Evidence map›Paper›PMID 9607935›Full record

ArticleThe Journal of general physiology1998

Kinetic structure of large-conductance Ca2+-activated K+ channels suggests that the gating includes transitions through intermediate or secondary states. A mechanism for flickers.

B S Rothberg, K L Magleby

Abstract read
In one paragraph

Article in The Journal of general physiology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Regulatory mechanisms of mitochondrial BKChannels (Austin, Tex.) · 2021
    Review
  11. Review
  12. Understanding the conformational motions of RCK gating rings.The Journal of general physiology · 2017
    Review
  13. Article
  14. Article
  15. Single-channel kinetics of BK (Slo1) channels.Frontiers in physiology · 2014
    Review
  16. Article
  17. Review
  18. Modulation of BK channel voltage gating by different auxiliary β subunits.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

B S RothbergDepartment of Physiology and Biophysics, University of Miami School of Medicine, Miami, Florida 33101-6430, USA.
K L Magleby

Funding

MECHANISMS OF IONIC CHANNEL ACTIVITYR01AR032805 · NIAMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MAGLEBY, KARL L · 1986 to 2012
$4.3M
Synapses,Channels, and Transduction in NeuroscienceT32NS007044 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MULLER, KENNETH J · 1985 to 2010
$2.2M
CHLORIDE CHANNELS IN HUMAN BRAINR01NS030584 · NINDS · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MAGLEBY, KARL L · 1993 to 1995
–
MECHANISMS OF IONIC CHANNEL ACTIVITYR37AR032805 · NIAMS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MAGLEBY, KARL L · 1988 to 1997
–
NIAMS NIH HHS AR-32805NIAMS NIH HHS R01 AR032805NINDS NIH HHS NS-007044NINDS NIH HHS NS-30584NINDS NIH HHS T32 NS007044
6 · The paper itself

Abstract

Mechanisms for the Ca2+-dependent gating of single large-conductance Ca2+-activated K+ channels from cultured rat skeletal muscle were developed using two-dimensional analysis of single-channel currents recorded with the patch clamp technique. To extract and display the essential kinetic information, the kinetic structure, from the single channel currents, adjacent open and closed intervals were binned as pairs and plotted as two-dimensional dwell-time distributions, and the excesses and deficits of the interval pairs over that expected for independent pairing were plotted as dependency plots. The basic features of the kinetic structure were generally the same among single large-conductance Ca2+-activated K+ channels, but channel-specific differences were readily apparent, suggesting heterogeneities in the gating. Simple gating schemes drawn from the Monod- Wyman-Changeux (MWC) model for allosteric proteins could approximate the basic features of the Ca2+ dependence of the kinetic structure. However, consistent differences between the observed and predicted dependency plots suggested that additional brief lifetime closed states not included in MWC-type models were involved in the gating. Adding these additional brief closed states to the MWC-type models, either beyond the activation pathway (secondary closed states) or within the activation pathway (intermediate closed states), improved the description of the Ca2+ dependence of the kinetic structure. Secondary closed states are consistent with the closing of secondary gates or channel block. Intermediate closed states are consistent with mechanisms in which the channel activates by passing through a series of intermediate conformations between the more stable open and closed states. It is the added secondary or intermediate closed states that give rise to the majority of the brief closings (flickers) in the gating.

Indexed as

AlgorithmsAnimalsCalciumCells, CulturedComputer SimulationElectric StimulationElectrophysiologyIon Channel GatingKineticsMembrane PotentialsModels, BiologicalMuscle, SkeletalPatch-Clamp TechniquesPotassium ChannelsRatsCalciumPotassium Channels

Identifiers

PMID9607935
PMCPMC2217154

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Registered trials

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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.