On the distribution of DNA translocation times in solid-state nanopores: an analysis using Schrödinger's first-passage-time theory.
On the distribution of DNA translocation times in solid-state nanopores: an analysis using Schrödinger's first-passage-time theory.
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DOI:
10.1088/0953-8984/25/37/375102
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发表时间:
2013-09-18
期刊:
影响因子:
--
通讯作者:
Ling XS
中科院分区:
文献类型:
--
作者:
Ling DY;Ling XS
In this short note, a correction is made to the recently proposed solution to a 1D biased diffusion model for linear DNA translocation and a new analysis will be given to the data in. It was pointed out by us recently that this 1D linear translocation model is equivalent to the one that was considered by Schrödinger for the Enrenhaft-Millikan measurements on electron charge. Here we apply Schrödinger’s first-passage-time distribution formula to the data set in. It is found that Schrödinger’s formula can be used to describe the time distribution of DNA translocation in solid-state nanopores. These fittings yield two useful parameters: drift velocity of DNA translocation and diffusion constant of DNA inside the nanopore. The results suggest two regimes of DNA translocation: (I) at low voltages, there are clear deviations from Smoluchowski’s linear law of electrophoresis which we attribute to the entropic barrier effects; (II) at high voltages, the translocation velocity is a linear function of the applied electric field. In regime II, the apparent diffusion constant exhibits a quadratic dependence on applied electric field, suggesting a mechanism of Taylor dispersion effect likely due the electro-osmotic flow field in the nanopore channel. This analysis yields a dispersion-free diffusion constant value of 11.2 nm2/µs for the segment of DNA inside the nanopore which is in agreement with Stokes-Einstein theory quantitatively. The implication of Schrödinger’s formula for DNA sequencing is discussed.