Slowing down DNA Translocation through a Nanopore in Lithium Chloride

被引:346
作者
Kowalczyk, Stefan W. [1 ]
Wells, David B. [2 ,3 ]
Aksimentiev, Aleksei [2 ,3 ]
Dekker, Cees [1 ]
机构
[1] Delft Univ Technol, Kavli Inst Nanosci, NL-2628 CJ Delft, Netherlands
[2] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
[3] Univ Illinois, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Nanopore; DNA; effective charge; lithium chloride; single molecule; molecular dynamics; MOLECULAR-DYNAMICS; SINGLE; FORCE; CATIONS;
D O I
10.1021/nl204273h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The charge of a DNA molecule is a crucial parameter in many DNA detection and manipulation schemes such as gel electrophoresis and lab-on-a-chip applications. Here, we study the partial reduction of the DNA charge due to counterion binding by means of nanopore translocation experiments and all-atom molecular dynamics (MD) simulations. Surprisingly, we find that the translocation time of a DNA molecule through a solid-state nanopore strongly increases as the counterions decrease in size from K+ to Na+ to Li+, both for double-stranded DNA (dsDNA) and single-stranded DNA (ssDNA). MD simulations elucidate the microscopic origin of this effect: Li+ and Na+ bind DNA stronger than K+. These fundamental insights into the counterion binding to DNA also provide a practical method for achieving at least 10-fold enhanced resolution in nanopore applications.
引用
收藏
页码:1038 / 1044
页数:7
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