Nakagawa Tatsuro, Touhara Kazushige
Biological/Pharmacological Research Laboratories, Japan Tobacco Inc., Central Pharmaceutical Research Institute, Osaka, Japan.
Methods Mol Biol. 2013;1068:107-19. doi: 10.1007/978-1-62703-619-1_8.
Reconstitution of olfactory or pheromone receptors in heterologous expression systems greatly facilitates the functional analysis of these receptors. Xenopus laevis oocytes can be used to efficiently express insect olfactory or pheromone receptors. In this chapter, we describe how to use Xenopus laevis oocytes for functional assays of insect olfactory receptors. The procedure can be subdivided into the four following steps: (1) in vitro complementary RNA (cRNA) synthesis, (2) isolation of oocytes from female Xenopus laevis, (3) cRNA microinjection into oocytes, and (4) two-electrode voltage-clamp recording. This system can be used to identify odor or pheromone ligands and to analyze structure-function relationships involving receptor proteins of interest.
在异源表达系统中重建嗅觉或信息素受体极大地促进了对这些受体的功能分析。非洲爪蟾卵母细胞可用于高效表达昆虫嗅觉或信息素受体。在本章中,我们描述了如何使用非洲爪蟾卵母细胞进行昆虫嗅觉受体的功能测定。该过程可细分为以下四个步骤:(1)体外互补RNA(cRNA)合成,(2)从非洲爪蟾雌性个体中分离卵母细胞,(3)将cRNA显微注射到卵母细胞中,以及(4)双电极电压钳记录。该系统可用于鉴定气味或信息素配体,并分析涉及感兴趣的受体蛋白的结构-功能关系。