Evidence map›Paper›PMID 31957808›Full record

ArticleThe Biochemical journal2020

Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the KATP channel complex.

Sean Brennan, Hussein N Rubaiy, Saba Imanzadeh, Ruth Reid, David Lodwick, Robert I Norman, Richard D Rainbow

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

7 authors at 4 institutions in 1 country.

Sean BrennanDepartment of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Sherrington Building, Ashton Street, Liverpool, Merseyside L69 3GE, U.K.
Hussein N RubaiyDepartment of Cardiovascular Sciences, University of Leicester, Clinical Sciences Wing, Glenfield General Hospital, Leicester LE3 9QP, U.K.
Saba ImanzadehDepartment of Molecular and Cell Biology, University of Leicester, Henry Wellcome Building, Lancaster Road, Leicester LE1 7RH, U.K.
Ruth ReidCentre for Biological Engineering, Loughborough University, Loughborough LE11 3TU, U.K.
David LodwickDepartment of Cardiovascular Sciences, University of Leicester, Clinical Sciences Wing, Glenfield General Hospital, Leicester LE3 9QP, U.K.
Robert I NormanLeicester Medical School, University of Leicester, George Davis Centre, Lancaster Road, Leicester LE1 7RH, U.K.
Richard D RainbowDepartment of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Sherrington Building, Ashton Street, Liverpool, Merseyside L69 3GE, U.K.
Glenfield Hospital · GBUniversity of Leicester · GBUniversity of Liverpool · GBLoughborough University · GB

Funding

British Heart Foundation PG/16/14/32039British Heart Foundation PG/19/18/34280
6 · The paper itself

Abstract

ATP-sensitive potassium (KATP) channels are widely expressed and play key roles in many tissues by coupling metabolic state to membrane excitability. The SUR subunits confer drug and enhanced nucleotide sensitivity to the pore-forming Kir6 subunit, and so information transfer between the subunits must occur. In our previous study, we identified an electrostatic interaction between Kir6 and SUR2 subunits that was key for allosteric information transfer between the regulatory and pore-forming subunit. In this study, we demonstrate a second putative interaction between Kir6.2-D323 and SUR2A-Q1336 using patch clamp electrophysiological recording, where charge swap mutation of the residues on either side of the potential interaction compromise normal channel function. The Kir6.2-D323K mutation gave rise to a constitutively active, glibenclamide and ATP-insensitive KATP complex, further confirming the importance of information transfer between the Kir6 and SUR2 subunits. Sensitivity to modulators was restored when Kir6.2-D323K was co-expressed with a reciprocal charge swap mutant, SUR-Q1336E. Importantly, equivalent interactions have been identified in both Kir6.1 and Kir6.2 suggesting this is a second important interaction between Kir6 and the proximal C terminus of SUR.

Indexed as

ATP-Binding Cassette TransportersKATP ChannelsAllosteric SiteHEK293 CellsHumansKcnj11 ChannelModels, StructuralMutationPatch-Clamp TechniquesPotassium Channels, Inwardly RectifyingSulfonylurea ReceptorsATP-Binding Cassette TransportersKATP ChannelsKcnj11 ChannelPotassium Channels, Inwardly RectifyingSulfonylurea ReceptorsABC transport proteinsKATPmolecular interactionspotassium channels

Identifiers

PMID31957808
PMCPMC7015859
OpenAlexW3000894998

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.