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Rise of palmitoylation: A new trick to tune NCX1 activity.
Gök, Caglar; Fuller, William.
Afiliação
  • Gök C; School of Cardiovascular and Metabolic Health (SCMH), Sir James Black Building, University of Glasgow, Glasgow G12 8QQ, United Kingdom. Electronic address: caglar.gok@glasgow.ac.uk.
  • Fuller W; School of Cardiovascular and Metabolic Health (SCMH), Sir James Black Building, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
Biochim Biophys Acta Mol Cell Res ; 1871(5): 119719, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38574822
ABSTRACT
The cardiac Na+/Ca2+ Exchanger (NCX1) controls transmembrane calcium flux in numerous tissues. The only reversible post-translational modification established to regulate NCX1 is palmitoylation, which alters the ability of the exchanger to inactivate. Palmitoylation creates a binding site for the endogenous XIP domain, a region of the NCX1 intracellular loop established to inactivate NCX1. The binding site created by NCX1 palmitoylation sensitizes the transporter to XIP. Herein we summarize our recent knowledge on NCX1 palmitoylation and its association with cardiac pathologies, and discuss these findings in the light of the recent cryo-EM structures of human NCX1.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Processamento de Proteína Pós-Traducional / Trocador de Sódio e Cálcio / Lipoilação Limite: Animals / Humans Idioma: En Revista: Biochim Biophys Acta Mol Cell Res Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Processamento de Proteína Pós-Traducional / Trocador de Sódio e Cálcio / Lipoilação Limite: Animals / Humans Idioma: En Revista: Biochim Biophys Acta Mol Cell Res Ano de publicação: 2024 Tipo de documento: Article