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

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.
Mesh Terms:
Angiotensin-Converting Enzyme 2, Antiviral Agents, Aptamers, Nucleotide, Base Sequence, COVID-19, COVID-19 Drug Treatment, HEK293 Cells, Humans, Protein Interaction Domains and Motifs, Protein Interaction Maps, SARS-CoV-2, Spike Glycoprotein, Coronavirus
Angew Chem Int Ed Engl
Date: Apr. 26, 2021
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