Nanopore arrays in a silicon membrane for parallel single-molecule detection: DNA translocation

被引:12
作者
Zhang, Miao [1 ]
Schmidt, Torsten [1 ]
Jemt, Anders [2 ]
Sahlen, Pelin [2 ]
Sychugov, Ilya [1 ]
Lundeberg, Joakim [2 ]
Linnros, Jan [1 ]
机构
[1] KTH Royal Inst Technol, Sch Informat & Commun Technol, Mat & Nano Phys, SE-16440 Kista, Sweden
[2] KTH Royal Inst Technol, Sch Biotechnol, Sci Life Lab, SE-17165 Solna, Sweden
关键词
nanopore; parallel; single-molecule; optical; SOLID-STATE NANOPORES; FABRICATION; PROTEINS;
D O I
10.1088/0957-4484/26/31/314002
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Optical nanopore sensing offers great potential in single-molecule detection, genotyping, or DNA sequencing for high-throughput applications. However, one of the bottle-necks for fluorophore-based biomolecule sensing is the lack of an optically optimized membrane with a large array of nanopores, which has large pore-to-pore distance, small variation in pore size and low background photoluminescence (PL). Here, we demonstrate parallel detection of single-fluorophore-labeled DNA strands (450 bps) translocating through an array of silicon nanopores that fulfills the above-mentioned requirements for optical sensing. The nanopore array was fabricated using electron beam lithography and anisotropic etching followed by electrochemical etching resulting in pore diameters down to similar to 7 nm. The DNA translocation measurements were performed in a conventional wide-field microscope tailored for effective background PL control. The individual nanopore diameter was found to have a substantial effect on the translocation velocity, where smaller openings slow the translocation enough for the event to be clearly detectable in the fluorescence. Our results demonstrate that a uniform silicon nanopore array combined with wide-field optical detection is a promising alternative with which to realize massively-parallel single-molecule detection.
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收藏
页数:7
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