Label-Free Optical Detection of DNA Translocations through Plasmonic Nanopores

被引:116
|
作者
Verschueren, Daniel V. [1 ]
Pud, Sergii [1 ]
Shi, Xin [1 ,2 ,3 ]
De Angelis, Lorenzo [4 ]
Kuipers, L. [4 ]
Dekker, Cees [1 ]
机构
[1] Delft Univ Technol, Kavli Inst Nanosci, Dept Bionanosci, Van der Maasweg 9, NL-2629 HZ Delft, Netherlands
[2] East China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
[4] Delft Univ Technol, Kavli Inst Nanosci, Dept Quantum Nanosci, Lorentzweg 1, NL-2628 CJ Delft, Netherlands
关键词
plasmonic nanopores; plasmon resonance sensing; solid-state nanopores; DNA translocation; optical transmission; GRAPHENE NANORIBBON; CURRENT SIGNALS; SINGLE; PROTEIN; LIGHT; NANOSTRUCTURES; SCATTERING; MOLECULES; LOCATION;
D O I
10.1021/acsnano.8b06758
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid-state nanopores are single-molecule sensors that hold great potential for rapid protein and nucleic-acid analysis. Despite their many opportunities, the conventional ionic current detection scheme that is at the heart of the sensor suffers inherent limitations. This scheme intrinsically couples signal strength to the driving voltage, requires the use of high-concentration electrolytes, suffers from capacitive noise, and impairs high-density sensor integration. Here, we propose a fundamentally different detection scheme based on the enhanced light transmission through a plasmonic nanopore. We demonstrate that translocations of single DNA molecules can be optically detected, without the need of any labeling, in the transmitted light intensity through an inverted-bowtie plasmonic nanopore. Characterization and the cross-correlation of the optical signals with their electrical counterparts verify the plasmonic basis of the optical signal. We demonstrate DNA translocation event detection in a regime of driving voltages and buffer conditions where traditional ionic current sensing fails. This label-free optical detection scheme offers opportunities to probe native DNA protein interactions at physiological conditions.
引用
收藏
页码:61 / 70
页数:10
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