| Literature DB >> 26530683 |
Fernando A Rosado-Ruiz1, Minyoung So1, Laurie S Kaguni2,3.
Abstract
The replicative mitochondrial DNA (mtDNA) helicase is essential for mtDNA replication and maintenance of the mitochondrial genome. Despite substantial advances that have been made in its characterization, there is still much to be understood about the functional roles of its domains and its interactions with the other components of the minimal mitochondrial DNA replisome. Critical to achieving this is the ability to isolate the enzyme in a stable, active form. In this chapter we describe a modified, streamlined purification strategy for recombinant forms of the enzyme. We also present assays to assess its helix unwinding activity and the stimulatory effects of the mitochondrial single-stranded DNA-binding protein (mtSSB). Finally, we describe a concentration/buffer exchange method that we have employed to achieve greater enzyme stability and appropriate conditions for biochemical and biophysical studies.Entities:
Keywords: Helicases; Human; Mitochondrial DNA replication; Mitochondrial single-stranded DNA-binding protein; mtDNA helicase
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Year: 2016 PMID: 26530683 PMCID: PMC4703107 DOI: 10.1007/978-1-4939-3040-1_14
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745