Strosberg A D
Laboratoire d'Immuno-Pharmacologie Moléculaire, CNRS UPR 0415, Paris, France.
Mol Neurobiol. 1990 Fall-Winter;4(3-4):211-50. doi: 10.1007/BF02780342.
The emergence of Biotechnology has provided pharmacologists with a variety of methods for investigating the structure, the function, and the regulation of membrane-bound receptors with a precision that was not imagined even five years ago. These new tools have been developed and used to analyze the known catecholamine beta 1- and beta 2-adrenergic receptors and to discover and study a new subtype, the beta 3 receptor. We review here the salient features of each of these three receptors, compare their structural and functional properties, and propose models to explain their differential regulation in time and space. A whole family of proteins has now been found to share with the beta-adrenergic receptors their most prominent features, including seven transmembrane domains and coupling with GTP-binding "G" proteins. We therefore propose that the biotechnology-based procedures developed for the beta-adrenergic receptors will be well applicable to the other members of this "R7G" family of receptors.
生物技术的出现为药理学家提供了多种方法,能够以前所未有的精准度研究膜结合受体的结构、功能和调节机制,即便在五年前这也是难以想象的。这些新工具已被开发出来,并用于分析已知的儿茶酚胺β1和β2肾上腺素能受体,以及发现和研究一种新的亚型——β3受体。在此,我们回顾这三种受体各自的显著特征,比较它们的结构和功能特性,并提出模型来解释它们在时间和空间上的差异调节。现已发现,有一整个蛋白质家族与β肾上腺素能受体具有共同的最显著特征,包括七个跨膜结构域以及与GTP结合的“G”蛋白偶联。因此,我们认为,基于生物技术开发的用于β肾上腺素能受体的程序将很好地适用于这个“R7G”受体家族的其他成员。