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Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the KATP channel complex.
Brennan, Sean; Rubaiy, Hussein N; Imanzadeh, Saba; Reid, Ruth; Lodwick, David; Norman, Robert I; Rainbow, Richard D.
Afiliação
  • Brennan S; Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Sherrington Building, Ashton Street, Liverpool, Merseyside L69 3GE, U.K.
  • Rubaiy HN; Department of Cardiovascular Sciences, University of Leicester, Clinical Sciences Wing, Glenfield General Hospital, Leicester LE3 9QP, U.K.
  • Imanzadeh S; Department of Molecular and Cell Biology, University of Leicester, Henry Wellcome Building, Lancaster Road, Leicester LE1 7RH, U.K.
  • Reid R; Centre for Biological Engineering, Loughborough University, Loughborough LE11 3TU, U.K.
  • Lodwick D; Department of Cardiovascular Sciences, University of Leicester, Clinical Sciences Wing, Glenfield General Hospital, Leicester LE3 9QP, U.K.
  • Norman RI; Leicester Medical School, University of Leicester, George Davis Centre, Lancaster Road, Leicester LE1 7RH, U.K.
  • Rainbow RD; Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Sherrington Building, Ashton Street, Liverpool, Merseyside L69 3GE, U.K.
Biochem J ; 477(3): 671-689, 2020 02 14.
Article em En | MEDLINE | ID: mdl-31957808
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transportadores de Cassetes de Ligação de ATP / Canais de Potássio Corretores do Fluxo de Internalização / Canais KATP / Receptores de Sulfonilureias Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transportadores de Cassetes de Ligação de ATP / Canais de Potássio Corretores do Fluxo de Internalização / Canais KATP / Receptores de Sulfonilureias Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article