Signal amplification strategy of DNA self-assembled biosensor and typical applications in pathogenic microorganism detection

被引:2
|
作者
Bai, Yuxin [1 ]
Xu, Pingyao [2 ]
Li, Shi [2 ]
Wang, Dongsheng [2 ]
Zhang, Kaijiong [2 ]
Zheng, Dongming [1 ]
Yue, Daifan [1 ]
Zhang, Guiji [2 ]
He, Shuya [2 ]
Li, Yan [1 ]
Zou, Haimin [2 ]
Deng, Yao [2 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Coll Med Technol, Chengdu 610075, Peoples R China
[2] Univ Elect Sci & Technol China, Affiliated Canc Hosp, Sichuan Canc Ctr, Sichuan Canc Hosp & Inst,Sichuan Clin Res Ctr Canc, Chengdu 610041, Peoples R China
关键词
DNA self-assembly; Catalytic hairpin assembly; Hybridization chain reaction; Nanomaterials; Pathogenic microorganism detection; HYBRIDIZATION CHAIN-REACTION; ULTRASENSITIVE DETECTION; HAIRPIN; FLUORESCENCE; MICRORNA; PROBES;
D O I
10.1016/j.talanta.2024.125759
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Biosensors have emerged as ideal analytical devices for various bio-applications owing to their low cost, convenience, and portability, which offer great potential for improving global healthcare. DNA self-assembly techniques have been enriched with the development of innovative amplification strategies, such as dispersion-to-localization of catalytic hairpin assembly, and dumbbell hybridization chain reaction, which hold great significance for building biosensors capable of realizing sensitive, rapid and multiplexed detection of pathogenic microorganisms. Here, focusing primarily on the signal amplification strategies based on DNA selfassembly, we concisely summarized the strengths and weaknesses of diverse isothermal nucleic acid amplification techniques. Subsequently, both single-layer and cascade amplification strategies based on traditional catalytic hairpin assembly and hybridization chain reaction were critically explored. Furthermore, a comprehensive overview of the recent advances in DNA self-assembled biosensors for the detection of pathogenic microorganisms is presented to summarize methods for biorecognition and signal amplification. Finally, a brief discussion is provided about the current challenges and future directions of DNA self-assembled biosensors.
引用
收藏
页数:16
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