Li Xuhang, Donowitz Mark
GI Division, Department of Medicine, Johns Hopkins University School of Medicine, 918 Ross Research Bldg, 720 Rutland Ave, 21205, Baltimore, MD, USA,
Methods Mol Biol. 2014;1174:85-99. doi: 10.1007/978-1-4939-0944-5_6.
Density gradient ultracentrifugation (DGUC) is widely used for physical isolation (enrichment rather than purification) of subcellular membrane vesicles. It has been a valuable tool to study specific subcellular localization and dynamic trafficking of proteins. While sucrose has been the main component of density gradients, several years ago, synthetic OptiPrep™ (iodixanol) began being used for separation of organelles due to its iso-osmotic property. Here, we describe a detailed protocol for density gradient fractionation of various mammalian subcellular vesicles, including endoplasmic reticulum (ER), Golgi apparatus, endosomes, and lipid rafts, as well as apical and basolateral membranes of polarized epithelial cells.
密度梯度超速离心(DGUC)被广泛用于亚细胞膜囊泡的物理分离(富集而非纯化)。它一直是研究蛋白质特定亚细胞定位和动态运输的重要工具。虽然蔗糖一直是密度梯度的主要成分,但几年前,合成的OptiPrep™(碘克沙醇)因其等渗特性开始被用于细胞器的分离。在此,我们描述了一种详细的方案,用于对各种哺乳动物亚细胞囊泡进行密度梯度分级分离,包括内质网(ER)、高尔基体、内体和脂筏,以及极化上皮细胞的顶端和基底外侧膜。