High Spatial Resolution of Ultrathin Covalent Organic Framework Nanopores for Single-Molecule DNA Sensing

被引:21
|
作者
Xing, Xiao-Lei [1 ]
He, Zi-Chuan [1 ]
Ahmed, Saud Asif [1 ]
Liao, Qiaobo [1 ]
Guo, Lin-Ru [1 ]
Ren, Shibin [2 ]
Xi, Kai [1 ]
Ji, Li-Na [3 ]
Wang, Kang [1 ]
Xia, Xing-Hua [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Peoples R China
[2] Taizhou Univ, Sch Pharmaceut & Mat Engn, Taizhou 317000, Peoples R China
[3] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHENE;
D O I
10.1021/acs.analchem.2c01708
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ultrathin nanosheets of two-dimensional covalent organic frameworks covered a quartz nanopipette and then acted as a nanopore device for single-molecule DNA sensing. Our results showed that a single DNA homopolymer as short as 6 bases could be detected. The dwell times of 30-mer DNA homopolymers were obviously longer than the times of 10- or 6-mer ones. For different bases, poly(dA)(6) showed the slowest transport speed (similar to 595 mu s/base) compared with cytosine (similar to 355 mu s/base) in poly(dC)(6) and thymine (similar to 220 mu s/base) in poly(dT)(6). Such translocation speeds are the slowest ever reported in two-dimensional material-based nanopores. Poly(dA)(6) also showed the biggest current blockade (94.74 pA) compared with poly(dC)(6) (79.54 pA) and poly(dT)(6) (71.41 pA). However, the present difference in blockade current was not big enough to distinguish the four DNA bases. Our study exhibits the shortest single DNA molecules that can be detected by COF nanopores at the present stage and lights the way for DNA sequencing based on solid-state nanopores.
引用
收藏
页码:9851 / 9855
页数:5
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