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A polymorphism-specific "memory" mechanism in the ß(2)-adrenergic receptor.
Ahles, Andrea; Rochais, Francesca; Frambach, Torsten; Bünemann, Moritz; Engelhardt, Stefan.
Afiliación
  • Ahles A; Institute of Pharmacology and Toxicology, Technische Universitaet Muenchen (TUM), Biedersteiner Strasse 29, 80802 Munich, Germany.
Sci Signal ; 4(185): ra53, 2011 Aug 09.
Article en En | MEDLINE | ID: mdl-21868359
Signaling through G protein (heterotrimeric guanosine triphosphate-binding protein)-coupled receptors is affected by polymorphisms in receptor-encoding genes. Using fluorescence resonance energy transfer, we found that the ß(2)-adrenergic receptor (ß(2)AR) responded to repeated activation with altered activation kinetics. Polymorphic variants of the ß(2)AR displayed divergent changes of ß(2)AR activation kinetics that closely mimicked their different efficacies to generate cyclic adenosine 3',5'-monophosphate. More efficacious variants became faster in their activation kinetics, whereas less efficacious variants became slower, compared to their initial activation. These differences depended on phosphorylation of the receptor by G protein-coupled receptor kinases. Our findings suggest an intrinsic, polymorphism-specific property of the ß(2)AR that alters activation kinetics upon continued stimulation and that may account for individual drug responses.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Transducción de Señal / Receptores Adrenérgicos beta 2 / AMP Cíclico Límite: Humans Idioma: En Revista: Sci Signal Asunto de la revista: CIENCIA / FISIOLOGIA Año: 2011 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Transducción de Señal / Receptores Adrenérgicos beta 2 / AMP Cíclico Límite: Humans Idioma: En Revista: Sci Signal Asunto de la revista: CIENCIA / FISIOLOGIA Año: 2011 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos