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Revealing the mechanism of DNA passing through graphene and boron nitride nanopores

机译:DNA通过揭示的机制石墨烯和氮化硼纳米孔

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摘要

Nanopores on 2D materials have great potential for DNA sequencing, which is attributed to their high sequencing speed and reduced cost. However, identifying DNA bases at such a high speed with nanometer precision has remained a big challenge. Here, we implemented theoretical calculations to show the translocation of single-stranded DNA (ssDNA) through solid-state nanopores on a 2D hexagonal boron nitride (h-BN) and graphene sheet. A base-specific ssDNA sequencing technique was devised, based on the individual differences in the ion current responses for the (polyA)(16), (polyG)(16), (polyC)(16), and (polyT)(16) bases of ssDNA. Our sequential procedure for sequencing is built on a comparative approach between the current signals obtained from the nanopores to achieve base-specific detection. Our results indicate that at higher voltages (1.0, 1.2, 1.4, 1.6, 1.8 and 2.0 V nm(-1)), DNA translocation is tracked though the 1.5 and 2.0 nm nanopores, and at the 1.5 nm pore size, folded ssDNA close to the nanopore accounts for 93% and 81% of events for graphene and h-BN. Our calculations indicate charge transfer from the graphene to ssDNA, while the reverse happens in the case of the h-BN membrane. These results provide critical insights into our understanding of single molecule sequencing through solid-state nanopore research.
机译:纳米孔2 d材料有很大的潜力DNA测序,这是由于他们的高测序速度和降低成本。识别DNA碱基以如此高的速度纳米精度始终是一个巨大的挑战。在这里,我们实现了理论计算显示单链DNA的易位(ssDNA)通过二维固态纳米孔六角氮化硼(h-BN)和石墨烯床单设计,根据个体差异的离子电流响应(聚)(16),(polyG)(16)、(polyC)(16)和(polyT)(16)基地ssDNA。是建立在比较方法之间的电流信号得到的纳米孔实现base-specific检测。表明在高电压(1.0,1.2,1.4,1.6、1.8和2.0 V纳米(1)),DNA易位虽然1.5和2.0 nm纳米孔,跟踪和1.5纳米孔隙大小,折叠ssDNA接近事件的纳米孔占93%和81%石墨烯和h-BN。电荷转移从石墨烯ssDNA,h-BN发生的情况恰恰相反膜。我们对单分子的理解通过固态纳米孔测序研究。

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