Mather Michael W, Morrisey Joanne M, Vaidya Akhil B
Center for Molecular Parasitology, Department of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19129, USA.
Mol Biochem Parasitol. 2010 Dec;174(2):150-3. doi: 10.1016/j.molbiopara.2010.07.006. Epub 2010 Jul 30.
Isolation of mitochondria of high purity and with intact enzymatic activities from malaria parasites has proven to be a major obstacle in characterizing the parasite mitochondrial physiology. We describe here an improved procedure for the isolation of a mitochondrially enriched preparation from the trophozoite stage of erythrocytic Plasmodium falciparum, combining disruption by N(2) cavitation and differential centrifugation with magnetic removal of hemozoin-associated material. These mitochondrial preparations may be used to assay various mitochondrial enzyme activities, such as succinate and dihydroorotate dehydrogenases, ubiquinol-cytochrome c oxidoreductase, and cytochrome c oxidase. They also exhibit a low level of ATPase activity, which is only marginally inhibited by classical inhibitors. We have used this preparation to determine the susceptibility of mitochondrial activities to drugs and drug candidate compounds in both "wild type" and transgenic parasites.
从疟原虫中分离出具有高纯度且酶活性完整的线粒体已被证明是表征疟原虫线粒体生理学的一个主要障碍。我们在此描述一种改进的方法,用于从恶性疟原虫红细胞内期滋养体阶段分离富含线粒体的制剂,该方法将N₂空化破碎与差速离心相结合,并通过磁性去除与疟色素相关的物质。这些线粒体制剂可用于测定各种线粒体酶活性,如琥珀酸脱氢酶和二氢乳清酸脱氢酶、泛醇 - 细胞色素c氧化还原酶以及细胞色素c氧化酶。它们还表现出低水平的ATP酶活性,仅受到经典抑制剂的轻微抑制。我们已使用该制剂来确定“野生型”和转基因寄生虫中线粒体活性对药物和候选药物化合物的敏感性。