CNIH4 interacts with newly synthesized GPCR and controls their export from the endoplasmic reticulum

Traffic

Volumn 15, Issue 4, 2014, Pages 383-400

  Sauvageau, Etienne ^a,b   Rochdi, Moulay D ^a,b,d   Oueslati, Morad ^a,b,e   Hamdan, Fadi F ^a,b,f   Percherancier, Yann ^a,b,g   Simpson, Jeremy C ^c,h   Pepperkok, Rainer ^c   Bouvier, Michel ^a,b  

^a INSTITUTE FOR RESEARCH IN IMMUNOLOGY AND CANCER   (Canada)

^b UNIVERSITÉ DE MONTRÉAL   (Canada)

^c EUROPEAN MOLECULAR BIOLOGY LABORATORY   (Germany)

^d MONTREAL HEART INSTITUTE   (Canada)

^e CATALENT PHARMA SOLUTIONS   (United States)

^f UNIVERSITY OF MONTREAL   (Canada)

^g UNIVERSITÉ BORDEAUX 1   (France)

^h UNIVERSITY COLLEGE DUBLIN   (Ireland)

Author keywords

BRET; COPII; Cornichon; Maturation; Protein protein interaction; Receptor; Trafficking

Indexed keywords

BETA 2 ADRENERGIC RECEPTOR; G PROTEIN COUPLED RECEPTOR; HUMAN CORNICHON HOMOLOGUE 4; PROTEASOME; UNCLASSIFIED DRUG; CELL RECEPTOR; CNIH4 PROTEIN, HUMAN; PROTEIN BINDING;

ARTICLE; BIOLUMINESCENCE RESONANCE ENERGY TRANSFER; CELL MATURATION; CELL SURFACE; ENDOPLASMIC RETICULUM; HUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEOMICS; SECRETORY PATHWAY; SYNTHESIS; ANIMAL; CHLOROCEBUS AETHIOPS; COS 1 CELL LINE; GENE SILENCING; GENETICS; HEK293 CELL LINE; METABOLISM; PROTEIN TRANSPORT;

ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; ENDOPLASMIC RETICULUM; GENE KNOCKDOWN TECHNIQUES; HEK293 CELLS; HUMANS; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEIN BINDING; PROTEIN TRANSPORT; RECEPTORS, CYTOPLASMIC AND NUCLEAR; RECEPTORS, G-PROTEIN-COUPLED;

EID: 84896764696     PISSN: 13989219     EISSN: 16000854     Source Type: Journal    
DOI: 10.1111/tra.12148     Document Type: Article

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