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Neutralizing Aptamers Block S/RBD-ACE2 Interactions and Prevent Host Cell Infection.
Liu, Xiaohui; Wang, Yi-Ling; Wu, Jacky; Qi, Jianjun; Zeng, Zihua; Wan, Quanyuan; Chen, Zhenghu; Manandhar, Pragya; Cavener, Victoria S; Boyle, Nina R; Fu, Xinping; Salazar, Eric; Kuchipudi, Suresh V; Kapur, Vivek; Zhang, Xiaoliu; Umetani, Michihisa; Sen, Mehmet; Willson, Richard C; Chen, Shu-Hsia; Zu, Youli.
Afiliação
  • Liu X; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
  • Wang YL; Center for Immunotherapy Research, Houston Methodist Research Institute, Houston, TX, 77030, USA.
  • Wu J; Department of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signalling, University of Houston, Houston, TX, 77204, USA.
  • Qi J; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
  • Zeng Z; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
  • Wan Q; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
  • Chen Z; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
  • Manandhar P; Department of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA.
  • Cavener VS; Animal Diagnostic Laboratory, Dept. of Veterinary and Biomedical Sciences, Huck Institutes of Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
  • Boyle NR; Animal Diagnostic Laboratory, Dept. of Veterinary and Biomedical Sciences, Huck Institutes of Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
  • Fu X; Department of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signalling, University of Houston, Houston, TX, 77204, USA.
  • Salazar E; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
  • Kuchipudi SV; Animal Diagnostic Laboratory, Dept. of Veterinary and Biomedical Sciences, Huck Institutes of Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
  • Kapur V; Dept. of Animal Science and Huck Institutes of Life Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
  • Zhang X; Department of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signalling, University of Houston, Houston, TX, 77204, USA.
  • Umetani M; Department of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signalling, University of Houston, Houston, TX, 77204, USA.
  • Sen M; Department of Biology and Biochemistry, University of Houston, Houston, TX, 77204, USA.
  • Willson RC; Chemical and Biomolecular Engineering, University of Houston, Houston, TX, 77204, USA.
  • Chen SH; Center for Immunotherapy Research, Houston Methodist Research Institute, Houston, TX, 77030, USA.
  • Zu Y; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, 77030, USA.
Angew Chem Int Ed Engl ; 60(18): 10273-10278, 2021 04 26.
Article em En | MEDLINE | ID: mdl-33684258
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Aptâmeros de Nucleotídeos / Glicoproteína da Espícula de Coronavírus / Enzima de Conversão de Angiotensina 2 / SARS-CoV-2 / Tratamento Farmacológico da COVID-19 Limite: Humans Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Aptâmeros de Nucleotídeos / Glicoproteína da Espícula de Coronavírus / Enzima de Conversão de Angiotensina 2 / SARS-CoV-2 / Tratamento Farmacológico da COVID-19 Limite: Humans Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos