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Discrimination of the H1N1 and H5N2 Variants of Influenza A Virus Using an Isomeric Sialic Acid-Conjugated Graphene Field-Effect Transistor.
Nazir, Sophia; Kim, Kyung Ho; Kim, Lina; Seo, Sung Eun; Bae, Pan Kee; An, Jai Eun; Kwon, Oh Seok.
  • Nazir S; Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.
  • Kim KH; Department of Biotechnology, University of Science and Technology (UST), 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.
  • Kim L; Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.
  • Seo SE; Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.
  • Bae PK; Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.
  • An JE; BioNano Health Guard Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.
  • Kwon OS; Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, Republic of Korea.
Anal Chem ; 95(13): 5532-5541, 2023 04 04.
Article in English | MEDLINE | ID: covidwho-2300795
ABSTRACT
There has been a continuous effort to fabricate a fast, sensitive, and inexpensive system for influenza virus detection to meet the demand for effective screening in point-of-care testing. Herein, we report a sialic acid (SA)-conjugated graphene field-effect transistor (SA-GFET) sensor designed using α2,3-linked sialic acid (3'-SA) and α2,6-linked sialic acid (6'-SA) for the detection and discrimination of the hemagglutinin (HA) protein of the H5N2 and H1N1 viruses. 3'-SA and 6'-SA specific for H5 and H1 influenza were used in the SA-GFET to capture the HA protein of the influenza virus. The net charge of the captured viral sample led to a change in the electrical current of the SA-GFET platform, which could be correlated to the concentration of the viral sample. This SA-GFET platform exhibited a highly sensitive response in the range of 101-106 pfu mL-1, with a limit of detection (LOD) of 101 pfu mL-1 in buffer solution and a response time of approximately 10 s. The selectivity of the SA-GFET platform for the H1N1 and H5N2 influenza viruses was verified by testing analogous respiratory viruses, i.e., influenza B and the spike protein of SARS-CoV-2 and MERS-CoV, on the SA-GFET. Overall, the results demonstrate that the developed dual-channel SA-GFET platform can potentially serve as a highly efficient and sensitive sensing platform for the rapid detection of infectious diseases.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Influenza A virus / Influenza, Human / Influenza A Virus, H1N1 Subtype / Influenza A Virus, H5N2 Subtype / COVID-19 / Graphite Type of study: Diagnostic study / Experimental Studies Topics: Variants Limits: Humans Language: English Journal: Anal Chem Year: 2023 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Influenza A virus / Influenza, Human / Influenza A Virus, H1N1 Subtype / Influenza A Virus, H5N2 Subtype / COVID-19 / Graphite Type of study: Diagnostic study / Experimental Studies Topics: Variants Limits: Humans Language: English Journal: Anal Chem Year: 2023 Document Type: Article