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在哺乳动物细胞和酵母中功能性表达和鉴定线虫 G 蛋白偶联受体 FLP-2(T19F4.1)

Functional expression and characterization of the C. elegans G-protein-coupled FLP-2 Receptor (T19F4.1) in mammalian cells and yeast.

机构信息

Pfizer Animal Health Discovery Research, Veterinary Medicine Discovery Research, Kalamazoo, MI 49001, USA.

Institute of Parasitology, McGill University, 21,111 Lakeshore Road, Ste-Anne de Bellevue, Quebec, Canada H9X 3V9.

出版信息

Int J Parasitol Drugs Drug Resist. 2012 Nov 15;3:1-7. doi: 10.1016/j.ijpddr.2012.10.002. eCollection 2013 Dec.

Abstract

Profound neuropeptide diversity characterizes the nematode nervous system, but it has proven challenging to match neuropeptide G protein-coupled receptors (GPCR) with their cognate ligands in heterologous systems. We have expressed the Caenorhabditis elegans GPCR encoded in the locus T19F4.1, previously matched with FMRFamide-like peptides encoded on the flp-2 precursor gene, in mammalian cells and in the yeast Saccharomyces cerevisiae. Pharmacological characterization revealed that the receptor is potently activated by flp-2 peptides in CHO cells (∼10 nM EC50) and in yeast (∼100 nM EC50), signaling through a Gqα pathway in each system. The yeast GPCR expression system provides a robust assay for screening for agonists of the flp-2 receptor and is the target of an ongoing high-throughput screening exercise.

摘要

线虫神经系统具有丰富的神经肽多样性,但在异源系统中将神经肽 G 蛋白偶联受体 (GPCR) 与其相应配体匹配一直具有挑战性。我们已经在哺乳动物细胞和酵母酿酒酵母中表达了先前与 flp-2 前体基因编码的 FMRFamide 样肽匹配的线虫 T19F4.1 基因编码的 GPCR。药理学特征表明,该受体在 CHO 细胞(约 10 nM EC50)和酵母(约 100 nM EC50)中被 flp-2 肽强烈激活,在每个系统中通过 Gqα 途径信号传导。酵母 GPCR 表达系统为筛选 flp-2 受体的激动剂提供了一种强大的测定方法,并且是正在进行的高通量筛选的目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e77b/3862401/d6af80428edc/fx1.jpg

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