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一种基于聚集诱导发光(AIE)分子/氧化石墨烯纳米复合材料(AIEgen@GO)的两阶段“开启”型核酸生物传感器,用于快速检测新型冠状病毒(SARS-CoV-2)病毒序列。

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

作者信息

Zhang Qin, Yin Bohan, Hao Jianhua, Ma Linjie, Huang Yingying, Shao Xueying, Li Chuanqi, Chu Zhiqin, Yi Changqing, Wong Siu Hong Dexter, Yang Mo

机构信息

Department of Biomedical Engineering The Hong Kong Polytechnic University Hong Kong China.

Department of Applied Physics The Hong Kong Polytechnic University Hong Kong China.

出版信息

Aggregate (Hoboken). 2022 Apr 11:e195. doi: 10.1002/agt2.195.

DOI:10.1002/agt2.195
PMID:35539693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9073974/
Abstract

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 ( or 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 and 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.

摘要

正在爆发的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)大流行在病毒早期诊断方面带来了重大挑战。因此,迫切需要开发一种快速、廉价且灵敏的方法来辅助即时护理SARS-CoV-2检测。在这项工作中,我们报道了一种基于纳米复合材料的高度序列特异性生物传感器,该纳米复合材料在氧化石墨烯纳米片(AIEgen@GO)上具有聚集诱导发光发光体(AIEgen)标记的寡核苷酸探针,用于一步检测SARS-CoV-2特异性核酸序列(或基因)。基于AIEgen@GO建立了一种用于病毒核酸检测的双重“开启”机制。在此,第一阶段的荧光恢复是由于在目标病毒核酸存在下AIEgen从GO表面解离,而第二阶段基于AIE的荧光信号增强是由于形成核酸双链体限制了AIEgen的分子内旋转。此外,通过检测含有ORF1ab和N基因的SARS-CoV-2病毒质粒,证明了我们平台在诊断应用中的可行性,检测时间约1小时,无需扩增,在pM水平具有良好的灵敏度。我们的平台在利用定量逆转录聚合酶链反应进行二次确认之前,在协助SARS-CoV-2核酸序列的初始快速检测方面显示出巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/79763a034687/AGT2-9999-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/51c9437bceb8/AGT2-9999-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/da1ae8af7681/AGT2-9999-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/a50b30538eeb/AGT2-9999-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/f9f30447fecf/AGT2-9999-0-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/9be27afe4f65/AGT2-9999-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/79763a034687/AGT2-9999-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/51c9437bceb8/AGT2-9999-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/da1ae8af7681/AGT2-9999-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/a50b30538eeb/AGT2-9999-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/f9f30447fecf/AGT2-9999-0-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/9be27afe4f65/AGT2-9999-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/9073974/79763a034687/AGT2-9999-0-g003.jpg

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