4.5 Article

Dimerization of G protein-coupled receptors: New avenues for somatostatin receptor signalling, control and functioning

期刊

MOLECULAR AND CELLULAR ENDOCRINOLOGY
卷 286, 期 1-2, 页码 63-68

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2007.12.006

关键词

dimerization; dopamine receptor; G protein-coupled receptor; opioid receptor; somatostatin receptor

向作者/读者索取更多资源

Somatostatin acts through binding and activation of five G protein-coupled receptors (GPCRs) termed somatostatin receptors or ssts (sst1-sst5). These receptors, as many other GPCRs are not just monomers but display a differential tendency to homodimerize, which varies depending on the sst subtype. Moreover, there is evidence that pairs of distinct receptors such as ssst2-sst3 and sst1-sst5 crosstalk by establishing a physical interaction, which results in altered pharmacological or/and functional properties. In addition, ssts can also heterodimerize with other families of GPCRs, as opioid and dopamine receptors, originating heterodimers which properties are different to those of their separated receptors. The present review summarizes the current knowledge on ssts homodimerization, heterodimerization, and interaction with other GPCRs, as well as how interactions affect different aspects of the normal functioning of these receptors. (C) 2007 Elsevier Ireland Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据