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游牧生物传感器:一种用于 G 蛋白偶联受体配体筛选的新型多重技术。

Nomad Biosensors: A New Multiplexed Technology for the Screening of GPCR Ligands.

机构信息

1 Innoprot (Innovative Technologies in Biological Systems), Derio, Spain.

出版信息

SLAS Technol. 2018 Jun;23(3):207-216. doi: 10.1177/2472630318754828. Epub 2018 Feb 7.

DOI:10.1177/2472630318754828
PMID:29412765
Abstract

Nomad Technology (Innoprot [Innovative Technologies in Biological Systems], Derio, Spain), a novel tool for multiplexing high-throughput cell-based G protein-coupled receptor (GPCR) assays, is described in this work. This new technology comprises a family of fluorescent biosensors called Nomad Biosensors that allow for the measurement of responses mediated by G proteins through their interactions with second-messenger transduction proteins. GPCRs are one of the largest protein families of receptors in eukaryotes, and their signaling mediates important physiological processes within cells. Thus, GPCRs are associated with a wide variety of diseases, and considered major targets in therapeutic research. Nomad constitutes a novel tool for unraveling the mechanism of GPCR signal transduction by simultaneously tracing different pathways. GPCR activation changes the structural folding of the biosensor and promotes its vesicularization, as well as an increase in the fluorescence intensity. Based on this technology, the Nomad cellular model was developed to discriminate between the Ca-mediated pathway and the cyclic adenosine monophosphate (cAMP)-mediated pathway. To validate this model, endothelin receptor B (ETR) was coexpressed into the Nomad cell line and assessed with a specific agonist, an antagonist, and a chemical library of compounds. Nomad Technology optimizes the identification of novel GPCR ligands and enables the testing of large numbers of compounds.

摘要

本文介绍了一种新型的高通量细胞 G 蛋白偶联受体(GPCR)检测的多重分析工具——游牧技术(Innoprot [创新生物系统技术],西班牙德尔里奥)。这项新技术由一系列称为游牧生物传感器的荧光生物传感器组成,可通过与第二信使转导蛋白的相互作用来测量 G 蛋白介导的反应。GPCR 是真核生物中最大的受体蛋白家族之一,其信号转导介导细胞内重要的生理过程。因此,GPCR 与多种疾病有关,被认为是治疗研究的主要靶点。游牧技术是一种新颖的工具,可通过同时追踪不同途径来揭示 GPCR 信号转导的机制。GPCR 的激活会改变生物传感器的结构折叠,并促进其囊泡化以及荧光强度的增加。基于这项技术,开发了游牧细胞模型,以区分 Ca 介导途径和环磷酸腺苷(cAMP)介导途径。为了验证该模型,将内皮素受体 B(ETR)共表达到游牧细胞系中,并使用特定激动剂、拮抗剂和化合物化学库进行评估。游牧技术优化了新型 GPCR 配体的鉴定,并能够测试大量化合物。

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