| Literature DB >> 29087723 |
Kyle Briggs1, Gregory Madejski2, Martin Magill3, Konstantinos Kastritis3, Hendrick W de Haan3, James L McGrath2, Vincent Tabard-Cossa1.
Abstract
To reduce unwanted variation in the passage speed of DNA through solid-state nanopores, we demonstrate nanoscale preconfinement of translocating molecules using an ultrathin nanoporous silicon nitride membrane separated from a single sensing nanopore by a nanoscale cavity. We present comprehensive experimental and simulation results demonstrating that the presence of an integrated nanofilter within nanoscale distances of the sensing pore eliminates the dependence of molecular passage time distributions on pore size, revealing a global minimum in the coefficient of variation of the passage time. These results provide experimental verification that the inter- and intramolecular passage time variation depends on the conformational entropy of each molecule prior to translocation. Furthermore, we show that the observed consistently narrower passage time distributions enables a more reliable DNA length separation independent of pore size and stability. We also demonstrate that the composite nanofilter/nanopore devices can be configured to suppress the frequency of folded translocations, ensuring single-file passage of captured DNA molecules. By greatly increasing the rate at which usable data can be collected, these unique attributes will offer significant practical advantages to many solid-state nanopore-based sensing schemes, including sequencing, genomic mapping, and barcoded target detection.Entities:
Keywords: DNA; Nanopore; entropy; nanoconfinement; nanofabrication; nanotechnology
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Year: 2017 PMID: 29087723 PMCID: PMC5814347 DOI: 10.1021/acs.nanolett.7b03987
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189