Journal
JOURNAL OF PHYSICAL CHEMISTRY B
Volume 118, Issue 40, Pages 11605-11612Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jp506832u
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Funding
- Biomedical Research Centre at Imperial College London
- European Research Council Starting Investigator grant
- BBSRC [BB/L017865/1] Funding Source: UKRI
- EPSRC [EP/K039946/1] Funding Source: UKRI
- Biotechnology and Biological Sciences Research Council [BB/L017865/1] Funding Source: researchfish
- Engineering and Physical Sciences Research Council [EP/K039946/1] Funding Source: researchfish
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Single-stranded DNA (ssDNA) binding protein plays an important role in the DNA replication process in a wide range of organisms. It binds to ssDNA to prevent premature reannealing and to protect it from degradation. Current understanding of SSB/ssDNA interaction points to a complex mechanism, including SSB motion along the DNA strand. We report on the first characterization of this interaction at the single-molecule level using solid-state nanopore sensors. namely without any labeling or surface immobilization. our resulsts shows that the presence of SSB on the ssDNA can control the speed of nanopore translocation, presumably due to strong interactions between SSB and the nanopore surface. This enables nanopore-based detection of ssDNA fragments as short as 37 nt, which is normally very difficult with solid state nanopore sensors, due to constraints in noise and bandwidth. Notably, tis fragment is considerably shorter than the 65 nt binding motif, typically required for SSB binding at high salt concentration. The nonspecificity of SSB binding to ssDNA further suggests that this approach could be used for fragment sizing of short ssDNA.
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