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Sensitive fluorescence biosensor for SARS-CoV-2 nucleocapsid protein detection in cold-chain food products based on DNA circuit and g-CNQDs@Zn-MOF.
Zhou, Chen; Lin, Chiliang; Hu, Yuyao; Zan, Haocheng; Xu, Xiaruiyan; Sun, Chengjun; Zou, Haimin; Li, Yongxin.
  • Zhou C; West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, 610041, China.
  • Lin C; West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, 610041, China.
  • Hu Y; West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, 610041, China.
  • Zan H; West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, 610041, China.
  • Xu X; West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, 610041, China.
  • Sun C; West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, 610041, China.
  • Zou H; Provincial Key Laboratory for Food Safety Monitoring and Risk Assessment of Sichuan, Chengdu, 610041, China.
  • Li Y; Department of Clinical Laboratory, Sichuan Cancer Hospital and Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610041, China.
Lebensm Wiss Technol ; 169: 114032, 2022 Nov 01.
Article in English | MEDLINE | ID: covidwho-2042006
ABSTRACT
SARS-CoV-2 isolation from cold-chain food products confirms the possibility of outbreaks through cold-chain food products. RNA extraction combined with RT-PCR is the primary method currently utilized for the detection of SARS-CoV-2. However, the requirement of hours of analytical time and the high price of RT-PCR hinder its worldwide implementation in food supervision. Here, we report a fluorescence biosensor for detection of SARS-CoV-2 N protein. The fluorescence biosensor was fabricated by aptamer-based conformational entropy-driven circuit where molecular beacon strands were labeled with graphitic carbon nitrides quantum dots@Zn-metal-organic framework (g-CNQDs@Zn-MOF) and Dabcyl. The detection of the N protein was achieved via swabbing followed by competitive assay using a fixed amount of N-48 aptamers in the analytical system. A fluorescence emission spectrum was employed for the detection. The detection limit of our fluorescence biosensor was 1.0 pg/mL for SARS-CoV-2 N protein, indicating very excellent sensitivity. The fluorescence biosensor did not exhibit significant cross-reactivity with other N proteins. Finally, the biosensor was successfully applied for the detection of SARS-CoV-2 N protein in actual cold-chain food products showing same excellent accuracy as RT-PCR method. Thus, our fluorescence biosensor is a promising analytical tool for rapid and sensitive detection of SARS-CoV-2 N protein.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Randomized controlled trials Language: English Journal: Lebensm Wiss Technol Year: 2022 Document Type: Article Affiliation country: J.lwt.2022.114032

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Randomized controlled trials Language: English Journal: Lebensm Wiss Technol Year: 2022 Document Type: Article Affiliation country: J.lwt.2022.114032