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Camel nanobodies broadly neutralize SARS-CoV-2 variants
Jessica Hong; Hyung Joon Kwon; Raul Cachau; Catherine Z Chen; Kevin John Butay; Zhijian Duan; Dan Li; Hua Ren; Tianyuzhou Liang; Jianghai Zhu; Venkata P Dandey; Negin P. Martin; Dominic Esposito; Uriel Ortega-Rodriguez; Miao Xu; Mario J. Borgnia; Hang Xie; Mitchell Ho.
Afiliação
  • Jessica Hong; National Cancer Institute
  • Hyung Joon Kwon; United States Food and Drug Administration
  • Raul Cachau; Leidos Biomedical Research, Inc.
  • Catherine Z Chen; National Center for Advancing Translational Sciences
  • Kevin John Butay; National Institute of Environmental Health Sciences
  • Zhijian Duan; National Cancer Institute
  • Dan Li; National Cancer Institute
  • Hua Ren; National Cancer Institute
  • Tianyuzhou Liang; National Cancer Institute
  • Jianghai Zhu; Leidos Biomedical Research, Inc.
  • Venkata P Dandey; National Institute of Environmental Health Sciences
  • Negin P. Martin; National Institute of Environmental Health Sciences (NIEHS)
  • Dominic Esposito; Frederick National Lab for Cancer Research
  • Uriel Ortega-Rodriguez; United States Food and Drug Administration
  • Miao Xu; National Center for Advancing Translational Sciences
  • Mario J. Borgnia; National Institute of Health
  • Hang Xie; Center for Biologics Evaluation and Research, US Food and Drug Administration
  • Mitchell Ho; National Cancer Institute, NIH
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-465996
ABSTRACT
With the emergence of SARS-CoV-2 variants, there is urgent need to develop broadly neutralizing antibodies. Here, we isolate two VHH nanobodies (7A3 and 8A2) from dromedary camels by phage display, which have high affinity for the receptor-binding domain (RBD) and broad neutralization activities against SARS-CoV-2 and its emerging variants. Cryo-EM complex structures reveal that 8A2 binds the RBD in its up mode and 7A3 inhibits receptor binding by uniquely targeting a highly conserved and deeply buried site in the spike regardless of the RBD conformational state. 7A3 at a dose of [≥]5 mg/kg efficiently protects K18-hACE2 transgenic mice from the lethal challenge of B.1.351 or B.1.617.2, suggesting that the nanobody has promising therapeutic potentials to curb the COVID-19 surge with emerging SARS-CoV-2 variants. One-Sentence SummaryDromedary camel (Camelus dromedarius) VHH phage libraries were built for isolation of the nanobodies that broadly neutralize SARS-CoV-2 variants.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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