Viruses (Mar 2022)

A Palmitic Acid-Conjugated, Peptide-Based pan-CoV Fusion Inhibitor Potently Inhibits Infection of SARS-CoV-2 Omicron and Other Variants of Concern

  • Qiaoshuai Lan,
  • Jasper Fuk-Woo Chan,
  • Wei Xu,
  • Lijue Wang,
  • Fanke Jiao,
  • Guangxu Zhang,
  • Jing Pu,
  • Jie Zhou,
  • Shuai Xia,
  • Lu Lu,
  • Kwok-Yung Yuen,
  • Shibo Jiang,
  • Qian Wang

DOI
https://doi.org/10.3390/v14030549
Journal volume & issue
Vol. 14, no. 3
p. 549

Abstract

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Our previous studies have shown that cholesterol-conjugated, peptide-based pan-coronavirus (CoV) fusion inhibitors can potently inhibit human CoV infection. However, only palmitic acid (C16)-based lipopeptide drugs have been tested clinically, suggesting that the development of C16-based lipopeptide drugs is feasible. Here, we designed and synthesized a C16-modified pan-CoV fusion inhibitor, EK1-C16, and found that it potently inhibited infection by SARS-CoV-2 and its variants of concern (VOCs), including Omicron, and other human CoVs and bat SARS-related CoVs (SARSr-CoVs). These results suggest that EK1-C16 could be further developed for clinical use to prevent and treat infection by the currently circulating MERS-CoV, SARS-CoV-2 and its VOCs, as well as any future emerging or re-emerging coronaviruses.

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