| Literature DB >> 33684258 |
Xiaohui Liu1, Yi-Ling Wang2, Jacky Wu3, Jianjun Qi1, Zihua Zeng1, Quanyuan Wan1, Zhenghu Chen1, Pragya Manandhar4, Victoria S Cavener5, Nina R Boyle5, Xinping Fu3, Eric Salazar1, Suresh V Kuchipudi5, Vivek Kapur6, Xiaoliu Zhang3, Michihisa Umetani3, Mehmet Sen4, Richard C Willson7, Shu-Hsia Chen2, Youli Zu1.
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.Entities:
Keywords: COVID-19; SARS-CoV-2; aptamers; receptor-binding domain (RBD); virus neutralization
Year: 2021 PMID: 33684258 DOI: 10.1002/anie.202100345
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336