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Sci Rep
2021 Nov 02;111:21539. doi: 10.1038/s41598-021-00988-y.
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Expression of truncated Kir6.2 promotes insertion of functionally inverted ATP-sensitive K+ channels.
Heitz BA
,
Bränström R
,
Yang W
,
Huang Y
,
Moede T
,
Leibiger IB
,
Leibiger B
,
Chen LQ
,
Yu J
,
Yang SN
,
Larsson O
,
Saavedra SS
,
Berggren PO
,
Aspinwall CA
.
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ATP-sensitive K+ (KATP) channels couple cellular metabolism to electrical activity in many cell types. Wild-type KATP channels are comprised of four pore forming (Kir6.x) and four regulatory (sulfonylurea receptor, SURx) subunits that each contain RKR endoplasmic reticulum retention sequences that serve to properly translocate the channel to the plasma membrane. Truncated Kir6.x variants lacking RKR sequences facilitate plasma membrane expression of functional Kir6.x in the absence of SURx; however, the effects of channel truncation on plasma membrane orientation have not been explored. To investigate the role of truncation on plasma membrane orientation of ATP sensitive K+ channels, three truncated variants of Kir6.2 were used (Kir6.2ΔC26, 6xHis-Kir6.2ΔC26, and 6xHis-EGFP-Kir6.2ΔC26). Oocyte expression of Kir6.2ΔC26 shows the presence of a population of inverted inserted channels in the plasma membrane, which is not present when co-expressed with SUR1. Immunocytochemical staining of intact and permeabilized HEK293 cells revealed that the N-terminus of 6xHis-Kir6.2ΔC26 was accessible on both sides of the plasma membrane at roughly equivalent ratios, whereas the N-terminus of 6xHis-EGFP-Kir6.2Δ26 was only accessible on the intracellular face. In HEK293 cells, whole-cell electrophysiological recordings showed a ca. 50% reduction in K+ current upon addition of ATP to the extracellular solution for 6xHis-Kir6.2ΔC26, though sensitivity to extracellular ATP was not observed in 6xHis-EGFP-Kir6.2ΔC26. Importantly, the population of channels that is inverted exhibited similar function to properly inserted channels within the plasma membrane. Taken together, these data suggest that in the absence of SURx, inverted channels can be formed from truncated Kir6.x subunits that are functionally active which may provide a new model for testing pharmacological modulators of Kir6.x, but also indicates the need for added caution when using truncated Kir6.2 mutants.
ERC-2018-AdG 834860 EYELETS European Research Council, EB007047 National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health, EB022297 National Institute of Biomedical Imaging and Bioengineering of the National Institutes of Health, 0548167 National Science Foundation, R21 EB022297 NIBIB NIH HHS , R01 EB007047 NIBIB NIH HHS
Agasid,
Expression, purification, and electrophysiological characterization of a recombinant, fluorescent Kir6.2 in mammalian cells.
2018, Pubmed
Agasid,
Expression, purification, and electrophysiological characterization of a recombinant, fluorescent Kir6.2 in mammalian cells.
2018,
Pubmed
Aguilar-Bryan,
Molecular biology of adenosine triphosphate-sensitive potassium channels.
1999,
Pubmed
Aguilar-Bryan,
Toward understanding the assembly and structure of KATP channels.
1998,
Pubmed
Alekseev,
Burst kinetics of co-expressed Kir6.2/SUR1 clones: comparison of recombinant with native ATP-sensitive K+ channel behavior.
1997,
Pubmed
Ashcroft,
Molecular defects in insulin secretion in type-2 diabetes.
2004,
Pubmed
Ashcroft,
Glucose induces closure of single potassium channels in isolated rat pancreatic beta-cells.
,
Pubmed
Ashcroft,
ATP-sensitive K+ channels: a link between B-cell metabolism and insulin secretion.
1990,
Pubmed
Ashford,
Adenosine-5'-triphosphate-sensitive ion channels in neonatal rat cultured central neurones.
1988,
Pubmed
Babenko,
Reconstituted human cardiac KATP channels: functional identity with the native channels from the sarcolemma of human ventricular cells.
1998,
Pubmed
Baukrowitz,
KATP channels gated by intracellular nucleotides and phospholipids.
2000,
Pubmed
Bokvist,
Block of ATP-regulated and Ca2(+)-activated K+ channels in mouse pancreatic beta-cells by external tetraethylammonium and quinine.
1990,
Pubmed
Bränström,
Long chain coenzyme A esters activate the pore-forming subunit (Kir6. 2) of the ATP-regulated potassium channel.
1998,
Pubmed
,
Xenbase
Clement,
Association and stoichiometry of K(ATP) channel subunits.
1997,
Pubmed
Cook,
Intracellular ATP directly blocks K+ channels in pancreatic B-cells.
,
Pubmed
Edwards,
The pharmacology of ATP-sensitive potassium channels.
1993,
Pubmed
Gasser,
Mechanism of potassium efflux and action potential shortening during ischaemia in isolated mammalian cardiac muscle.
1990,
Pubmed
Gillis,
Effects of sulfonamides on a metabolite-regulated ATPi-sensitive K+ channel in rat pancreatic B-cells.
1989,
Pubmed
Gross,
KATP channels and myocardial preconditioning: an update.
2003,
Pubmed
Haider,
Identification of the PIP2-binding site on Kir6.2 by molecular modelling and functional analysis.
2007,
Pubmed
Hilgemann,
Regulation of cardiac Na+,Ca2+ exchange and KATP potassium channels by PIP2.
1996,
Pubmed
Huopio,
K(ATP) channels and insulin secretion disorders.
2002,
Pubmed
Inagaki,
Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor.
1995,
Pubmed
Islam,
Sulfhydryl oxidation induces rapid and reversible closure of the ATP-regulated K+ channel in the pancreatic beta-cell.
1993,
Pubmed
Kuo,
Crystal structure of the potassium channel KirBac1.1 in the closed state.
2003,
Pubmed
Larsson,
Activation of the ATP-sensitive K+ channel by long chain acyl-CoA. A role in modulation of pancreatic beta-cell glucose sensitivity.
1996,
Pubmed
Larsson,
Stimulation of the KATP channel by ADP and diazoxide requires nucleotide hydrolysis in mouse pancreatic beta-cells.
1993,
Pubmed
Li,
Structure of a Pancreatic ATP-Sensitive Potassium Channel.
2017,
Pubmed
Light,
Cardiac KATP channels and ischemic preconditioning: current perspectives.
1999,
Pubmed
Mannhold,
KATP channel openers: structure-activity relationships and therapeutic potential.
2004,
Pubmed
Moreau,
SUR, ABC proteins targeted by KATP channel openers.
2005,
Pubmed
Nichols,
ATP-sensitive potassium channel modulation of the guinea pig ventricular action potential and contraction.
1991,
Pubmed
Noma,
ATP-regulated K+ channels in cardiac muscle.
,
Pubmed
Rauf,
Analysis of protein kinase A activity in insulin-secreting cells using a cell-penetrating protein substrate and capillary electrophoresis.
2010,
Pubmed
Schachter,
HEK293 human embryonic kidney cells endogenously express the P2Y1 and P2Y2 receptors.
1997,
Pubmed
Seino,
ATP-sensitive potassium channels: a model of heteromultimeric potassium channel/receptor assemblies.
1999,
Pubmed
Seino,
Physiological and pathophysiological roles of ATP-sensitive K+ channels.
2003,
Pubmed
Sharma,
The C terminus of SUR1 is required for trafficking of KATP channels.
1999,
Pubmed
Shyng,
Octameric stoichiometry of the KATP channel complex.
1997,
Pubmed
Spruce,
Voltage-dependent ATP-sensitive potassium channels of skeletal muscle membrane.
,
Pubmed
Standen,
Hyperpolarizing vasodilators activate ATP-sensitive K+ channels in arterial smooth muscle.
1989,
Pubmed
Tanabe,
Direct photoaffinity labeling of Kir6.2 by [gamma-(32)P]ATP-[gamma]4-azidoanilide.
2000,
Pubmed
,
Xenbase
Taniguchi,
Modification of the cardiac action potential by intracellular injection of adenosine triphosphate and related substances in guinea pig single ventricular cells.
1983,
Pubmed
Taschenberger,
Identification of a familial hyperinsulinism-causing mutation in the sulfonylurea receptor 1 that prevents normal trafficking and function of KATP channels.
2002,
Pubmed
Tucker,
Truncation of Kir6.2 produces ATP-sensitive K+ channels in the absence of the sulphonylurea receptor.
1997,
Pubmed
,
Xenbase
Zerangue,
A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels.
1999,
Pubmed
,
Xenbase
Zilberter,
Gating kinetics of ATP-sensitive single potassium channels in myocardial cells depends on electromotive force.
1988,
Pubmed