HEK 293细胞
嘌呤能受体
受体
变构调节
离子通道
细胞生物学
异源表达
异源的
细胞外
膜片钳
突变
电生理学
配体门控离子通道
G蛋白偶联受体
生物
神经科学
生物物理学
信号转导
化学
生物化学
重组DNA
突变体
基因
作者
Lin‐Hua Jiang,Sébastien Roger
出处
期刊:Methods in molecular biology
日期:2019-10-24
卷期号:: 261-273
被引量:1
标识
DOI:10.1007/978-1-4939-9717-6_19
摘要
P2X receptors (P2XRs) are ligand-gated ion channels gated by extracellular adenosine 5′-triphosphate (ATP) and play a critical role in mediating ATP-induced purinergic signaling in physiological and pathological processes. Heterologous expression of P2XR in human embryonic kidney 293 (HEK293) cells and measurement of P2XR-mediated currents using patch-clamp recording technique have been widely used to study the biophysical and pharmacological properties of these receptors. Combination of electrophysiology with site-directed mutagenesis and structural information has shed light on the molecular basis for receptor activation and mechanisms of actions by receptor antagonists and modulators. It is anticipated that such methodologies will continue helping us to provide more mechanistic understanding of P2XRs and to test novel receptor antagonists and allosteric modulators for therapeutical purposes. In this chapter, we describe protocols of transiently or stably expressing the P2XR in HEK293 cells and measuring P2XR-mediated currents by using whole-cell recording.
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