Mistry Rajendra, Dowling Mark R, Challiss R A John
Department of Cell Physiology and Pharmacology, University of Leicester, Leicester, UK.
Methods Mol Biol. 2011;746:263-75. doi: 10.1007/978-1-61779-126-0_14.
On activation, G-protein-coupled receptors (GPCRs) exert many of their cellular actions through -promoting guanine nucleotide exchange on Gα subunits of heterotrimeric G proteins to release Gα-GTP and free βγ-subunits. In membrane preparations, GTP can be substituted by ³⁵S-labeled guanosine- 5'-O-(3-thio)triphosphate ([³⁵S]GTPγS) and on agonist stimulation a quasi-stable [³⁵S]GTPγS-Gα -complex forms and accumulates. Separation of [³⁵S]GTPγS-Gα complexes from free [³⁵S]GTPγS allows differences between basal and agonist-stimulated rates of [³⁵S]GTPγS-Gα complex formation- to be used to obtain pharmacological information on receptor-G-protein information transfer. Further, by releasing Gα-subunits into solution following the [³⁵S]GTPγS binding step, Gα-subunit-specific antibodies can be used to investigate the Gα-protein subpopulations activated by receptors by immunoprecipitation of [³⁵S]GTPγS-Gα complexes and quantification by scintillation counting. Here, we describe a total [³⁵S]GTPγS binding assay and a modification of this method that incorporates a Gα-specific immunoprecipitation step.
激活后,G蛋白偶联受体(GPCRs)通过促进异源三聚体G蛋白的Gα亚基上的鸟嘌呤核苷酸交换,释放Gα-GTP和游离的βγ亚基,从而发挥许多细胞作用。在膜制剂中,GTP可被³⁵S标记的鸟苷-5'-O-(3-硫代)三磷酸([³⁵S]GTPγS)替代,在激动剂刺激下,一种准稳定的[³⁵S]GTPγS-Gα复合物形成并积累。将[³⁵S]GTPγS-Gα复合物与游离的[³⁵S]GTPγS分离,可利用基础和激动剂刺激的[³⁵S]GTPγS-Gα复合物形成速率之间的差异,来获取有关受体-G蛋白信息传递的药理学信息。此外,在[³⁵S]GTPγS结合步骤之后,通过将Gα亚基释放到溶液中,Gα亚基特异性抗体可用于通过免疫沉淀[³⁵S]GTPγS-Gα复合物并通过闪烁计数进行定量,来研究受体激活的Gα蛋白亚群。在此,我们描述了一种总[³⁵S]GTPγS结合测定法以及该方法的一种改进,该改进方法包含一个Gα特异性免疫沉淀步骤。