Hutter Harald
Department of Biological Sciences, Simon Fraser University, Burnaby, BC, Canada.
Methods Cell Biol. 2012;107:67-92. doi: 10.1016/B978-0-12-394620-1.00003-5.
Fluorescent proteins such as the "green fluorescent protein" (GFP) are popular tools in Caenorhabditis elegans, because as genetically encoded markers they are easy to introduce. Furthermore, they can be used in a living animal without the need for extensive sample preparation, because C. elegans is transparent and small enough so that entire animals can be imaged directly. Consequently, fluorescent proteins have emerged as the method of choice to study gene expression in C. elegans and reporter constructs for thousands of genes are currently available. When fused to a protein of interest, fluorescent proteins allow the imaging of its subcellular localization in vivo, offering a powerful alternative to antibody staining techniques. Fluorescent proteins can be employed to label cellular and subcellular structures and as indicators for cell physiological parameters like calcium concentration. Genetic screens relying on fluorescent proteins to visualize anatomical structures and recent progress in automation techniques have tremendously expanded their potential uses. This chapter presents tools and techniques related to the use of fluorescent proteins, discusses their advantages and shortcomings, and provides practical considerations for various applications.
荧光蛋白,如“绿色荧光蛋白”(GFP),是秀丽隐杆线虫研究中常用的工具,因为作为基因编码标记,它们易于导入。此外,由于秀丽隐杆线虫是透明的且足够小,整个动物可以直接成像,所以无需进行大量样品制备就能在活体动物中使用。因此,荧光蛋白已成为研究秀丽隐杆线虫基因表达的首选方法,目前已有数千个基因的报告构建体可供使用。当与感兴趣的蛋白质融合时,荧光蛋白能够在体内对其亚细胞定位进行成像,为抗体染色技术提供了一种强大的替代方法。荧光蛋白可用于标记细胞和亚细胞结构,并作为细胞生理参数(如钙浓度)的指标。依靠荧光蛋白来可视化解剖结构的遗传筛选以及自动化技术的最新进展极大地扩展了它们的潜在用途。本章介绍了与荧光蛋白使用相关的工具和技术,讨论了它们的优缺点,并为各种应用提供了实际考虑因素。