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Updated: Feb 15, 2026

Studying DNA Looping by Single-Molecule FRET
Published on: June 28, 2014
Sub-Ensemble Monitoring of DNA Strand Displacement Using Multiparameter Single-Molecule FRET
Laura E Baltierra-Jasso1, Michael J Morten1, Steven W Magennis1
1WestCHEM School of Chemistry, University of Glasgow, University Avenue, Glasgow, G12 8QQ, UK.
Abstract:
Non-enzymatic DNA strand displacement is an important mechanism in dynamic DNA nanotechnology. Here, we show that the large parameter space that is accessible by single-molecule FRET is ideal for the simultaneous monitoring of multiple reactants and products of DNA strand exchange reactions. We monitored the strand displacement from double-stranded DNA (dsDNA) by single-stranded DNA (ssDNA) at 37 °C; the data were modelled as a second-order reaction approaching equilibrium, with a rate constant of 10 m-1 s-1 . We also followed the displacement from a DNA three-way junction (3WJ) by ssDNA. The presence of three internal mismatched bases in the middle of the invading strand did not prevent displacement from the 3WJ, but reduced the second-order rate constant by about 50 %. We attribute strand exchange in the dsDNA and 3WJ to a zero-toehold pathway from the blunt-ended duplex arms. The single-molecule approach demonstrated here will be useful for studying complex DNA networks.
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