ATP-sensitive potassium channels (KATP channels) couple metabolism to membrane electrical activity. In pancreatic beta-cells KATP channels alter the membrane potential in response to changes in the ATP/ADP ratio driven by glucose metabolism. To understand how KATP channels function, we cloned and reconstituted them, characterized two sets of human genes that encode their subunits, sulfonylurea receptors (SURs) and inward rectifiers (KIR6.x) respectively, and showed that mutations in SUR1 and KIR6.2 cause a recessive form of familial hyperinsulinism. The subunit functions are tightly integrated, both are required for assembly, regulation and surface expression of the heteromeric (SUR1/KIR6.2)4 channel; subunits expressed alone are retained in the ER. C-terminal truncation of KIR6.2 removes an ER retention signal allowing surface expression of a K+ channel with low sensitivity to ATP, highly modified kinetics and none of the pharmacological properties of KATP channels. Co-expression with SUR1 largely restores the native channel properties. Co-expression of SUR1 with N-terminally truncated KIR6.2 gives a channel with greatly prolonged bursts and reduced ATP sensitivity. beta-cell (SUR1) and cardiac (SUR2A) channel isoforms exhibit different kinetics and ATP sensitivity. SUR chimeras have been used to identify two regions that specify the kinetic and ATP sensitivity differences. These results begin to define a web or network of interactions that place an unidentified ATP-binding site on KIR6.2, two intracellular segments of SUR, and the N-terminus of KIR6.2 in close proximity to the mouth of the channel. Disruption of this network of interactions can affect ATP-inhibitory gating in complex ways. In this competitive renewal we propose to define the interactions within this network using peptide display, mammalian two hybrid, and epitope tagging techniques to identify the peptide segments involved. Specifically we hypothesize there are interactions between: 1) Transmembrane domain 1 (TMD1) of KIR6.2 and the TMDs of SUR, 2) the N-terminus of KIR6.2 and a segment within the first set of TMDs of SUR, 3) the C-terminus of SUR and the last 36 amino acids of KIR6.2, and 4) the last 52 amino acids of SUR and the C-terminal cytoplasmic domain of KIR6.2.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
3R01DK044311-09S1
Application #
6863099
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Blondel, Olivier
Project Start
1994-09-20
Project End
2005-02-28
Budget Start
2004-01-01
Budget End
2005-02-28
Support Year
9
Fiscal Year
2004
Total Cost
$117,739
Indirect Cost
Name
Baylor College of Medicine
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Slucca, Michela; Harmon, Jamie S; Oseid, Elizabeth A et al. (2010) ATP-sensitive K+ channel mediates the zinc switch-off signal for glucagon response during glucose deprivation. Diabetes 59:128-34
Russ, U; Kuhner, P; Prager, R et al. (2009) Incomplete dissociation of glibenclamide from wild-type and mutant pancreatic K ATP channels limits their recovery from inhibition. Br J Pharmacol 156:354-61
Winkler, Marcus; Lutz, Rebekka; Russ, Ulrich et al. (2009) Analysis of two KCNJ11 neonatal diabetes mutations, V59G and V59A, and the analogous KCNJ8 I60G substitution: differences between the channel subtypes formed with SUR1. J Biol Chem 284:6752-62
Düfer, M; Haspel, D; Krippeit-Drews, P et al. (2009) Activation of the Na+/K+-ATPase by insulin and glucose as a putative negative feedback mechanism in pancreatic beta-cells. Pflugers Arch 457:1351-60
Aguilar-Bryan, Lydia; Bryan, Joseph (2008) Neonatal diabetes mellitus. Endocr Rev 29:265-91
Dufer, Martina; Haspel, Dirk; Krippeit-Drews, Peter et al. (2007) The KATP channel is critical for calcium sequestration into non-ER compartments in mouse pancreatic beta cells. Cell Physiol Biochem 20:65-74
Bryan, Joseph; Munoz, Alvaro; Zhang, Xinna et al. (2007) ABCC8 and ABCC9: ABC transporters that regulate K+ channels. Pflugers Arch 453:703-18
Vila-Carriles, Wanda H; Zhao, Guiling; Bryan, Joseph (2007) Defining a binding pocket for sulfonylureas in ATP-sensitive potassium channels. FASEB J 21:18-25
Babenko, Andrey P; Polak, Michel; Cave, Helene et al. (2006) Activating mutations in the ABCC8 gene in neonatal diabetes mellitus. N Engl J Med 355:456-66
Babenko, Andrey P (2005) K(ATP) channels ""vingt ans apres"": ATG to PDB to Mechanism. J Mol Cell Cardiol 39:79-98

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