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使用Tango系统在果蝇S2细胞中检测人类GPCR活性

Detection of Human GPCR Activity in Drosophila S2 Cells Using the Tango System.

作者信息

Salim Emil, Hori Aki, Matsubara Kohei, Takano-Shimizu Toshiyuki, Pratomo Andre Rizky, Marianne Marianne, Syahputra Armia, Husori Dadang Irfan, Inoue Asuka, Abdullah Maryam Aisyah, Shamsudin Nur Farisya, Rullah Kamal, Kuraishi Takayuki

机构信息

Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Osaka 920-1192, Japan.

Department of Pharmacology and Clinical/Community Pharmacy, Faculty of Pharmacy, Universitas Sumatera Utara, Medan 20155, Indonesia.

出版信息

Int J Mol Sci. 2024 Dec 29;26(1):202. doi: 10.3390/ijms26010202.

Abstract

G protein-coupled receptors (GPCRs) are essential cell surface proteins involved in transducing extracellular signals into intracellular responses, regulating various physiological processes. This study validated the use of the Tango assay, a sensitive method for detecting GPCR activation, in Schneider 2 (S2) cells, focusing on the human Dopamine Receptor D4 (DRD4). Plasmids encoding the LexA-tagged human DRD4 receptor and a luciferase reporter were co-transfected into S2 cells and stimulated with dopamine. Receptor activation was measured by quantifying the luciferase activity. The system showed high specificity for dopamine, with no activation in response to octopamine, a non-ligand for DRD4. Furthermore, the system effectively detects activation by a novel compound. These results demonstrate that S2 cells, coupled with the Tango assay, provide a viable model for studying human GPCR function and ligand specificity. This system enables the rapid screening of potential GPCR ligands in a cost-effective cellular model.

摘要

G蛋白偶联受体(GPCRs)是重要的细胞表面蛋白,参与将细胞外信号转化为细胞内反应,调节各种生理过程。本研究验证了Tango检测法在Schneider 2(S2)细胞中用于检测GPCR激活的有效性,该检测法是一种检测GPCR激活的灵敏方法,重点研究了人类多巴胺受体D4(DRD4)。将编码LexA标签的人类DRD4受体的质粒和荧光素酶报告基因共转染到S2细胞中,并用多巴胺刺激。通过定量荧光素酶活性来测量受体激活情况。该系统对多巴胺具有高度特异性,对章鱼胺(一种DRD4的非配体)无激活反应。此外,该系统能有效检测一种新型化合物的激活作用。这些结果表明,S2细胞与Tango检测法相结合,为研究人类GPCR功能和配体特异性提供了一个可行的模型。该系统能够在一个经济高效的细胞模型中快速筛选潜在的GPCR配体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa0/11720185/ca72adb8d0ab/ijms-26-00202-g001.jpg

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