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酵母双杂交系统替代报告基因的评估

Evaluation of alternative reporter genes for the yeast two-hybrid system.

作者信息

Starling Alessandra L, Ortega J Miguel, Gollob Kenneth J, Vicente Elisabete J, Andrade-Nóbrega Gisele M, Rodriguez Mônica B

机构信息

Departamento de Biologia Geral, Instituto de Ciências Biologicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brasil.

出版信息

Genet Mol Res. 2003 Mar 31;2(1):124-35.

Abstract

The yeast two-hybrid system is a powerful tool for screening protein-protein interactions and has also been used for large-scale studies. We evaluated two protein-coding sequences as reporter genes for the yeast two-hybrid system, to determine if it was suitable as an alternative screening strategy. Aspergillus awamori glucoamylase activity results in clear haloes around colonies producing this enzyme after growth on starch plates and staining with iodine vapors. However, transcription activation by Gal4 on Gal-regulated promoters was insufficient for this type of phenotypic visualization. A modified gene of Aequoria victoria enhanced green fluorescent protein (EGFP) was tested to determine its suitability for interaction screenings with flow cytometry. When the EGFP reporter gene system was incorporated into the cells, Gal4 transcriptional activation produced sufficient fluorescence for detection with the flow cytometer, especially when there were strong interactions.

摘要

酵母双杂交系统是筛选蛋白质-蛋白质相互作用的强大工具,也已用于大规模研究。我们评估了两个蛋白质编码序列作为酵母双杂交系统的报告基因,以确定它是否适合作为一种替代筛选策略。泡盛曲霉葡糖淀粉酶活性会导致在淀粉平板上生长并用碘蒸气染色后,产生该酶的菌落周围出现清晰的晕圈。然而,Gal4对Gal调控启动子的转录激活不足以用于这种类型的表型可视化。对维多利亚多管水母增强型绿色荧光蛋白(EGFP)的一个修饰基因进行了测试,以确定其用于通过流式细胞术进行相互作用筛选的适用性。当将EGFP报告基因系统导入细胞时,Gal4转录激活产生了足够的荧光,可通过流式细胞仪进行检测,尤其是在存在强相互作用时。

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