Unraveling Single-Stranded DNA in a Solid-State Nanopore

被引:102
作者
Kowalczyk, Stefan W. [1 ]
Tuijtel, Maarten W. [1 ]
Donkers, Serge P. [1 ]
Dekker, Cees [1 ]
机构
[1] Delft Univ Technol, Kavli Inst Nanosci, NL-2628 CJ Delft, Netherlands
关键词
Nanopores; translocation; single-stranded DNA; sequencing; POLYNUCLEOTIDE MOLECULES; DISCRIMINATION; FORCE; ACID; MECHANICS; NM;
D O I
10.1021/nl100271c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid-state nanopores are an emerging class of single-molecule sensors. Whereas most studies so far focused on double-stranded DNA (dsDNA) molecules, exploration of single-stranded DNA (ssDNA) is of great interest as well, for example to employ such a nanopore device to read out the sequence. Here, we study the translocation of long random-sequence ssDNA through nanopores. Using atomic force microscopy, we observe the ssDNA to hybridize into a random coil, forming blobs of around 100 am in diameter For 7 kb ssDNA. These large entangled structures have to unravel, when they arrive at the pore entrance. Indeed, we observe strong blockade events with a translocation time that is exponentially dependent on voltage, tau similar to e-(VIV0). Interestingly, this is very different than for dsDNA, for which tau similar to 1/V. We report translocations of ssDNA but also of ssDNA dsDNA constructs where we compare the conductance-blockade levels for ssDNA versus dsDNA as a function of voltage.
引用
收藏
页码:1414 / 1420
页数:7
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