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Dynamics of polymer translocation through a nanopore under an applied external field

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TLDR
In this paper, the authors investigate the dynamics of polymer translocation through a nanopore under an externally applied field using the two-dimensional fluctuating bond model with single-segment Monte Carlo moves.
Abstract
We investigate the dynamics of polymer translocation through a nanopore under an externally applied field using the two-dimensional fluctuating bond model with single-segment Monte Carlo moves. We concentrate on the influence of the field strength E, length of the chain N, and length of the pore L on forced translocation. As our main result, we find a crossover scaling for the translocation time tau with the chain length from tau approximately N2nu for relatively short polymers to tau approximately N1+nu for longer chains, where nu is the Flory exponent. We demonstrate that this crossover is due to the change in the dependence of the translocation velocity v on the chain length. For relatively short chains v approximately N-nu, which crosses over to v approximately N(-1) for long polymers. The reason for this is that with increasing N there is a high density of segments near the exit of the pore, which slows down the translocation process due to slow relaxation of the chain. For the case of a long nanopore for which R parallel, the radius of gyration Rg along the pore, is smaller than the pore length, we find no clear scaling of the translocation time with the chain length. For large N, however, the asymptotic scaling tau approximately N1+nu is recovered. In this regime, tau is almost independent of L. We have previously found that for a polymer, which is initially placed in the middle of the pore, there is a minimum in the escape time for R parallel approximately L. We show here that this minimum persists for weak fields E such that EL is less than some critical value, but vanishes for large values of EL.

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References
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Journal ArticleDOI

Polymer translocation dynamics in the quasi-static limit.

TL;DR: This work uses a multiple-histogram method and the Fokker-Planck formalism to calculate the variation of the free energy with Q, a coordinate used to quantify the degree of translocation in a quasi-static regime of polymer-nanopore friction.
Journal ArticleDOI

Effect of charge patterns along a solid-state nanopore on polyelectrolyte translocation

TL;DR: A theory based on the Fokker-Planck formalism is found to successfully describe the observed trends with reasonable quantitative agreement, and longest average translocation time is observed for a pattern corresponding to an optimum section length.
Journal ArticleDOI

Kinetics and mechanism of plasmid DNA penetration through nanopores

TL;DR: It is shown that double-stranded plasmid DNA with a 350 nm hydrodynamic diameter penetrates through membrane pores as narrow as 10 nm under pressure, and suggested that the supercoiled plasmids penetrate through these narrow pores by stretching into long hair-shaped flexible strands.
Journal ArticleDOI

Simulations of two-dimensional unbiased polymer translocation using the bond fluctuation model

TL;DR: It is shown that for the BFM if the simulations are extended to longer polymers, the purported scaling tau(d) approximately N(1+2nu) ceases to hold, and that BFM simulations do not rule out the theoretical prediction for unbiased translocation, namely, beta=2+nu.
Journal ArticleDOI

Polymer translocation under time-dependent driving forces: resonant activation induced by attractive polymer-pore interactions.

TL;DR: It is found that the nature of the interaction fundamentally affects the translocation dynamics of polymers under time-dependent driving forces, and that the attractive pore case can be a minimum at the optimal frequency of the force, the so-called resonant activation.
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