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A heme-binding domain controls regulation of ATP-dependent potassium channels.
Burton, Mark J; Kapetanaki, Sofia M; Chernova, Tatyana; Jamieson, Andrew G; Dorlet, Pierre; Santolini, Jérôme; Moody, Peter C E; Mitcheson, John S; Davies, Noel W; Schmid, Ralf; Raven, Emma L; Storey, Nina M.
Afiliação
  • Burton MJ; Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 9HN, United Kingdom;
  • Kapetanaki SM; Department of Chemistry, University of Leicester, Leicester LE1 7RH, United Kingdom;
  • Chernova T; MRC Toxicology Unit, Leicester LE1 9HN, United Kingdom;
  • Jamieson AG; Department of Chemistry, University of Leicester, Leicester LE1 7RH, United Kingdom;
  • Dorlet P; Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France;
  • Santolini J; Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France;
  • Moody PC; Department of Molecular and Cell Biology and Henry Wellcome Laboratories for Structural Biology, University of Leicester, Leicester LE1 9HN, United Kingdom.
  • Mitcheson JS; Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 9HN, United Kingdom;
  • Davies NW; Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 9HN, United Kingdom;
  • Schmid R; Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 9HN, United Kingdom;
  • Raven EL; Department of Chemistry, University of Leicester, Leicester LE1 7RH, United Kingdom; emma.raven@le.ac.uk ns140@le.ac.uk.
  • Storey NM; Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 9HN, United Kingdom; emma.raven@le.ac.uk ns140@le.ac.uk.
Proc Natl Acad Sci U S A ; 113(14): 3785-90, 2016 Apr 05.
Article em En | MEDLINE | ID: mdl-27006498
ABSTRACT
Heme iron has many and varied roles in biology. Most commonly it binds as a prosthetic group to proteins, and it has been widely supposed and amply demonstrated that subtle variations in the protein structure around the heme, including the heme ligands, are used to control the reactivity of the metal ion. However, the role of heme in biology now appears to also include a regulatory responsibility in the cell; this includes regulation of ion channel function. In this work, we show that cardiac KATP channels are regulated by heme. We identify a cytoplasmic heme-binding CXXHX16H motif on the sulphonylurea receptor subunit of the channel, and mutagenesis together with quantitative and spectroscopic analyses of heme-binding and single channel experiments identified Cys628 and His648 as important for heme binding. We discuss the wider implications of these findings and we use the information to present hypotheses for mechanisms of heme-dependent regulation across other ion channels.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais KATP / Receptores de Sulfonilureias / Heme Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais KATP / Receptores de Sulfonilureias / Heme Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article