Dual acylation is required for trafficking of growth-associated protein-43 (GAP-43) to endosomal recycling compartment via an Arf6-associated endocytic vesicular pathway

Biochemical Journal

Volumn 421, Issue 3, 2009, Pages 357-369

  Trenchi, Alejandra ^a   Gomez, Guillermo A ^a   Daniotti, Jose L ^a  

^a UNIVERSIDAD NACIONAL DE CÓRDOBA   (Argentina)

Author keywords

Acylation; Golgi complex; Growth associated protein 43 (GAP 43); Membrane traffic; Palmitoyl acyl transferase; Recycling endosome

Indexed keywords

ADP-RIBOSYLATION FACTORS; BIOCHEMICAL ASSAY; CHINESE HAMSTER OVARY; CYSTEINE RESIDUES; CYTOPLASMIC LEAFLET; DOUBLE MUTATION; ENDOSOMAL RECYCLING; ENDOSOMES; GOLGI COMPLEX; GROWTH-ASSOCIATED PROTEIN-43 (GAP-43); INTRACELLULAR TRAFFICKING; LIVING CELL; MEMBRANE ASSOCIATION; NEURAL CELLS; PALMITOYL-ACYL TRANSFERASE; PERIPHERAL MEMBRANES; PHARMACOLOGICAL INHIBITION; PHOTOBLEACHING TECHNIQUES; PLASMA MEMBRANES; RECYCLING ENDOSOMES; STEADY STATE; SUBCELLULAR DISTRIBUTION; TANNIC ACID; TRANS-GOLGI NETWORK; VIDEO MICROSCOPY;

ACYLATION; ENZYMES; FLUORESCENCE MICROSCOPY; MEMBRANES; PHOTOBLEACHING; PLASMAS; RECYCLING;

CELL MEMBRANES;

ADENOSINE DIPHOSPHATE RIBOSYLATION FACTOR 6; BREFELDIN A; NEUROMODULIN; TANNIN; ADENOSINE DIPHOSPHATE RIBOSYLATION FACTOR; ADP-RIBOSYLATION FACTOR 6;

ACYLATION; ANIMAL CELL; ARTICLE; BLEACHING; CELLULAR DISTRIBUTION; CHO CELL; CONFOCAL MICROSCOPY; CONTROLLED STUDY; CYTOPLASM; ENDOCYTOSIS; ENDOSOME; FLUORESCENCE MICROSCOPY; GOLGI COMPLEX; NONHUMAN; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN LOCALIZATION; PROTEIN SYNTHESIS; PROTEIN TRANSPORT; STEADY STATE; ANIMAL; CELL MEMBRANE; CRICETULUS; GENETICS; HAMSTER; METABOLISM; MOUSE; PROTEIN BINDING; PROTEIN PROCESSING; TRANS GOLGI NETWORK; TRANSPORT VESICLE;

CRICETULUS GRISEUS;

ADP-RIBOSYLATION FACTORS; ANIMALS; CELL MEMBRANE; CHO CELLS; CRICETINAE; CRICETULUS; ENDOSOMES; GAP-43 PROTEIN; MICE; PROTEIN BINDING; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEIN TRANSPORT; TRANS-GOLGI NETWORK; TRANSPORT VESICLES;

EID: 69249248193     PISSN: 02646021     EISSN: 14708728     Source Type: Journal    
DOI: 10.1042/BJ20090484     Document Type: Article

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