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翅成虫盘培养与弗林蛋白酶抑制剂测定

Wing Imaginal Disc Culture and Furin Inhibitor Assay.

作者信息

Sohr Alex, Du Lijuan, Roy Sougata

机构信息

Department of Cell Biology and Molecular Genetics; University of Maryland, College Park, MD 20742, USA.

出版信息

Bio Protoc. 2019 Aug 20;9(16):e3336. doi: 10.21769/BioProtoc.3336.

Abstract

Furin is an evolutionarily conserved proprotein convertase (PC) family enzyme with a broad range of substrates that are essential for developmental, homeostatic, and disease pathways. Classical genetic approaches and biochemical or cell biological assays identified that precursor forms of most growth factor family proteins are processed by Furin. To quantitatively assess the potential role of Furin in cleaving and modulating intercellular dispersion of a signaling protein, we developed a simple assay by combining genetics, organ culture, pharmacological treatment, and imaging analyses. The protocol herein describes how to culture wing imaginal discs expressing a fluorescently tagged Fibroblast Growth Factor (FGF, Branchless/Bnl) over a long period of time in the presence of Furin inhibitors and monitor the cleavage and intercellular dispersion of the truncated Bnl parts using microscopy. Although the assay described here is for assessing the effect of Furin inhibition on Bnl cleavage in the larval wing imaginal disc, the principle and methodology can easily be adopted for any other signals, tissue systems, or organisms. This strategy and protocol provide an assay for examining Furin activity on a specific substrate by directly visualizing the spatiotemporal distribution of its truncated parts in an -cultured organ.

摘要

弗林蛋白酶是一种在进化上保守的前蛋白转化酶(PC)家族酶,其底物范围广泛,对发育、稳态和疾病途径至关重要。经典遗传学方法以及生化或细胞生物学分析表明,大多数生长因子家族蛋白的前体形式是由弗林蛋白酶加工的。为了定量评估弗林蛋白酶在切割和调节信号蛋白细胞间扩散中的潜在作用,我们通过结合遗传学、器官培养、药物治疗和成像分析开发了一种简单的检测方法。本文所述方案描述了如何在存在弗林蛋白酶抑制剂的情况下,长时间培养表达荧光标记成纤维细胞生长因子(FGF,无分支/Bnl)的翅成虫盘,并使用显微镜监测截短的Bnl部分的切割和细胞间扩散。尽管此处描述的检测方法是用于评估弗林蛋白酶抑制对幼虫翅成虫盘中Bnl切割的影响,但该原理和方法可轻松应用于任何其他信号、组织系统或生物体。这种策略和方案提供了一种检测方法,通过直接观察其截短部分在离体培养器官中的时空分布来检查弗林蛋白酶对特定底物的活性。

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