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

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 surface...

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Main Authors: Xixi Song (Author), Ying Tao (Author), Sumin Bian (Author), Mohamad Sawan (Author)
Format: Book
Published: Elsevier, 2024-10-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Xixi Song  |e author 
700 1 0 |a Ying Tao  |e author 
700 1 0 |a Sumin Bian  |e author 
700 1 0 |a Mohamad Sawan  |e author 
245 0 0 |a Optical biosensing of monkeypox virus using novel recombinant silica-binding proteins for site-directed antibody immobilization 
260 |b Elsevier,   |c 2024-10-01T00:00:00Z. 
500 |a 2095-1779 
500 |a 10.1016/j.jpha.2024.100995 
520 |a 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 (2C2) 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 (SA)-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. 
546 |a EN 
690 |a Site-directed immobilization 
690 |a Silica-binding proteins 
690 |a Optical biosensing 
690 |a Monkeypox virus 
690 |a Spiked clinical samples 
690 |a Multi-virus biosensor 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmaceutical Analysis, Vol 14, Iss 10, Pp 100995- (2024) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2095177924000923 
787 0 |n https://doaj.org/toc/2095-1779 
856 4 1 |u https://doaj.org/article/0e2267d4b8aa4540a6d3c0f2d3ee9b28  |z Connect to this object online.