纳米孔
分子
序列(生物学)
DNA
共价键
材料科学
纳米技术
有机分子
化学
化学物理
有机化学
生物化学
作者
Linru Guo,Xiaolei Xing,Qiaobo Liao,Haocheng Xu,Wang Li,Xin‐Lei Ding,Xing‐Hua Xia,Li−Na Ji,Kai Xi,Kang Wang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-09-11
标识
DOI:10.1021/acsnano.4c09848
摘要
Enzyme-free single-molecule sequencing has the potential to significantly expand the application of nanopore technology to DNA, proteins, and saccharides. Despite their advantages over biological nanopores and natural suitability for enzyme-free single-molecule sequencing, conventional solid-state nanopores have not yet achieved single-molecule DNA sequencing. The biggest challenge for the accuracy of single-molecule sequencing using solid-state nanopores lies in the precise control of the pore size and conformity. In this study, we fabricated nanopore devices by covering the tip of a quartz nanopipette with ultrathin two-dimensional (2D) covalent organic framework (COF) nanosheets (pore size ≈ 1.1 nm). The size of the periodically arranged nanopores in COF is comparable to that of protein nanopores, and the structure of each COF nanopore is consistent at the atomic scale. The COF nanopore device could roughly distinguish dAMP, dCMP, dGMP, and dTMP. Furthermore, a certain percentage of the current blockades originating from 150 nucleotides model DNA molecules (13.5% for dA
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