Motif affinity and mass spectrometry proteomic approach for the discovery of cellular AMPK targets: Identification of mitochondrial fission factor as a new AMPK substrate

Cellular Signalling

Volumn 27, Issue 5, 2015, Pages 978-988

  Ducommun, Serge ^a,b   Deak, Maria ^a   Sumpton, David ^c   Ford, Rebecca J ^d   Núñez Galindo, Antonio ^a   Kussmann, Martin ^a,b   Viollet, Benoit ^e,f,g   Steinberg, Gregory R ^d   Foretz, Marc ^e,f,g   Dayon, Loïc ^a   Morrice, Nicholas A ^c,h   Sakamoto, Kei ^a,b  

^a NESTLÉ RESEARCH CENTER   (Switzerland)

^b EPFL   (Switzerland)

^c BEATSON INSTITUTE FOR CANCER RESEARCH   (United Kingdom)

^d MCMASTER UNIVERSITY   (Canada)

^e INSTITUT COCHIN   (France)

^f CNRS   (France)

^g UNIVERSITÉ PARIS DESCARTES   (France)

^h MDS SCIEX   (Canada)

Author keywords

Cell signalling; Energy metabolism; Mitochondrial dynamics; Mitochondrial fission; Protein kinase

Indexed keywords

ADENYLATE KINASE; CELL PROTEIN; CINGULIN; IMMUNOGLOBULIN G; MITOCHONDRIAL FISSION; UNCLASSIFIED DRUG; CGN PROTEIN, MOUSE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE KINASE; MEMBRANE PROTEIN; MITOCHONDRIAL FISSION FACTOR, MOUSE; MITOCHONDRIAL PROTEIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CHROMATIN IMMUNOPRECIPITATION; CONTROLLED STUDY; ENDOTHELIUM CELL; EPITHELIUM CELL; IMMUNOPRECIPITATION; IMMUNOREACTIVITY; LIVER CELL; MALE; MASS SPECTROMETRY; MICROTUBULE; MOLECULAR WEIGHT; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN PHOSPHORYLATION; PROTEIN TARGETING; PROTEOMICS; TIGHT JUNCTION; AMINO ACID SEQUENCE; ANIMAL; C57BL MOUSE; CACO 2 CELL LINE; CELL CULTURE; HUMAN; METABOLISM; MOLECULAR GENETICS; PHOSPHORYLATION;

AMINO ACID SEQUENCE; AMP-ACTIVATED PROTEIN KINASES; ANIMALS; CACO-2 CELLS; CELLS, CULTURED; HEPATOCYTES; HUMANS; MALE; MASS SPECTROMETRY; MEMBRANE PROTEINS; MICE; MICE, INBRED C57BL; MITOCHONDRIAL PROTEINS; MOLECULAR SEQUENCE DATA; PHOSPHORYLATION; PROTEOMICS;

EID: 84925494009     PISSN: 08986568     EISSN: 18733913     Source Type: Journal    
DOI: 10.1016/j.cellsig.2015.02.008     Document Type: Article

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