Amgen Inc., 1120 Veterans Blvd., South San Francisco, CA 94080, USA.
FEBS Lett. 2012 Apr 24;586(8):1214-9. doi: 10.1016/j.febslet.2012.03.014. Epub 2012 Mar 21.
Adhesion G-protein-coupled receptors (GPCR) are special members of GPCRs with long N-termini containing multiple domains. We overexpressed our collection of receptors together with G-proteins in mammalian cell lines and measured the concentrations of intracellular signaling molecules, such as inositol phosphate and cAMP. Our results show that a subset of tested adhesion GPCRs has constitutive activities and is capable of coupling to a variety of G-proteins. In addition, we have identified a small molecule compound that specifically activates one of the subfamily members, GPR97, and the activation was confirmed by an independent GTPγS assay. These findings suggest classical GPCR screening assays could be applied to de-orphanize these receptors, and provide pharmacological tools to improve understanding of the physiological functions of these receptors.
黏附 G 蛋白偶联受体(GPCR)是 GPCR 中的特殊成员,其 N 端较长,包含多个结构域。我们在哺乳动物细胞系中共同过表达了我们的受体集合和 G 蛋白,并测量了细胞内信号分子的浓度,如肌醇磷酸盐和 cAMP。我们的结果表明,一组测试的黏附 GPCR 具有组成型活性,并且能够与多种 G 蛋白偶联。此外,我们已经鉴定出一种小分子化合物,该化合物可特异性激活其中一个亚家族成员 GPR97,并且该激活通过独立的 GTPγS 测定得到了证实。这些发现表明,经典的 GPCR 筛选测定可应用于这些受体的去孤儿化,并提供药理学工具以改善对这些受体的生理功能的理解。