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Xixi Song, Ying Tao, Sumin Bian, Mohamad Sawan. Optical biosensing of monkeypox virus using novel recombinant silica-binding proteins for site-directed antibody immobilization[J]. Journal of Pharmaceutical Analysis. doi: 10.1016/j.jpha.2024.100995
Citation: Xixi Song, Ying Tao, Sumin Bian, Mohamad Sawan. Optical biosensing of monkeypox virus using novel recombinant silica-binding proteins for site-directed antibody immobilization[J]. Journal of Pharmaceutical Analysis. doi: 10.1016/j.jpha.2024.100995

Optical biosensing of monkeypox virus using novel recombinant silica-binding proteins for site-directed antibody immobilization

doi: 10.1016/j.jpha.2024.100995
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This research was supported by Westlake University, China (Startup funds), the Research Center for Industries of the Future of Westlake University, China (Grant No.: WU2022C040), and the National Natural Science Foundation of China (Grant No.: 82104122).

  • Received Date: Jan. 30, 2024
  • Accepted Date: Apr. 29, 2024
  • Rev Recd Date: Apr. 26, 2024
  • Available Online: May 10, 2024
  • The efficient immobilization of capture antibodies is crucial for timely pathogen detection during global pandemic outbreaks. Therefore, we proposed a silica-binding protein featuring core functional domains (cSP). It comprises a peptide with a silica-binding tag designed to adhere to silica surfaces and tandem protein G fragments for effective antibody capture. This innovation facilitates precise site-directed immobilization of antibodies onto silica surfaces. We applied cSP to silica-coated optical fibers, creating a fiber-optic biolayer interferometer (FO-BLI) biosensor capable of monitoring the Monkeypox Virus (MPXV) Protein A29L in spiked clinical samples to rapidly detect the MPXV. The cSP-based FO-BLI biosensor for MPXV demonstrated a limit of detection (LOD) of 0.62 ng/mL in buffer, comparable to the 0.52 ng/mL LOD achieved using a conventional streptavidin-based FO-BLI biosensor. Furthermore, it achieved LODs of 0.77 ng/mL in spiked serum and 0.80 ng/mL in spiked saliva, exhibiting no cross-reactivity with other viral antigens. The MPXV detection process was completed within 14 min. We further proposed a cSP-based multi-virus biosensor strategy capable of detecting various pandemic strains, such as MPXV, the latest coronavirus disease (COVID) variants, and influenza A protein, to extend its versatility. The proposed cSP-modified FO-BLI biosensor has a high potential for rapidly and accurately detecting MPXV antigens, making valuable contributions to epidemiological studies.
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