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Coexpression with potassium channel subunits used to clone the Y2 receptor for neuropeptide Y.
Rimland, J M; Seward, E P; Humbert, Y; Ratti, E; Trist, D G; North, R A.
Afiliação
  • Rimland JM; Glaxo Research Laboratories, Verona, Italy.
Mol Pharmacol ; 49(3): 387-90, 1996 Mar.
Article em En | MEDLINE | ID: mdl-8643076
ABSTRACT
Xenopus oocytes were injected with RNAs for the two inward-rectifier potassium channel subunits Kir3.1 (GIRK1) and Kir3.4 (rcKATP or CIR) in addition to RNA from the neuroblastoma cell line KAN-TS. Potassium currents were evoked by neuropeptide Y in oocytes injected with polyadenylated RNA or with cRNA from pools of a neuroblastoma (KAN-TS) cDNA library, and progressive subdivision of responding pools yielded a single cDNA. The encoded protein contains 381 amino acids, has the seven hydrophobic domains characteristic of G protein-coupled receptors, and is 31% identical to the Y1 receptor potassium currents were induced by neuropeptide Y (EC50=60pm) and Y2-selective analogues. Coexpression with potassium channel subunits will be a generally useful method for the cloning of G protein-coupled receptors.
Assuntos
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Base de dados: MEDLINE Assunto principal: Neuropeptídeo Y / Canais de Potássio / Receptores de Neuropeptídeo Y Limite: Animals / Humans Idioma: En Revista: Mol Pharmacol Ano de publicação: 1996 Tipo de documento: Article País de afiliação: Itália
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Base de dados: MEDLINE Assunto principal: Neuropeptídeo Y / Canais de Potássio / Receptores de Neuropeptídeo Y Limite: Animals / Humans Idioma: En Revista: Mol Pharmacol Ano de publicação: 1996 Tipo de documento: Article País de afiliação: Itália