File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

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

TitleAn AIEgen/graphene oxide nanocomposite (AIEgen@GO)-based two-stage “turn-on” nucleic acid biosensor for rapid detection of SARS-CoV-2 viral sequence
Authors
Keywordsaggregation-induced emission (AIE) luminogen
graphene oxide
SARS-CoV-2 detection
Issue Date2023
Citation
Aggregate, 2023, v. 4, n. 1, article no. e195 How to Cite?
AbstractThe 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.
Persistent Identifierhttp://hdl.handle.net/10722/354269
ISSN
2023 SCImago Journal Rankings: 3.994
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhang, Qin-
dc.contributor.authorYin, Bohan-
dc.contributor.authorHao, Jianhua-
dc.contributor.authorMa, Linjie-
dc.contributor.authorHuang, Yingying-
dc.contributor.authorShao, Xueying-
dc.contributor.authorLi, Chuanqi-
dc.contributor.authorChu, Zhiqin-
dc.contributor.authorYi, Changqing-
dc.contributor.authorWong, Siu Hong Dexter-
dc.contributor.authorYang, Mo-
dc.date.accessioned2025-02-07T08:47:34Z-
dc.date.available2025-02-07T08:47:34Z-
dc.date.issued2023-
dc.identifier.citationAggregate, 2023, v. 4, n. 1, article no. e195-
dc.identifier.issn2766-8541-
dc.identifier.urihttp://hdl.handle.net/10722/354269-
dc.description.abstractThe 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.-
dc.languageeng-
dc.relation.ispartofAggregate-
dc.subjectaggregation-induced emission (AIE) luminogen-
dc.subjectgraphene oxide-
dc.subjectSARS-CoV-2 detection-
dc.titleAn AIEgen/graphene oxide nanocomposite (AIEgen@GO)-based two-stage “turn-on” nucleic acid biosensor for rapid detection of SARS-CoV-2 viral sequence-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1002/agt2.195-
dc.identifier.scopuseid_2-s2.0-85153743735-
dc.identifier.volume4-
dc.identifier.issue1-
dc.identifier.spagearticle no. e195-
dc.identifier.epagearticle no. e195-
dc.identifier.eissn2692-4560-
dc.identifier.isiWOS:000780102300001-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats