Synthetic Neutralizing Peptides Inhibit the Host Cell Binding of Spike Protein and Block Infection of SARS-CoV-2.

Abstract

Antiviral treatments of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been extensively pursued to conquer the pandemic. To inhibit the viral entry to the host cell, we designed and obtained three peptide sequences via quartz crystal microbalance measurement screening, which showed high affinity at nanomole to the S1 subunit of the spike protein and wild-type SARS-CoV-2 pseudovirus. Circular dichroism spectroscopy measurements revealed significant conformation changes of the S1 protein upon encounter with the three peptides. The peptides were able to effectively block the infection of a pseudovirus to 50% by inhibiting the host cell lines binding with the S1 protein, evidenced by the results from Western blotting and pseudovirus luciferase assay. Moreover, the combination of the three peptides could increase the inhibitory rate to 75%. In conclusion, the three chemically synthetic neutralizing peptides and their combinations hold promising potential as effective therapeutics in the prevention and treatment of COVID-19.

• Authors: Tao Wang, Xiaocui Fang, Tao Wen, Jian Liu, Zhaoyi Zhai, Zhiyou Wang, Jie Meng, Yanlian Yang, Chen Wang, Haiyan Xu
• Journal: Journal of medicinal chemistry (J Med Chem) Vol. 64 Issue 19 Pg. 14887-14894 (10 14 2021) ISSN: 1520-4804 [Electronic] United States
• PMID: 34533959 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Peptides
• Protein Subunits
• Spike Glycoprotein, Coronavirus
• spike protein, SARS-CoV-2
• ACE2 protein, human
• Angiotensin-Converting Enzyme 2

Topics

• A549 Cells
• Angiotensin-Converting Enzyme 2 (chemistry, metabolism)
• COVID-19 (pathology, virology)
• Cell Survival (drug effects)
• Circular Dichroism
• Humans
• Neutralization Tests
• Peptides (chemistry, metabolism, pharmacology)
• Protein Binding
• Protein Subunits (chemistry, metabolism)
• SARS-CoV-2 (isolation & purification)
• Spike Glycoprotein, Coronavirus (chemistry, metabolism)
• Virus Internalization (drug effects)