| Literature DB >> 31127582 |
Cody M Rogers1, Christopher W Sausen1, Matthew L Bochman2.
Abstract
Efficient replication and repair of the genome requires a multitude of protein-DNA transactions. These interactions can result in a variety of consequences for DNA such as the unwinding of double-stranded DNA (dsDNA) into single-stranded DNA (ssDNA), the annealing of complementary ssDNAs, or the exchange of ssDNA with one strand of a dsDNA duplex. Some DNA helicases possess all three activities, but many DNA-interacting proteins can also catalyze one or more of these reactions. Assays that quantify these activities are an important first step in characterizing these protein-DNA interactions in vitro. Here, we describe methods for the formation of dsDNA substrates and the assays that can be used to biochemically characterize proteins that can unwind, anneal, and/or exchange DNA strands.Keywords: DNA annealing; DNA helicase; DNA strand exchange; DNA unwinding; Radiolabeled DNA
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Year: 2019 PMID: 31127582 DOI: 10.1007/978-1-4939-9500-4_16
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745