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Broadly neutralizing and protective nanobodies against diverse sarbecoviruses
Mingxi Li; Yifei Ren; Zhen Qin Aw; Bo Chen; Ziqing Yang; Yuqing Lei; Qingtai Liang; Junxian Hong; Yiling Yang; Jing Chen; Yi Hao Wong; Sisi Shan; Senyan Zhang; Jiwan Ge; Ruoke Wang; Xuanling Shi; Qi Zhang; Justin Jang Hann Chu; Xinquan Wang; Linqi Zhang.
Affiliation
  • Mingxi Li; Tsinghua University
  • Yifei Ren; Tsinghua University
  • Zhen Qin Aw; National University of Singapore
  • Bo Chen; NB BIOLAB Co. Ltd, Chengdu, China
  • Ziqing Yang; Tsinghua University
  • Yuqing Lei; Tsinghua University
  • Qingtai Liang; Tsinghua University
  • Junxian Hong; Tsinghua University
  • Yiling Yang; Tsinghua University
  • Jing Chen; Tsinghua University
  • Yi Hao Wong; National University of Singapore
  • Sisi Shan; Tsinghua University
  • Senyan Zhang; Tsinghua University
  • Jiwan Ge; Tsinghua University
  • Ruoke Wang; Tsinghua University
  • Xuanling Shi; Tsinghua University
  • Qi Zhang; Tsinghua University
  • Justin Jang Hann Chu; National University of Singapore
  • Xinquan Wang; Tsinghua University
  • Linqi Zhang; Tsinghua University
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-488087
ABSTRACT
As SARS-CoV-2 Omicron and other variants of concern continue spreading around the world, development of antibodies and vaccines to confer broad and protective activity is a global priority. Here, we report on the identification of a special group of nanobodies from immunized alpaca with exceptional breadth and potency against diverse sarbecoviruses including SARS-CoV-1, Omicron BA.1, and BA.2. Crystal structure analysis of one representative nanobody, 3-2A2-4, revealed a highly conserved epitope between the cryptic and the outer face of the receptor binding domain (RBD). The epitope is readily accessible regardless of RBD in "up" or "down" conformation and distinctive from the receptor ACE2 binding site. Passive delivery of 3-2A2-4 protected K18-hACE2 mice from infection of authentic SARS-CoV-2 Delta and Omicron. This group of nanobodies and the epitope identified should provide invaluable reference for the development of next generation antibody therapies and vaccines against wide varieties of SARS-CoV-2 infection and beyond.
License
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Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2022 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2022 Document type: Preprint