassium Channels, Calcium-ActivatedPotassium Channels, Inwardly RectifyingProtein Subunits

Identifiers

PMID17261840
PMCPMC2154359

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.