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Potent neutralization of 2019 novel coronavirus by recombinant ACE2-Ig
Changhai Lei; Wenyan Fu; Kewen Qian; Tian Li; Sheng Zhang; Min Ding; Shi Hu.
Affiliation
  • Changhai Lei; Second Military Medical University
  • Wenyan Fu; Shanghai Jiao Tong University School of Medicine
  • Kewen Qian; Second Military Medical University
  • Tian Li; Second Military Medical University
  • Sheng Zhang; Shanghai Jiao Tong University School of Medicine
  • Min Ding; Pharchoice Therapeutics Inc
  • Shi Hu; Second Militarily Medical University
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-929976
ABSTRACT
2019-nCoV, which is a novel coronavirus emerged in Wuhan, China, at the end of 2019, has caused at least infected 11,844 as of Feb 1, 2020. However, there is no specific antiviral treatment or vaccine currently. Very recently report had suggested that novel CoV would use the same cell entry receptor, ACE2, as the SARS-CoV. In this report, we generated a novel recombinant protein by connecting the extracellular domain of human ACE2 to the Fc region of the human immunoglobulin IgG1. An ACE2 mutant with low catalytic activity was also used in the study. The fusion proteins were then characterized. Both fusion proteins has high affinity binding to the receptor-binding domain (RBD) of SARS-CoV and 2019-nCoV and exerted desired pharmacological properties. Moreover, fusion proteins potently neutralized SARS-CoV and 2019-nCoV in vitro. As these fusion proteins exhibit cross-reactivity against coronaviruses, they could have potential applications for diagnosis, prophylaxis, and treatment of 2019-nCoV.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Type of study: Rct Language: En Year: 2020 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Type of study: Rct Language: En Year: 2020 Document type: Preprint