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Polymer translocation through a nanopore under an applied external field

Abstract

We investigate the dynamics of polymer translocation through a nanopore under an externally applied field using the 2D fluctuating bond model with single-segment Monte Carlo moves. We concentrate on the influence of the field strength EE, length of the chain NN, and length of the pore LL on forced translocation. As our main result, we find a crossover scaling for the translocation time τ\tau with the chain length from τN2ν\tau \sim N^{2\nu} for relatively short polymers to τN1+ν\tau \sim N^{1 + \nu} for longer chains, where ν\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 vNνv \sim N^{- \nu}, which crosses over to vN1v \sim N^{- 1} for long polymers. The reason for this is that with increasing NN 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 RR_\parallel , the radius of gyration RgR_{g} along the pore, is smaller than the pore length, we find no clear scaling of the translocation time with the chain length. For large NN, however, the asymptotic scaling τN1+ν\tau \sim N^{1 + \nu} is recovered. In this regime, τ\tau is almost independent of LL. 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 RLR_\parallel \approx L. We show here that this minimum persists for a weak fields EE such that ELEL is less than some critical value, but vanishes for large values of ELEL.Comment: 25 Pages, 10 figures. Submitted to J. Chem. Phys. J. Chem. Phys. 124, in press (2006

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