Zero-length cross-linking reveals that tight interactions between the extracellular and transmembrane domains of the luteinizing hormone receptor persist during receptor activation

Molecular Endocrinology

Volumn 19, Issue 8, 2005, Pages 2086-2098

  Karges, Beate ^a   Gidenne, Stephane ^a   Aumas, Chantal ^a,b   Haddad, François ^b   Kelly, Paul A ^b   Milgrom, Edwin ^a   De Roux, Nicolas ^a,b  

^a UNIVERSITÉ PARIS SACLAY   (France)

^b INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADENYLATE CYCLASE; CHORIONIC GONADOTROPIN; CYCLIC AMP; DISULFIDE; FURIN; LUTEINIZING HORMONE; LUTEINIZING HORMONE RECEPTOR;

ARTICLE; BINDING AFFINITY; CONTROLLED STUDY; CROSS LINKING; ENZYME ACTIVITY; HORMONE ACTION; HUMAN; HUMAN CELL; MOLECULAR INTERACTION; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN INTERACTION; WESTERN BLOTTING; WILD TYPE;

ASPARTIC ACID; BINDING SITES; BLOTTING, WESTERN; CELL MEMBRANE; CELL SEPARATION; CROSS-LINKING REAGENTS; CYCLIC AMP; DISULFIDES; DOSE-RESPONSE RELATIONSHIP, DRUG; FLOW CYTOMETRY; FURIN; GLUTAMIC ACID; HUMANS; IMMUNOBLOTTING; LYSINE; MODELS, BIOLOGICAL; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; RECEPTORS, LH; RECOMBINANT PROTEINS; TIME FACTORS; TRANSFECTION;

EID: 23744497499     PISSN: 08888809     EISSN: None     Source Type: Journal    
DOI: 10.1210/me.2004-0378     Document Type: Article

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