Synthetic Heparan Sulfate Mimetic Pixatimod (PG545) Potently Inhibits SARS-CoV-2 by Disrupting the Spike-ACE2 Interaction

Research output: Contribution to journalJournal articleResearchpeer-review

Documents

  • Fulltext

    Final published version, 5.14 MB, PDF document

  • Scott E. Guimond
  • Courtney J. Mycroft-West
  • Neha S. Gandhi
  • Julia A. Tree
  • Thuy T. Le
  • C. Mirella Spalluto
  • Maria V. Humbert
  • Karen R. Buttigieg
  • Naomi Coombes
  • Michael J. Elmore
  • Matthew Wand
  • Kristina Nyström
  • Joanna Said
  • Yin Xiang Setoh
  • Alberto A. Amarilla
  • Naphak Modhiran
  • Julian D.J. Sng
  • Mohit Chhabra
  • Paul R. Young
  • Daniel J. Rawle
  • Marcelo A. Lima
  • Edwin A. Yates
  • Richard Karlsson
  • James Stewart
  • Dung Nguyen
  • Stephen Laidlaw
  • Edward Hammond
  • Keith Dredge
  • Tom M.A. Wilkinson
  • Daniel Watterson
  • Alexander A. Khromykh
  • Andreas Suhrbier
  • Miles W. Carroll
  • Edward Trybala
  • Tomas Bergström
  • Vito Ferro
  • Mark A. Skidmore

Heparan sulfate (HS) is a cell surface polysaccharide recently identified as a coreceptor with the ACE2 protein for the S1 spike protein on SARS-CoV-2 virus, providing a tractable new therapeutic target. Clinically used heparins demonstrate an inhibitory activity but have an anticoagulant activity and are supply-limited, necessitating alternative solutions. Here, we show that synthetic HS mimetic pixatimod (PG545), a cancer drug candidate, binds and destabilizes the SARS-CoV-2 spike protein receptor binding domain and directly inhibits its binding to ACE2, consistent with molecular modeling identification of multiple molecular contacts and overlapping pixatimod and ACE2 binding sites. Assays with multiple clinical isolates of SARS-CoV-2 virus show that pixatimod potently inhibits the infection of monkey Vero E6 cells and physiologically relevant human bronchial epithelial cells at safe therapeutic concentrations. Pixatimod also retained broad potency against variants of concern (VOC) including B.1.1.7 (Alpha), B.1.351 (Beta), B.1.617.2 (Delta), and B.1.1.529 (Omicron). Furthermore, in a K18-hACE2 mouse model, pixatimod significantly reduced SARS-CoV-2 viral titers in the upper respiratory tract and virus-induced weight loss. This demonstration of potent anti-SARS-CoV-2 activity tolerant to emerging mutations establishes proof-of-concept for targeting the HS-Spike protein-ACE2 axis with synthetic HS mimetics and provides a strong rationale for clinical investigation of pixatimod as a potential multimodal therapeutic for COVID-19.

Original languageEnglish
JournalACS Central Science
Volume8
Issue number5
Pages (from-to)527-545
Number of pages19
ISSN2374-7943
DOIs
Publication statusPublished - 2022

Bibliographical note

Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.

ID: 342927703