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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

Simulation study of the polymer translocation free energy barrier.

TL;DR: It is proposed that the theoretical models developed here can be used to make quantitatively accurate predictions of translocation free energy functions for very long polymers using simulation data acquired for short polymers.
Journal ArticleDOI

Directed motion emerging from two coupled random processes: Translocation of a chain through a membrane nanopore driven by binding proteins

TL;DR: The translocation of a stiff polymer consisting of M monomers through a nanopore in a membrane, in the presence of binding particles (chaperones) that bind onto the polymer, and partially prevent backsliding of the polymer through the pore is investigated.
Journal ArticleDOI

Polymer Translocation out of Planar Confinements

TL;DR: In this paper, the authors studied polymers in three dimensions and showed that the dwell time of polygonal polymers scales as ε(n 2 + n 2 ) for strong confinement, where the polygon is reduced to a two-dimensional polymer.
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Spontaneous translocation of a polymer across a curved membrane.

TL;DR: The objective was to establish an experimental procedure and show direct AFM measurements that unequivocally can be assigned as the limit of the proton-proton distance between the Sun and Earth.
Journal ArticleDOI

Monte Carlo simulation on polymer translocation in crowded environment.

TL;DR: The effect of crowded environment with static obstacles on the translocation of a three-dimensional self-avoiding polymer through a small pore is studied using dynamic Monte Carlo simulation, and the diffusion property of polymer chain is also influenced by obstacles.
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