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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.
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页码:1414 / 1420
页数:7
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