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α1 -肾上腺素能受体亚型激活与调控的分子机制

Molecular mechanisms involved in the activation and regulation of the alpha 1-adrenergic receptor subtypes.

作者信息

Cotecchia S, Scheer A, Diviani D, Fanelli F, De Benedetti P G

机构信息

Institut de Pharmacologie et Toxicologie, Faculté de Médecine, Lausanne, Switzerland.

出版信息

Farmaco. 1998 Apr;53(4):273-7. doi: 10.1016/s0014-827x(98)00021-4.

Abstract

The adrenergic receptors (ARs) belong to the superfamily of membrane-bound G protein coupled receptors (GPCRs). Our investigation has focused on the structure-function relationship of the alpha 1b-AR subtype used as the model system for other GPCRs. Site-directed mutagenesis studies have elucidated the structural domains of the alpha 1b-AR involved in ligand binding, G protein coupling or desensitization. In addition, a combined approach using site-directed mutagenesis and molecular dynamics analysis of the alpha 1b-AR has provided information about the potential mechanisms underlying the activation process of the receptor, i.e. its transition from the 'inactive' to the 'active' conformation.

摘要

肾上腺素能受体(ARs)属于膜结合G蛋白偶联受体(GPCRs)超家族。我们的研究集中在α1b-AR亚型的结构-功能关系上,它被用作其他GPCRs的模型系统。定点突变研究阐明了α1b-AR中参与配体结合、G蛋白偶联或脱敏的结构域。此外,结合定点突变和α1b-AR分子动力学分析的方法提供了有关受体激活过程潜在机制的信息,即其从“无活性”构象转变为“活性”构象的过程。

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