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使用高内涵成像技术进行GFP-Grb2易位分析以筛选EGFR信号通路调节剂

GFP-Grb2 Translocation Assay Using High-content Imaging to Screen for Modulators of EGFR-signaling.

作者信息

Petschnigg Julia, Ketteler Robin

机构信息

MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.

出版信息

Bio Protoc. 2017 Sep 5;7(17). doi: 10.21769/BioProtoc.2528.

Abstract

High-content screening is a useful tool to understand complex cellular processes and to identify genes, proteins or small molecule compounds that modulate such pathways. High-content assays monitor the function of a protein or pathway by visualizing a change in an image-based readout, such as a change in the localization of a reporter protein. Examples of this can be the translocation of a fluorescently tagged protein from the cytoplasm to the nucleus or to the plasma membrane. One protein that is known to undergo such translocation is the Growth Factor Receptor-bound protein 2 (GRB2) that is recruited to the plasma membrane upon stimulation of a growth factor receptor and subsequently undergoes internalization. We have used GFP-tagged Grb2 previously to identify genes that are involved in EGFR signaling (Petschnigg , 2017). Ultimately, the assay can be adapted to cDNA expression cloning (Freeman ., 2012) and can be used in early stage drug discovery to identify compounds that modulate or inhibit EGFR signaling and internalization (Antczak and Djaballah, 2016).

摘要

高内涵筛选是一种了解复杂细胞过程以及识别调控此类信号通路的基因、蛋白质或小分子化合物的有用工具。高内涵分析通过可视化基于图像的读数变化(例如报告蛋白定位的变化)来监测蛋白质或信号通路的功能。此类例子可以是荧光标记蛋白从细胞质向细胞核或质膜的转位。已知会发生这种转位的一种蛋白质是生长因子受体结合蛋白2(GRB2),它在生长因子受体受到刺激时被募集到质膜,随后发生内化。我们之前已使用绿色荧光蛋白标记的Grb2来识别参与表皮生长因子受体(EGFR)信号传导的基因(佩奇尼格,2017年)。最终,该分析可适用于cDNA表达克隆(弗里曼等人,2012年),并可用于早期药物发现,以识别调节或抑制EGFR信号传导及内化的化合物(安特扎克和贾巴拉,2016年)。

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