Evidence map›Paper›PMID 16043772›Full record

ArticleThe Journal of general physiology2005

K channel subconductance levels result from heteromeric pore conformations.

Mark L Chapman, Antonius M J VanDongen

Abstract readComparative Study
In one paragraph

Article in The Journal of general physiology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

43 citing papers in PubMed.

  1. Multiple Conductance States in Artificial Unimolecular Channels.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  2. Article
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  5. Article
  6. Article
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  9. Review
  10. Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  11. The tarantula toxin GxTx detains KThe Journal of general physiology · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Modeling ion channels: past, present, and future.The Journal of general physiology · 2014
    Review
  18. Single-channel basis for the slow activation of the repolarizing cardiac potassium current, I(Ks).Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Mark L ChapmanDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA.
Antonius M J VanDongen

Funding

The Molecular Basis of Ion Channel OpeningR01NS031557 · NINDS · DUKE UNIVERSITY · PI VANDONGEN, ANTONIUS M · 1993 to 2004
$1.3M
NINDS NIH HHS 5R01 NS 031557-12NINDS NIH HHS R01 NS031557
6 · The paper itself

Abstract

Voltage-gated K channels assemble from four identical subunits symmetrically arranged around a central permeation pathway. Each subunit harbors a voltage-sensing domain. The sigmoidal nature of the activation kinetics suggests that multiple sensors need to undergo a conformational change before the channel can open. Following activation, individual K channels alternate stochastically between two main permeation states, open and closed. This binary character of single channel behavior suggests the presence of a structure in the permeation pathway that can exist in only two conformations. However, single channel analysis of drk1 (K(v)2.1) K channels demonstrated the existence of four additional, intermediate conductance levels. These short-lived subconductance levels are visited when the channel gate moves between the closed and fully open state. We have proposed that these sublevels arise from transient heteromeric pore conformations, in which some, but not all, subunits are in the "open" state. A minimal model based on this hypothesis relates specific subconductance states with the number of activated subunits (Chapman et al., 1997). To stringently test this hypothesis, we constructed a tandem dimer that links two K channel subunits with different activation thresholds. Activation of this dimer by strong depolarizations resulted in the characteristic binary open-close behavior. However, depolarizations to membrane potentials in between the activation thresholds of the two parents elicited highly unusual single channel gating, displaying frequent visits to two subconductance levels. The voltage dependence and kinetics of the small and large sublevels associate them with the activation of one and two subunits, respectively. The data therefore support the hypothesis that subconductance levels result from heteromeric pore conformations. In this model, both sensor movement and channel opening have a subunit basis and these processes are allosterically coupled.

Indexed as

Allosteric RegulationAnimalsCell Membrane PermeabilityDimerizationIn Vitro TechniquesIon Channel GatingKineticsMembrane PotentialsModels, BiologicalMutagenesis, Site-DirectedOocytesPatch-Clamp TechniquesProtein ConformationProtein SubunitsXenopus laevisProtein Subunits

Identifiers

PMID16043772
PMCPMC2266570

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LicenceCC BY-NC-SA
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Registered trials

None linked

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.