| Literature DB >> 28062035 |
C J Ma1, J B Steinfeld1, E C Greene2.
Abstract
Homologous recombination is an important pathway involved in the repair of double-stranded DNA breaks. Genetic studies form the foundation of our knowledge on homologous recombination. Significant progress has also been made toward understanding the biochemical and biophysical properties of the proteins, complexes, and reaction intermediates involved in this essential DNA repair pathway. However, heterogeneous or transient recombination intermediates remain extremely difficult to assess through traditional ensemble methods, leaving an incomplete mechanistic picture of many steps that take place during homologous recombination. To help overcome some of these limitations, we have established DNA curtain methodologies as an experimental platform for studying homologous DNA recombination in real-time at the single-molecule level. Here, we present a detailed overview describing the preparation and use of single-stranded DNA curtains in applications related to the study of homologous DNA recombination with emphasis on recent work related to the study of the eukaryotic recombinase Rad51.Entities:
Keywords: DNA curtains; Homologous recombination; Rad51; Total internal reflection fluorescence microscopy
Mesh:
Substances:
Year: 2016 PMID: 28062035 PMCID: PMC7229809 DOI: 10.1016/bs.mie.2016.08.005
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600