An AIEgen/graphene oxide nanocomposite (AIEgen@GO)-based two-stage "turn-on" nucleic acid biosensor for rapid detection of SARS-CoV-2 viral sequence

被引:44
作者
Zhang, Qin [1 ]
Yin, Bohan [1 ]
Hao, Jianhua [2 ]
Ma, Linjie [3 ]
Huang, Yingying [1 ]
Shao, Xueying [3 ]
Li, Chuanqi [1 ]
Chu, Zhiqin [3 ]
Yi, Changqing [4 ]
Wong, Siu Hong Dexter [1 ]
Yang, Mo [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Biomed Engn, Hong Kong 999077, Peoples R China
[2] Hong Kong Polytech Univ, Dept Appl Phys, Hong Kong, Peoples R China
[3] Univ Hong Kong, Joint Appointment Sch Biomed Sci, Dept Elect & Elect Engn, Hong Kong, Peoples R China
[4] Sun Yat Sen Univ, Sch Biomed Engn, Key Lab Sensing Technol & Biomed Instruments Guan, Guangzhou, Peoples R China
来源
AGGREGATE | 2023年 / 4卷 / 01期
基金
中国国家自然科学基金;
关键词
aggregation-induced emission (AIE) luminogen; graphene oxide; SARS-CoV-2; detection; AGGREGATION-INDUCED EMISSION; GRAPHENE OXIDE; HYBRIDIZATION EFFICIENCY; ULTRASENSITIVE DETECTION; FLUORESCENT-PROBE; LABEL-FREE; DNA; MOS2; FLUOROGENS; MOLECULE;
D O I
10.1002/agt2.195
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ongoing outbreak of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) pandemic has posed significant challenges in early viral diagnosis. Hence, it is urgently desirable to develop a rapid, inexpensive, and sensitive method to aid point-of-care SARS-CoV-2 detection. In this work, we report a highly sequence-specific biosensor based on nanocomposites with aggregation-induced emission luminogens (AIEgen)-labeled oligonucleotide probes on graphene oxide nanosheets (AIEgen@GO) for one step-detection of SARS-CoV-2-specific nucleic acid sequences (Orf1ab or N genes). A dual "turn-on" mechanism based on AIEgen@GO was established for viral nucleic acids detection. Here, the first-stage fluorescence recovery was due to dissociation of the AIEgen from GO surface in the presence of target viral nucleic acid, and the second-stage enhancement of AIE-based fluorescent signal was due to the formation of a nucleic acid duplex to restrict the intramolecular rotation of the AIEgen. Furthermore, the feasibility of our platform for diagnostic application was demonstrated by detecting SARS-CoV-2 virus plasmids containing both Orf1ab and N genes with rapid detection around 1 h and good sensitivity at pM level without amplification. Our platform shows great promise in assisting the initial rapid detection of the SARS-CoV-2 nucleic acid sequence before utilizing quantitative reverse transcription-polymerase chain reaction for second confirmation.
引用
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页数:12
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