Kovalchuk Andriy, Weber Stefan S, Nijland Jeroen G, Bovenberg Roel A L, Driessen Arnold J M
Faculty of Agriculture and Forestry, Department of Forest Sciences, Forest Pathology, University of Helsinki, Helsinki, Finland.
Methods Mol Biol. 2012;835:1-16. doi: 10.1007/978-1-61779-501-5_1.
Fungal cells are highly complex as their metabolism is compartmentalized harboring various types of subcellular organelles that are bordered by one or more membranes. Knowledge about the intracellular localization of transporter proteins is often required for the understanding of their biological function. Among different approaches available, the localization analysis based on the expression of GFP fusions is commonly used as a relatively fast and cost-efficient method that allows visualization of proteins of interest in both live and fixed cells. In addition, inactivation of transporter genes is an important tool to resolve their specific function. Here we provide a detailed protocol for the deletion and localization analysis of ABC transporters in the filamentous fungus Penicillium chrysogenum. It includes construction of expression plasmids, their transformation into fungal strains, cultivation of transformants, microscopy analysis, as well as additional protocols on staining of fungal cells with organelle-specific dyes like Hoechst 33342, MitoTracker DeepRed, and FM4-64.
真菌细胞高度复杂,因为其新陈代谢是分区化的,含有各种类型的亚细胞器,这些亚细胞器由一层或多层膜包围。为了理解转运蛋白的生物学功能,通常需要了解其细胞内定位。在现有的不同方法中,基于绿色荧光蛋白(GFP)融合表达的定位分析是一种常用的相对快速且经济高效的方法,它能够在活细胞和固定细胞中观察到感兴趣的蛋白质。此外,转运蛋白基因的失活是解析其特定功能的重要工具。在此,我们提供了一份详细的方案,用于丝状真菌产黄青霉中ABC转运蛋白的缺失和定位分析。该方案包括表达质粒的构建、将其转化到真菌菌株中、转化体的培养、显微镜分析,以及使用诸如Hoechst 33342、MitoTracker DeepRed和FM4 - 64等细胞器特异性染料对真菌细胞进行染色的其他方案。