Neutralizing Aptamers Block S/RBD-ACE2 Interactions and Prevent Host Cell Infection

Angew Chem Int Ed Engl. 2021 Apr 26;60(18):10273-10278. doi: 10.1002/anie.202100345. Epub 2021 Mar 22.

Abstract

The receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 spike (S) protein plays a central role in mediating the first step of virus infection to cause disease: virus binding to angiotensin-converting enzyme 2 (ACE2) receptors on human host cells. Therefore, S/RBD is an ideal target for blocking and neutralization therapies to prevent and treat coronavirus disease 2019 (COVID-19). Using a target-based selection approach, we developed oligonucleotide aptamers containing a conserved sequence motif that specifically targets S/RBD. Synthetic aptamers had high binding affinity for S/RBD-coated virus mimics (KD ≈7 nM) and also blocked interaction of S/RBD with ACE2 receptors (IC50 ≈5 nM). Importantly, aptamers were able to neutralize S protein-expressing viral particles and prevent host cell infection, suggesting a promising COVID-19 therapy strategy.

Keywords: COVID-19; SARS-CoV-2; aptamers; receptor-binding domain (RBD); virus neutralization.

MeSH terms

  • Angiotensin-Converting Enzyme 2 / metabolism*
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Aptamers, Nucleotide / chemistry
  • Aptamers, Nucleotide / pharmacology*
  • Base Sequence
  • COVID-19 / metabolism
  • COVID-19 Drug Treatment*
  • HEK293 Cells
  • Humans
  • Protein Interaction Domains and Motifs / drug effects
  • Protein Interaction Maps / drug effects
  • SARS-CoV-2 / chemistry
  • SARS-CoV-2 / drug effects*
  • SARS-CoV-2 / physiology
  • Spike Glycoprotein, Coronavirus / chemistry
  • Spike Glycoprotein, Coronavirus / metabolism*

Substances

  • Antiviral Agents
  • Aptamers, Nucleotide
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2