Koenig Jennifer A
Department of Pharmacology, University of Cambridge, United Kingdom.
Methods Mol Biol. 2004;259:249-73. doi: 10.1385/1-59259-754-8:249.
Internalization of G-protein-coupled receptors (GPCRs) occurs in response to agonist activation of the receptors and causes a redistribution of receptors away from the plasma membrane toward endosomes. Internalization of lower-affinity small molecule GPCRs such as muscarinic acetylcholine and adrenergic receptors has been measured using hydrophilic antagonist radioligands that are membrane impermeant. In contrast, internalization of peptide hormone receptors is assessed by measuring the internalization of a radiolabeled- or fluorescently labeled peptide hormone. More recently, the use of epitope-tagged receptors has allowed the measurement of changes in receptor subcellular distribution by the use of immunoassay and immunofluorescence confocal microscopy. This chapter describes each of these approaches to the measurement of receptor internalization and describes the advantages and disadvantages of each method.
G蛋白偶联受体(GPCRs)的内化是受体激动剂激活的结果,会导致受体从质膜重新分布到内体。低亲和力小分子GPCRs(如毒蕈碱型乙酰胆碱受体和肾上腺素能受体)的内化已通过使用不能透过膜的亲水性拮抗剂放射性配体进行测定。相比之下,肽激素受体的内化是通过测量放射性标记或荧光标记的肽激素的内化来评估的。最近,使用表位标记受体能够通过免疫测定和免疫荧光共聚焦显微镜来测量受体内亚细胞分布的变化。本章描述了这些测量受体内化的方法,并阐述了每种方法的优缺点。