纳米孔
化学
DNA
胸腺嘧啶
分子
胞嘧啶
共价键
碱基对
纳米技术
基础(拓扑)
碱基
结晶学
有机化学
材料科学
生物化学
数学分析
数学
作者
Xiaolei Xing,Zi-Chuan He,Saud Asif Ahmed,Qiaobo Liao,Lin-Ru Guo,Shi‐Bin Ren,Kai Xi,Li‐Na Ji,Kang Wang,Xing‐Hua Xia
标识
DOI:10.1021/acs.analchem.2c01708
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 (∼595 μs/base) compared with cytosine (∼355 μs/base) in poly(dC)6 and thymine (∼220 μs/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.
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