利用降解fp和绿色荧光蛋白融合靶标的真核生物蛋白敲除

Q1 Biochemistry, Genetics and Molecular Biology
Emmanuel Caussinus, Oguz Kanca, Markus Affolter
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引用次数: 22

摘要

本单元描述了降解绿色荧光蛋白(降解绿色荧光蛋白),一种易于实现的蛋白敲除方法,适用于任何真核遗传系统。为了研究一种蛋白质在生物体中的功能,通常在基因水平(基因突变)或RNA水平(RNA干扰和morpholinos)上实现。然而,任何作用于蛋白质水平上游的系统都依赖于现有靶蛋白的周转率,这可能非常缓慢。相比之下,降解fp是一种直接消耗GFP融合蛋白的快速方法。特别是,降解蛋白能够在胚胎中抵消母体的影响,并导致母体贡献蛋白的早期和快速发作的功能丧失表型。咕咕叫。Protoc。蛋白质科学。73:30.2.1-30.2.13。- 2013年,John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protein Knockouts in Living Eukaryotes Using deGradFP and Green Fluorescent Protein Fusion Targets

This unit describes deGradFP (degrade Green Fluorescent Protein), an easy-to-implement protein knockout method applicable in any eukaryotic genetic system. Depleting a protein in order to study its function in a living organism is usually achieved at the gene level (genetic mutations) or at the RNA level (RNA interference and morpholinos). However, any system that acts upstream of the proteic level depends on the turnover rate of the existing target protein, which can be extremely slow. In contrast, deGradFP is a fast method that directly depletes GFP fusion proteins. In particular, deGradFP is able to counteract maternal effects in embryos and causes early and fast onset loss-of-function phenotypes of maternally contributed proteins. Curr. Protoc. Protein Sci. 73:30.2.1-30.2.13. - 2013 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Protein Science
Current Protocols in Protein Science Biochemistry, Genetics and Molecular Biology-Biochemistry
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期刊介绍: With the mapping of the human genome, more and more researchers are exploring protein structures and functions in living organisms. Current Protocols in Protein Science provides protein scientists, biochemists, molecular biologists, geneticists, and others with the first comprehensive suite of protocols for this growing field.
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