A novel photosensitive dual-sensor for simultaneous detection of nucleic acids and small chemical molecules

被引:7
|
作者
Wang, Jing [1 ,2 ,3 ,4 ]
Cui, Xun [1 ,5 ]
Zhu, Jingyu [6 ,7 ,8 ,9 ]
Tan, Luxi [1 ,4 ]
Dong, Lichun [1 ,4 ]
机构
[1] Chongqing Univ, Sch Chem & Chem Engn, Chongqing 400044, Peoples R China
[2] Peking Univ, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[3] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[4] Chongqing Univ, Key Lab Low Grade Energy Utilizat Technol & Syst, Minist Educ, Chongqing 40004, Peoples R China
[5] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[6] Sichuan Univ, Sch Life Sci, Chengdu 610041, Sichuan, Peoples R China
[7] Sichuan Univ, West China Hosp, State Key Lab Biotheropy, Chengdu 610041, Sichuan, Peoples R China
[8] Sichuan Univ, West China Hosp, Canc Ctr, Chengdu 610041, Sichuan, Peoples R China
[9] Natl Collaborat Innovat Ctr, Chengdu 610041, Sichuan, Peoples R China
基金
美国国家科学基金会; 国家重点研发计划;
关键词
DNA nanotechnology; Dual-sensor; DNA melting; Gene expression; Nucleic acids; HOMOGENEOUS ELECTROCHEMICAL STRATEGY; SINGLE-CELL LEVEL; MICRORNA DETECTION; DNA; APTAMER; NANOSTRUCTURES; COCAINE; BINDING; DRUGS; PHOTOREGULATION;
D O I
10.1016/j.bios.2018.12.015
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Sensors that can rapidly and specifically detect nucleic acids and chemical molecules can revolutionize the diagnosis and treatment of diseases by allowing molecular-level informations to be used during the routine medicines. In this study, we demonstrated a novel dual-sensor that can be used to simultaneously detect any nucleic acids and chemical molecules whose binding aptamers can be found or synthesized. In the developed dual-sensor, the specifically designed PTG (a photosensitive azobenzene derivative carrying one photo" isomerizable azobenzene moiety, one threoninol terminal and one guanidinium terminal) molecules are introduced into the unwinding region of two 17 promoters, and two DNA bubbles are introduced upstream of the two T7 promoters. Without the target, the indicating gene in the dual-tensor would not be expressed since the binding with RNAPs (RNA polymerises) cannot melt the T7 promoter for the indicating gene due to the integration of the DNA double strands via the PTG molecules, manifesting the absence of the target nucleic acid and chemical molecule. While with the presence of the target nucleic acid and/or chemical molecule, the indicating gene would be expressed as the T7 promoter contained in the enlarged DNA bubble can be melted and transcribed by the bound RNAPs as the enlarged DNA bubble can help the separation of the two DNA strands, demonstrating the existence of target nucleic acid and/or chemical molecule.
引用
收藏
页码:108 / 117
页数:10
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