《Science,7月23日,Structural basis for neutralization of SARS-CoV-2 and SARS-CoV by a potent therapeutic antibody》

  • 来源专题:COVID-19科研动态监测
  • 编译者: zhangmin
  • 发布时间:2020-07-28
  • Structural basis for neutralization of SARS-CoV-2 and SARS-CoV by a potent therapeutic antibody

    Zhe Lv1,8,*, Yong-Qiang Deng2,*, Qing Ye2,*, Lei Cao1,*, Chun-Yun Sun3,*, Changfa Fan4,*, Weijin Hua

    Science 23 Jul 2020:

    eabc5881

    DOI: 10.1126/science.abc5881

    Abstract

    The COVID-19 pandemic caused by the SARS-CoV-2 virus has resulted in an unprecedented public health crisis. There are no approved vaccines or therapeutics for treating COVID-19. Here we reported a humanized monoclonal antibody, H014, efficiently neutralizes SARS-CoV-2 and SARS-CoV pseudoviruses as well as authentic SARS-CoV-2 at nM level by engaging the S receptor binding domain (RBD). Importantly, H014 administration reduced SARS-CoV-2 titers in the infected lungs and prevented pulmonary pathology in hACE2 mouse model. Cryo-EM characterization of the SARS-CoV-2 S trimer in complex with the H014 Fab fragment unveiled a novel conformational epitope, which is only accessible when the RBD is in open conformation. Biochemical, cellular, virological and structural studies demonstrated that H014 prevents attachment of SARS-CoV-2 to its host cell receptors. Epitope analysis of available neutralizing antibodies against SARS-CoV and SARS-CoV-2 uncover broad cross-protective epitopes. Our results highlight a key role for antibody-based therapeutic interventions in the treatment of COVID-19.

  • 原文来源:https://science.sciencemag.org/content/early/2020/07/22/science.abc5881
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    • 来源专题:COVID-19科研动态监测
    • 编译者:xuwenwhlib
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    • 编译者:zhangmin
    • 发布时间:2020-07-28
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