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Antibody-like proteins that capture and neutralize SARS-CoV-2.
Kondo, T; Iwatani, Y; Matsuoka, K; Fujino, T; Umemoto, S; Yokomaku, Y; Ishizaki, K; Kito, S; Sezaki, T; Hayashi, G; Murakami, H.
  • Kondo T; Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
  • Iwatani Y; Department of Infectious Diseases and Immunology, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
  • Matsuoka K; Division of Basic Medicine, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
  • Fujino T; Department of Infectious Diseases and Immunology, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
  • Umemoto S; Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
  • Yokomaku Y; Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
  • Ishizaki K; Department of Infectious Diseases and Immunology, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
  • Kito S; Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
  • Sezaki T; Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
  • Hayashi G; Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
  • Murakami H; Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Japan.
Sci Adv ; 6(42)2020 10.
Article in English | MEDLINE | ID: covidwho-781066
ABSTRACT
To combat severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) and any unknown emerging pathogens in the future, the development of a rapid and effective method to generate high-affinity antibodies or antibody-like proteins is of critical importance. We here report high-speed in vitro selection of multiple high-affinity antibody-like proteins against various targets including the SARS-CoV-2 spike protein. The sequences of monobodies against the SARS-CoV-2 spike protein were successfully procured within only 4 days. Furthermore, the obtained monobody efficiently captured SARS-CoV-2 particles from the nasal swab samples of patients and exhibited a high neutralizing activity against SARS-CoV-2 infection (half-maximal inhibitory concentration, 0.5 nanomolar). High-speed in vitro selection of antibody-like proteins is a promising method for rapid development of a detection method for, and of a neutralizing protein against, a virus responsible for an ongoing, and possibly a future, pandemic.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Peptidyl-Dipeptidase A / Single-Domain Antibodies / Spike Glycoprotein, Coronavirus / Betacoronavirus Language: English Year: 2020 Document Type: Article Affiliation country: Sciadv.abd3916

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Peptidyl-Dipeptidase A / Single-Domain Antibodies / Spike Glycoprotein, Coronavirus / Betacoronavirus Language: English Year: 2020 Document Type: Article Affiliation country: Sciadv.abd3916