Nanopore detection of guanine derivatives based on vacancy G-quadruplex DNA

被引:0
作者
Ren, Tong [1 ]
Feng, Zhen [1 ]
Jiang, Fang [1 ]
Liu, Xingtong [1 ]
Chen, Tingting [1 ]
Guo, Yanli [1 ]
Tian, Lei [1 ]
Kang, Xiao-Feng [1 ]
Yao, Fujun [1 ]
机构
[1] Northwest Univ, Coll Chem & Mat Sci, Key Lab Synthet & Nat Funct Mol Chem, Xian 710127, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanopore; G-quadruplex; Guanine derivatives; Biosensor; Single-molecule analysis; HUMAN TELOMERE SEQUENCE; PERFORMANCE LIQUID-CHROMATOGRAPHY; SINGLE-MOLECULE ANALYSIS; STOCHASTIC DETECTION; PROTEIN; GTP; GUANOSINE; ACID; TRANSLOCATION; COMPLEXES;
D O I
10.1016/j.microc.2024.112366
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Guanine and its derivatives play fundamental roles in many biological processes and their abnormal changes are closely related to diseases. Thus, accurate and sensitive detection of them is beneficial for the early diagnosis and clinical medicine. Herein, a novel nanopore-based sensor is proposed to detection guanine and its derivatives by using a vacancy G-quadruplex (vG4) probe. In this design, the incomplete G-tetrad in vG4 probe can be filled in by guanine derivatives through Hoogsteen hydrogen bond interactions, resulting in stabilization of the Gquadruplex. Based on the different electronic signals between vG4 probe and its binding complexes, the nanopore sensor was able to achieve the detection of six guanine derivatives, including 2'-dG, Guanine, Guanosine, GMP, GDP and GTP. To demonstrate the analytical performance of the method, a guanine analogue drug was determined as model analyte. The detection limit of acyclovir was 0.0061 mu M (3 sigma/k), with a linear range of 0.01 mu M - 0.1 mu M. This sensing strategy offers a new pathway for label-free detection of nucleobases and derivatives.
引用
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页数:8
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