State Key Laboratory of Microbial Metabolism & Joint International Research Laboratory of Metabolic & Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University.
State Key Laboratory of Microbial Metabolism & Joint International Research Laboratory of Metabolic & Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University;
J Vis Exp. 2022 Apr 20(182). doi: 10.3791/63846.
The budding yeast, Saccharomyces cerevisiae, is a classic model system in studying organelle function and dynamics. In our previous works, we have constructed fluorescent protein-based markers for major organelles and endomembrane structures, including the nucleus, endoplasmic reticulum (ER), Golgi apparatus, endosomes, vacuoles, mitochondria, peroxisomes, lipid droplets, and autophagosomes. The protocol presented here describes the procedures for using these markers in yeast, including DNA preparation for yeast transformation, selection and evaluation of transformants, fluorescent microscopic observation, and the expected outcomes. The text is geared toward researchers who are entering the field of yeast organelle study from other backgrounds. Essential steps are covered, as well as technical notes about microscope hardware considerations and several common pitfalls. It provides a starting point for people to observe yeast subcellular entities by live-cell fluorescent microscopy. These tools and methods can be used to identify protein subcellular localization and track organelles of interest in time-lapse imaging.
budding yeast,Saccharomyces cerevisiae,是研究细胞器功能和动态的经典模式生物系统。在我们之前的工作中,我们构建了基于荧光蛋白的主要细胞器和内膜结构的标记物,包括细胞核、内质网(ER)、高尔基体、内体、液泡、线粒体、过氧化物酶体、脂滴和自噬体。本方案介绍了在酵母中使用这些标记物的步骤,包括酵母转化的 DNA 制备、转化子的选择和评估、荧光显微镜观察以及预期结果。本文面向的是从其他背景进入酵母细胞器研究领域的研究人员。涵盖了基本步骤,并提供了有关显微镜硬件考虑因素和几个常见陷阱的技术说明。它为人们通过活细胞荧光显微镜观察酵母亚细胞实体提供了一个起点。这些工具和方法可用于确定蛋白质的亚细胞定位,并在延时成像中跟踪感兴趣的细胞器。