Cabrera Margarita, Ungermann Christian
Department of Biology, Biochemistry Section, University of Osnabrück, Osnabrück, Germany.
Methods Enzymol. 2008;451:177-96. doi: 10.1016/S0076-6879(08)03213-8.
The purification of eukaryotic organelles is a prerequisite for the detailed analysis of protein sorting, localization and translocation, membrane fusion and vesicle budding. Yeast vacuoles receive cargo from the exocytic, endocytic, and autophagic pathways and hence represent an excellent model system for the study of organelle biogenesis and protein sorting. Yeast vacuoles undergo fission and fusion in vivo, events that can be monitored in vitro by an assay that employs purified vacuoles from two tester strains. Here, we describe the methodology of yeast vacuole purification, and provide protocols for the detailed analysis of the fusion reaction. We also include methods to analyze protein dynamics on yeast vacuoles and the controls required to ensure their reliability.
真核细胞器的纯化是详细分析蛋白质分选、定位与转运、膜融合及囊泡出芽的前提条件。酵母液泡接收来自外排、内吞和自噬途径的货物,因此是研究细胞器生物发生和蛋白质分选的极佳模型系统。酵母液泡在体内会经历分裂和融合,这些过程可通过一种利用来自两个测试菌株的纯化液泡的体外测定法进行监测。在此,我们描述酵母液泡纯化的方法,并提供融合反应详细分析的方案。我们还包括分析酵母液泡上蛋白质动态的方法以及确保其可靠性所需的对照。