Protein-free, ultrasensitive miRNA analysis based on an entropy-driven catalytic reaction switched on a smart-responsive DNAzyme dual-walker amplification strategy

被引:9
|
作者
Fan, Zhichao [1 ,2 ]
Zhao, Xiang [2 ]
Dong, Yan [2 ]
Zhou, Jie [3 ]
Li, Yingxue [1 ]
Wang, Junyi [2 ]
Qi, Yuchen [1 ,2 ]
Tan, Congcong [1 ,2 ]
Yu, Hua [1 ,4 ]
Li, Jianjun [2 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Med & Life Sci, Chengdu 611137, Peoples R China
[2] Third Mil Med Univ, Army Med Univ, Southwest Hosp, Dept Oncol, Chongqing 400038, Peoples R China
[3] Xingcheng Special Serv Sanat Strateg Support Force, Dept Lab Med, Huludao 125100, Peoples R China
[4] Hosp Chengdu Univ Tradit Chinese Med, Dept Gen Surg, Chengdu 610072, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA walker; DNAzyme; Entropy-driven catalytic reaction; miRNA analysis; LIVING CELLS; MICRORNA;
D O I
10.1016/j.ijbiomac.2022.11.084
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs), useful biomarkers for cancer diagnosis, play an important role in tumorigenesis and progression, but many of the current analysis methods can suffer from excessive protease dependence, being time-consuming and unsatisfactory performance. Therefore, a reliable sensing strategy for the protein-free, ul-trasensitive analysis of tumor-associated miRNAs is desired. The proposed dual-walker biosensing strategy based on an entropy-driven catalytic (EDC) walker coupled with a smart-responsive DNAzyme walker was demon-strated for the dual-amplification detection of miRNA-21. Namely, the target miRNA-21 initiates the three-stranded substrate complex of the traditional EDC circuit to release the input trigger of the Dz walker, which recognizes the circular binding domain to restore the cleavage activity of the DzS-AuNP walker. The fluorescence signal continuously released from the AuNPs was recorded by a fluorescence reader for miRNA-21 sensing. The optimized dual-walker exhibited appreciable sensitivity with a detection limit of 70 fM, satisfactory flexibility, fine specificity and ideal stability for clinical serum sample assays. The proposed strategy may open a new avenue for the development of powerful DNA molecular tools for cancer diagnosis.
引用
收藏
页码:931 / 938
页数:8
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