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Methodological approaches for the study of GABA_A receptor pharmacology and functional responses

机译:研究GABA_A受体药理学和功能反应的方法学方法

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Inhibitory GABA_A receptor ion channels are the target for a wide range of clinically-used therapeutic agents. The complex structural diversity of these ligand-gated channels, revealed by molecular cloning studies, together with increasing requirements for higher-throughput functional assays in drug discovery, has led to the development of a wide range of techniques to examine GABA_A receptor pharmacology and function. In the current article we review some of the methodologies which have contributed to the expansion of knowledge in this field. The techniques include: molecular approaches, immunoprecipitation, and immunopurification to study receptor assembly, structure, and functional expression; in situ hybridization, immunocytochemistry, and autoradiography to examine receptor distribution in native tissues; radioligand binding, site-directed mutagenesis, and electrophysiology to examine pharmacology and allosteric modulation; and patch clamp, ion flux, microphysiometry, and a variety of novel fluorescence-based technologies to examine ion-channel function. The use of gene targetting approaches in trasgenic mice has also provided important insights into the role of specific GABA_A receptor subtypes in vivo. The continuing evolution of novel technologies and assay approaches with appropriate sensitivity and resolution to measure subtle modulation of GABA_A ion channels will facilitate ongoing investigation of the physiological functions of these important inhibitory receptors.
机译:抑制性GABA_A受体离子通道是许多临床使用的治疗剂的靶标。分子克隆研究揭示了这些配体门控通道的复杂结构多样性,以及在药物发现中对更高通量功能分析的要求不断提高,导致了检查GABA_A受体药理学和功能的多种技术的发展。在本文中,我们回顾了一些有助于扩展该领域知识的方法。这些技术包括:分子方法,免疫沉淀和免疫纯化,以研究受体的组装,结构和功能表达;原位杂交,免疫细胞化学和放射自显影以检查受体在天然组织中的分布;放射性配体结合,定点诱变和电生理检查药理学和变构调节;膜片钳,离子通量,显微生理学以及各种基于荧光的新颖技术来检查离子通道功能。基因靶向方法在转基因小鼠中的使用也为特定GABA_A受体亚型在体内的作用提供了重要见解。具有适当灵敏度和分辨率以测量GABA_A离子通道的微调的新技术和测定方法的不断发展,将有助于正在进行的这些重要抑制受体的生理功能的研究。

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