Nanoconfined circular and linear DNA - equilibrium conformations and unfolding kinetics
arXiv:1605.00886 · doi:10.1021/ma5022067
Abstract
Studies of circular DNA confined to nanofluidic channels are relevant both from a fundamental polymer-physics perspective and due to the importance of circular DNA molecules in vivo. We here observe the unfolding of DNA from the circular to linear configuration as a light-induced double strand break occurs, characterize the dynamics, and compare the equilibrium conformational statistics of linear and circular configurations. This is important because it allows us to determine to which extent existing statistical theories describe the extension of confined circular DNA. We find that the ratio of the extensions of confined linear and circular DNA configurations increases as the buffer concentration decreases. The experimental results fall between theoretical predictions for the extended de Gennes regime at weaker confinement and the Odijk regime at stronger confinement. We show that it is possible to directly distinguish between circular and linear DNA molecules by measuring the emission intensity from the DNA. Finally, we determine the rate of unfolding and show that this rate is larger for more confined DNA, possibly reflecting the corresponding larger difference in entropy between the circular and linear configurations.
21 pages, 7 figures, 1 table
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- One-parameter scaling theory for DNA extension in a nanochannel
- Extension of nano-confined DNA: quantitative comparison between experiment and theory
- Free energy of a folded polymer under cylindrical confinement
- Free energy of a folded semiflexible polymer confined to a nanochannel of various geometries
- Stochastic unfolding of nanoconfined DNA: experiments, model and Bayesian analysis
- Distribution of label spacings for genome mapping in nanochannels
- Hairpins in the conformations of a confined polymer
- Stability of sedimenting flexible loops