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A bivalent form of a RBD-specific synthetic antibody effectively neutralizes SARS-CoV-2 variants

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Authors

Kim, Dong-Gun; Kim, Uijin; Park, In Ho; Ryu, Bumhan; Yoo, Youngki; Cha, Jeong Seok; Yoon, Ga-Yeon; Kim, Sung-Hee; Oh, Heeju; Seo, Jun-Young; Nam, Ki Taek; Seong, Je Kyug; Shin, Jeon-Soo; Cho, Hyun-Soo; Kim, Hak-Sung

Issue Date
2023-12
Publisher
Elsevier BV
Citation
Antiviral Research, Vol.220, p. 105738
Abstract
Coronavirus Disease 2019 (COVID-19) pandemic is severely impacting the world, and tremendous efforts have been made to deal with it. Despite many advances in vaccines and therapeutics, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants remains an intractable challenge. We present a bivalent Receptor Binding Domain (RBD)-specific synthetic antibody, specific for the RBD of wild-type (lineage A), developed from a non-antibody protein scaffold composed of LRR (Leucine-rich repeat) modules through phage display. We further reinforced the unique feature of the synthetic antibody by constructing a tandem dimeric form. The resulting bivalent form showed a broader neutralizing activity against the variants. The in vivo neutralizing efficacy of the bivalent synthetic antibody was confirmed using a human ACE2-expressing mouse model that significantly alleviated viral titer and lung infection. The present approach can be used to develop a synthetic antibody showing a broader neutralizing activity against a multitude of SARS-CoV-2 variants.
ISSN
0166-3542
URI
https://hdl.handle.net/10371/204965
DOI
https://doi.org/10.1016/j.antiviral.2023.105738
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