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Broadly Neutralizing Aptamers to SARS-CoV-2: A Diverse Panel of Modified DNA Antiviral Agents

Abstract

Since its discovery, COVID-19 has rapidly spread across the globe and has had a massive toll on human health, with infection mortality rates as high as 10%, and a crippling impact on the world economy. Despite numerous advances, there remains an urgent need for accurate and rapid point-of-care diagnostic tests and better therapeutic treatment options. To contribute chemically distinct, non-protein-based affinity reagents, we report here the identification of modified DNA-based aptamers that selectively bind to the S1, S2, or receptor-binding domain of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Several aptamers inhibit the binding of the spike protein to its cell-surface receptor angiotensin-converting enzyme 2 (ACE2) and neutralize authentic SARS-CoV-2 virus , including all variants of concern. With a high degree of nuclease resistance imparted by the base modifications, these reagents represent a new class of molecules with potential for further development as diagnostics or therapeutics.

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References
1.
Raval S, Sarpe V, Hepburn M, Crowder D, Zhang T, Viner R . Improving Spectral Validation Rates in Hydrogen-Deuterium Exchange Data Analysis. Anal Chem. 2021; 93(9):4246-4254. DOI: 10.1021/acs.analchem.0c05045. View

2.
Dey A, Khati M, Tang M, Wyatt R, Lea S, James W . An aptamer that neutralizes R5 strains of human immunodeficiency virus type 1 blocks gp120-CCR5 interaction. J Virol. 2005; 79(21):13806-10. PMC: 1262572. DOI: 10.1128/JVI.79.21.13806-13810.2005. View

3.
Rey M, Sarpe V, Burns K, Buse J, Baker C, van Dijk M . Mass spec studio for integrative structural biology. Structure. 2014; 22(10):1538-48. PMC: 4391204. DOI: 10.1016/j.str.2014.08.013. View

4.
Tao K, Tzou P, Nouhin J, Gupta R, de Oliveira T, Kosakovsky Pond S . The biological and clinical significance of emerging SARS-CoV-2 variants. Nat Rev Genet. 2021; 22(12):757-773. PMC: 8447121. DOI: 10.1038/s41576-021-00408-x. View

5.
Cox J, Neuhauser N, Michalski A, Scheltema R, Olsen J, Mann M . Andromeda: a peptide search engine integrated into the MaxQuant environment. J Proteome Res. 2011; 10(4):1794-805. DOI: 10.1021/pr101065j. View