Xiao Jiping, Bergson Clare
Cardiovascular Institute, University of Pennsylvania, Philadelphia, PA, USA.
Methods Mol Biol. 2013;964:3-13. doi: 10.1007/978-1-62703-251-3_1.
Dopamine receptors are a class of metabotropic G protein-coupled receptors. Plasma membrane expression is a key determinant of receptor signaling, and one that is regulated both by extra and intracellular cues. Abnormal dopamine receptor signaling is implicated in several neuropsychiatric disorders, including schizophrenia and attention deficit hyperactivity disorder, as well as drug abuse. Here, we describe in detail the application of two complementary applications of protein biotinylation and enzyme-linked immunoabsorbent assay (ELISA) for detecting and quantifying levels of dopamine receptors expressed on the cell surface. In the biotinylation method, cell surface receptors are labeled with Sulfo-NHS-biotin. The charge on the sulfonyl facilitates water solubility of the reactive biotin compound and prevents its diffusion across the plasma membrane. In the ELISA method, surface labeling is achieved with antibodies specific to extracellular epitopes on the receptors, and by fixing the cells without detergent such that the plasma membrane remains intact.
多巴胺受体是一类代谢型G蛋白偶联受体。质膜表达是受体信号传导的关键决定因素,并且受到细胞外和细胞内信号的共同调节。多巴胺受体信号异常与多种神经精神疾病有关,包括精神分裂症和注意力缺陷多动障碍,以及药物滥用。在此,我们详细描述了蛋白质生物素化和酶联免疫吸附测定(ELISA)这两种互补方法在检测和定量细胞表面表达的多巴胺受体水平方面的应用。在生物素化方法中,细胞表面受体用磺基-NHS-生物素标记。磺酰基上的电荷促进了反应性生物素化合物的水溶性,并防止其扩散穿过质膜。在ELISA方法中,通过针对受体细胞外表位的特异性抗体进行表面标记,并在不使用去污剂的情况下固定细胞,以使质膜保持完整。