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从动物细胞中对线粒体DNA核小体进行生化分离。

Biochemical isolation of mtDNA nucleoids from animal cells.

作者信息

Bogenhagen Daniel F

机构信息

Department of Pharmacological Sciences, University at Stony Brook, Stony Brook, NY, USA.

出版信息

Methods Mol Biol. 2009;554:3-14. doi: 10.1007/978-1-59745-521-3_1.

Abstract

Mitochondrial DNA (mtDNA) in animal cells is organized into clusters of 5-7 genomes referred to as nucleoids. Contrary to the notion that mtDNA is largely free of bound proteins, these structures are nearly as rich in protein as nuclear chromatin. While the purification of intact, membrane-bound mitochondria is an established method, relatively few studies have attempted biochemical purification of mtDNA nucleoids. In this chapter, two alternative methods are presented for the purification of nucleoids. The first method yields the so-called native nucleoids, using conditions designed to preserve non-covalent protein-DNA and protein-protein interactions. The second method uses formaldehyde to crosslink proteins to mtDNA and exposes nucleoids to treatment with harsh detergents and high salt concentrations.

摘要

动物细胞中的线粒体DNA(mtDNA)被组织成5 - 7个基因组的簇,称为类核。与mtDNA基本不含结合蛋白的观点相反,这些结构中的蛋白质含量几乎与核染色质一样丰富。虽然完整的、膜结合的线粒体的纯化是一种成熟的方法,但相对较少的研究尝试对mtDNA类核进行生化纯化。在本章中,介绍了两种纯化类核的替代方法。第一种方法使用旨在保留非共价蛋白质 - DNA和蛋白质 - 蛋白质相互作用的条件,产生所谓的天然类核。第二种方法使用甲醛将蛋白质与mtDNA交联,并用苛刻的去污剂和高盐浓度处理类核。

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