Simpson Richard J
Cold Spring Harb Protoc. 2010 Jul 1;2010(7):pdb.prot5455. doi: 10.1101/pdb.prot5455.
To purify or characterize an intracellular protein, it is important to choose an efficient method for disrupting the cell or tissue that rapidly releases the protein from its intracellular compartment into a buffer that is not harmful to the biological activity of the protein of interest. One of the most widely used methods for disrupting soft tissues is homogenization. This protocol describes three processes for homogenization of animal tissues using mechanical shear: a Potter-Elvehjem glass-Teflon homogenizer, a Dounce hand homogenizer, or a handheld Waring Blendor. These methods are rapid and pose little risk to proteins other than the release of proteases from other cellular compartments. Proteolytic degradation can be minimized by the inclusion of protease inhibitors in the homogenization buffers. An optional procedure to remove mucin from tissue homogenates is also presented.
为了纯化或鉴定细胞内蛋白质,选择一种有效的方法来破坏细胞或组织很重要,这种方法能迅速将蛋白质从其细胞内区室释放到对目标蛋白质生物活性无害的缓冲液中。破坏软组织最广泛使用的方法之一是匀浆。本方案描述了使用机械剪切对动物组织进行匀浆的三种方法:波特-埃尔维耶姆玻璃-聚四氟乙烯匀浆器、邓斯手动匀浆器或手持式韦林搅拌器。这些方法速度快,除了从其他细胞区室释放蛋白酶外,对蛋白质几乎没有风险。通过在匀浆缓冲液中加入蛋白酶抑制剂,可以将蛋白水解降解降至最低。还介绍了一种从组织匀浆中去除粘蛋白的可选方法。