Cramer Jana, Effelsberg Daniel, Girzalsky Wolfgang, Erdmann Ralf
Department of System Biochemistry, Institute of Biochemistry and Pathobiochemistry, Medical Faculty, Ruhr-University Bochum, D-44780 Bochum, Germany.
Cold Spring Harb Protoc. 2015 Sep 1;2015(9):pdb.top074500. doi: 10.1101/pdb.top074500.
Peroxisomes are multifunctional, dynamic organelles present in nearly all eukaryotic cells. Determining their structural and functional characteristics often requires obtaining isolated and purified peroxisomes via subcellular fractionation. Subcellular fractionation techniques are generally based on a three-step procedure: preparation of a cell-free homogenate (postnuclear supernatant), generation of an organellar pellet by differential centrifugation, and density gradient centrifugation. Here we introduce methods for small-scale isolation of peroxisomes from yeast cells using different gradient media as well as large-scale purification using a two-step gradient centrifugation.
过氧化物酶体是几乎存在于所有真核细胞中的多功能动态细胞器。确定它们的结构和功能特征通常需要通过亚细胞分级分离获得分离和纯化的过氧化物酶体。亚细胞分级分离技术一般基于三步程序:制备无细胞匀浆(核后上清液)、通过差速离心产生细胞器沉淀以及密度梯度离心。在这里,我们介绍了使用不同梯度介质从酵母细胞中小规模分离过氧化物酶体的方法,以及使用两步梯度离心进行大规模纯化的方法。