Literature DB >> 10049691

The N-terminus of KIR6.2 limits spontaneous bursting and modulates the ATP-inhibition of KATP channels.

A P Babenko1, G Gonzalez, J Bryan.   

Abstract

KATP channels are heteromultimers of a sulfonylurea receptor SUR and KIR6.2 with the inward rectifier forming the pore which is regulated by SUR. We have examined the contributions of the cytoplasmic domains of KIR6.2 to control of spontaneous bursting and ATP-inhibition in human SUR1/KIR6.2 KATP channels. Truncations of the N-terminus of KIR6.2 nearly eliminate transitions to interburst closed states without affecting the open or intraburst closed states, thus producing SUR1/DeltaNKIR6.2 channels with an extremely high open probability in the absence of nucleotides. These channels have a decrease apparent ATP-sensitivity which is consistent with the involvement of the N-terminus in a transition to an interburst closed state that preferentially binds inhibitory ATP. Mutations in both the N- and proximal C-termini of KIR6.2 can synergistically attenuate the ATP-inhibition. The results identify the N-terminus of KIR6.2 as a determinant of the interburst kinetics of KATP channels and suggest that the two cytoplasmic domains of KIR6.2 participate in ATP-inhibitory gating through distinct mechanisms. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10049691     DOI: 10.1006/bbrc.1999.0172

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  28 in total

1.  Involvement of the n-terminus of Kir6.2 in coupling to the sulphonylurea receptor.

Authors:  F Reimann; S J Tucker; P Proks; F M Ashcroft
Journal:  J Physiol       Date:  1999-07-15       Impact factor: 5.182

2.  The I182 region of k(ir)6.2 is closely associated with ligand binding in K(ATP) channel inhibition by ATP.

Authors:  L Li; J Wang; P Drain
Journal:  Biophys J       Date:  2000-08       Impact factor: 4.033

3.  Concerted gating mechanism underlying KATP channel inhibition by ATP.

Authors:  Peter Drain; Xuehui Geng; Lehong Li
Journal:  Biophys J       Date:  2004-04       Impact factor: 4.033

4.  ATP-sensitive K+ channels: regulation of bursting by the sulphonylurea receptor, PIP2 and regions of Kir6.2.

Authors:  Bernard Ribalet; Scott A John; Lai-Hua Xie; James N Weiss
Journal:  J Physiol       Date:  2005-12-22       Impact factor: 5.182

5.  Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2-SUR1 interactions.

Authors:  Paolo Tammaro; Christophe Girard; Janne Molnes; Pål R Njølstad; Frances M Ashcroft
Journal:  EMBO J       Date:  2005-06-16       Impact factor: 11.598

6.  A mutation in the ATP-binding site of the Kir6.2 subunit of the KATP channel alters coupling with the SUR2A subunit.

Authors:  Paolo Tammaro; Frances M Ashcroft
Journal:  J Physiol       Date:  2007-09-13       Impact factor: 5.182

7.  Incomplete dissociation of glibenclamide from wild-type and mutant pancreatic K ATP channels limits their recovery from inhibition.

Authors:  U Russ; P Kühner; R Prager; D Stephan; J Bryan; U Quast
Journal:  Br J Pharmacol       Date:  2009-01-13       Impact factor: 8.739

8.  Engineered Kir6.2 mutations that correct the trafficking defect of K(ATP) channels caused by specific SUR1 mutations.

Authors:  Qing Zhou; Emily B Pratt; Show-Ling Shyng
Journal:  Channels (Austin)       Date:  2013-05-21       Impact factor: 2.581

9.  Structurally distinct ligands rescue biogenesis defects of the KATP channel complex via a converging mechanism.

Authors:  Prasanna K Devaraneni; Gregory M Martin; Erik M Olson; Qing Zhou; Show-Ling Shyng
Journal:  J Biol Chem       Date:  2015-01-30       Impact factor: 5.157

Review 10.  ABCC8 and ABCC9: ABC transporters that regulate K+ channels.

Authors:  Joseph Bryan; Alvaro Muñoz; Xinna Zhang; Martina Düfer; Gisela Drews; Peter Krippeit-Drews; Lydia Aguilar-Bryan
Journal:  Pflugers Arch       Date:  2006-08-08       Impact factor: 3.657

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