Your browser doesn't support javascript.
loading
An ultrapotent RBD-targeted biparatopic nanobody neutralizes broad SARS-CoV-2 variants
Xiaojing Chi; Xinhui Zhang; Shengnan Pan; Yanying Yu; Tianli Lin; Huarui Duan; Xiuying Liu; Wenfang Chen; Xuehua Yang; Qiang Ding; Jianwei Wang; Wei Yang.
Afiliación
  • Xiaojing Chi; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Xinhui Zhang; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Shengnan Pan; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Yanying Yu; School of Medicine, Tsinghua University
  • Tianli Lin; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Huarui Duan; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Xiuying Liu; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Wenfang Chen; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Xuehua Yang; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Qiang Ding; School of Medicine, Tsinghua University
  • Jianwei Wang; Institute of Pathogen Biology, Chinese Academy of Medical Sciences
  • Wei Yang; Chinese Academy of Medical Sciences
Preprint en En | PREPRINT-BIORXIV | ID: ppbiorxiv-474052
ABSTRACT
The wide transmission and host adaptation of SARS-CoV-2 have led to the rapid accumulation of mutations, posing significant challenges to the effectiveness of vaccines and therapeutic antibodies. Although several neutralizing antibodies were authorized for emergency clinical use, convalescent patients derived natural antibodies are vulnerable to SARS-CoV-2 Spike mutation. Here, we describe the screen of a panel of SARS-CoV-2 receptor-binding domain (RBD) targeted nanobodies (Nbs) from a synthetic library and the design of a biparatopic Nb, named Nb1-Nb2, with tight affinity and super wide neutralization breadth against multiple SARS-CoV-2 variants of concern. Deep-mutational scanning experiments identify the potential binding epitopes of the Nbs on the RBD and demonstrate that biparatopic Nb1-Nb2 has a strong escape resistant feature against more than 60 tested RBD amino acid substitutions. Using pseudovirion-based and trans-complementation SARS-CoV-2 tools, we determine that the Nb1-Nb2 broadly neutralizes multiple SARS-CoV-2 variants, including Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2), Lambda (C.37), Kappa (B.1.617.1) and Mu (B.1.621). Furthermore, a heavy chain antibody is constructed by fusing the human IgG1 Fc to Nb1-Nb2 (designated as Nb1-Nb2-Fc) to improve its neutralization potency, yield, stability and potential half-life extension. For the new Omicron variant (B.1.1.529) that harbors unprecedented multiple RBD mutations, Nb1-Nb2-Fc keeps a firm affinity (KD < 1.0x10-12 M) and strong neutralizing activity (IC50 = 0.0017 nM). Together, we developed a tetravalent biparatopic human heavy chain antibody with ultrapotent and broad-spectrum SARS-CoV-2 neutralization activity which highlights the potential clinical applications.
Licencia
cc_no
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Preprint