Evidence map›Paper›PMID 26490875›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

A Critical Gating Switch at a Modulatory Site in Neuronal Kir3 Channels.

Scott K Adney, Junghoon Ha, Xuan-Yu Meng, Takeharu Kawano, Diomedes E Logothetis

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.6field-weighted citation impact, top 30% of its field
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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. PKC isoform-specific targeting of the phosphorylation site SerinePflugers Archiv : European journal of physiology · 2026
    Article
  2. Angiotensin receptors and αPflugers Archiv : European journal of physiology · 2024
    Article
  3. Article
  4. Mechanism of PKCε regulation of cardiac GIRK channel gating.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Article
  7. Neuronal G protein-gated KAmerican journal of physiology. Cell physiology · 2022
    Review
  8. PKC regulation of ion channels: The involvement of PIPThe Journal of biological chemistry · 2022
    Review
  9. Roles of PLCβ, PIPJournal of cellular physiology · 2022
    Article
  10. Article
  11. Article
  12. Activation of VNeuropharmacology · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Dynamic role of the tether helix in PIPThe Journal of general physiology · 2017
    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

5 authors at 1 institution in 1 country.

Scott K AdneyDepartment of Physiology and Biophysics, School of Medicine, Virginia Commonwealth University, Richmond, Virginia 23298.
Junghoon HaDepartment of Physiology and Biophysics, School of Medicine, Virginia Commonwealth University, Richmond, Virginia 23298.
Xuan-Yu MengDepartment of Physiology and Biophysics, School of Medicine, Virginia Commonwealth University, Richmond, Virginia 23298.
Takeharu KawanoDepartment of Physiology and Biophysics, School of Medicine, Virginia Commonwealth University, Richmond, Virginia 23298.
Diomedes E LogothetisDepartment of Physiology and Biophysics, School of Medicine, Virginia Commonwealth University, Richmond, Virginia 23298 delogothetis@vcu.edu.ORCID http://orcid.org/0000-0002-0384-073X
Virginia Commonwealth University · US

Funding

Structural Determinants of PIP2 RegulationR01HL059949 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Leigh Daniel Plant · 1998 to 2026
$11.6M
Modulation of Kir Channel Function by PhosphorylationR01HL090882 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI LOGOTHETIS, DIOMEDES E. · 2009 to 2012
$1.5M
NHLBI NIH HHS R01 HL059949NHLBI NIH HHS R01 HL090882NHLBI NIH HHS R01HL090882NHLBI NIH HHS R01HL59949
6 · The paper itself

Abstract

Inwardly rectifying potassium channels enforce tight control of resting membrane potential in excitable cells. The Kir3.2 channel, a member of the Kir3 subfamily of G-protein-activated potassium channels (GIRKs), plays several roles in the nervous system, including key responsibility in the GABAB pathway of inhibition, in pain perception pathways via opioid receptors, and is also involved in alcoholism. PKC phosphorylation acts on the channel to reduce activity, yet the mechanism is incompletely understood. Using the heterologous Xenopus oocyte system combined with molecular dynamics simulations, we show that PKC modulation of channel activity is dependent on Ser-196 in Kir3.2 such that, when this site is phosphorylated, the channel is less sensitive to PKC inhibition. This reduced inhibition is dependent on an interaction between phospho-Ser (SEP)-196 and Arg-201, reducing Arg-201 interaction with the sodium-binding site Asp-228. Neutralization of either SEP-196 or Arg-201 leads to a channel with reduced activity and increased sensitivity to PKC inhibition. This study clarifies the role of Ser-196 as an allosteric modulator of PKC inhibition and suggests that the SEP-196/Arg-201 interaction is critical for maintaining maximal channel activity. SIGNIFICANCE STATEMENT: The inwardly rectifying potassium 3.2 (Kir3.2) channel is found principally in neurons that regulate diverse brain functions, including pain perception, alcoholism, and substance addiction. Activation or inhibition of this channel leads to changes in neuronal firing and chemical message transmission. The Kir3.2 channel is subject to regulation by intracellular signals including sodium, G-proteins, ethanol, the phospholipid phosphatidylinositol bis-phosphate, and phosphorylation by protein kinases. Here, we take advantage of the recently published structure of Kir3.2 to provide an in-depth molecular view of how phosphorylation of a specific residue previously thought to be the target of PKC promotes channel gating and acts as an allosteric modulator of PKC-mediated inhibition.

Indexed as

AnimalsBiophysical PhenomenaElectric StimulationEnzyme InhibitorsFemaleG Protein-Coupled Inwardly-Rectifying Potassium ChannelsGreen Fluorescent ProteinsIon Channel GatingMembrane PotentialsMicroinjectionsModels, MolecularOocytesPatch-Clamp TechniquesPhorbol 12,13-DibutyratePhosphatidylinositol 4,5-DiphosphatePhosphorylationEnzyme InhibitorsG Protein-Coupled Inwardly-Rectifying Potassium ChannelsGreen Fluorescent ProteinsPhorbol 12,13-DibutyratePhosphatidylinositol 4,5-DiphosphateProtein Kinase CSerineGIRKKir3PIP2PKC

Identifiers

PMID26490875
PMCPMC4683693
OpenAlexW2346346950

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.