多巴胺转运体(DAT)功能表征的体外实验

Q2 Pharmacology, Toxicology and Pharmaceutics
Shaili Aggarwal, Ole V. Mortensen
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引用次数: 6

摘要

本单元详细介绍了研究体外摄取多巴胺(DA)作为定义多巴胺转运体功能特征的手段的方案。所有的检测都是使用市售的细胞系进行的,这些细胞系可以瞬时表达所研究的转运蛋白。提供的三种主要检测方法是:动力学检测,用于计算放射性标记的DA进入细胞的亲和力(KM)和最大速度(Vmax);浓度-响应法测定被试化合物作为运输抑制剂的效价(IC50/Ki值);以及评估配体诱导细胞内积累的DA逆向转运的能力和效力(EC50)的外排试验。虽然这些方法是使用DAT及其配体描述的,但同样的程序也可以用于研究血清素和去甲肾上腺素转运体。©2017 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In Vitro Assays for the Functional Characterization of the Dopamine Transporter (DAT)

In Vitro Assays for the Functional Characterization of the Dopamine Transporter (DAT)

In Vitro Assays for the Functional Characterization of the Dopamine Transporter (DAT)

Detailed in this unit are protocols for studying the in vitro uptake of dopamine (DA) as a means for defining the functional characteristics of dopamine transporters. All assays are performed using commercially available cell lines that transiently express the transporter under investigation. The three main assays provided are: a kinetic assay to calculate the affinity (KM) and maximal velocity (Vmax) of radiolabeled DA uptake into cells; concentration-response assays to measure the potencies (IC50/Ki values) of test compounds as transport inhibitors; and an efflux assay to assess the ability and potency (EC50) of a ligand to elicit reverse transport of DA accumulated in the cell. Although the methods are described using DAT and its ligands, the same procedure can be employed for studying serotonin and norepinephrine transporters as well. © 2017 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Pharmacology
Current Protocols in Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
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