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Molecular probes of spike ectodomain and its subdomains for SARS-CoV-2 variants, Alpha through Omicron.
Teng, I-Ting; Nazzari, Alexandra F; Choe, Misook; Liu, Tracy; Oliveira de Souza, Matheus; Petrova, Yuliya; Tsybovsky, Yaroslav; Wang, Shuishu; Zhang, Baoshan; Artamonov, Mykhaylo; Madan, Bharat; Huang, Aric; Lopez Acevedo, Sheila N; Pan, Xiaoli; Ruckwardt, Tracy J; DeKosky, Brandon J; Mascola, John R; Misasi, John; Sullivan, Nancy J; Zhou, Tongqing; Kwong, Peter D.
Affiliation
  • Teng IT; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Nazzari AF; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Choe M; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Liu T; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Oliveira de Souza M; Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
  • Petrova Y; Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts, United States of America.
  • Tsybovsky Y; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Wang S; Electron Microscopy Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research Sponsored by the National Cancer Institute, Frederick, Maryland, United States of America.
  • Zhang B; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Artamonov M; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Madan B; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Huang A; Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
  • Lopez Acevedo SN; Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts, United States of America.
  • Pan X; Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
  • Ruckwardt TJ; Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
  • DeKosky BJ; Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
  • Mascola JR; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
  • Misasi J; Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas, United States of America.
  • Sullivan NJ; Ragon Institute of MGH, MIT, and Harvard, Cambridge, Massachusetts, United States of America.
  • Zhou T; Department of Chemical Engineering, The University of Kansas, Lawrence, Kansas, United States of America.
  • Kwong PD; Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
PLoS One ; 17(5): e0268767, 2022.
Article in En | MEDLINE | ID: mdl-35609088
Since the outbreak of the COVID-19 pandemic, widespread infections have allowed SARS-CoV-2 to evolve in human, leading to the emergence of multiple circulating variants. Some of these variants show increased resistance to vaccine-elicited immunity, convalescent plasma, or monoclonal antibodies. In particular, mutations in the SARS-CoV-2 spike have drawn attention. To facilitate the isolation of neutralizing antibodies and the monitoring of vaccine effectiveness against these variants, we designed and produced biotin-labeled molecular probes of variant SARS-CoV-2 spikes and their subdomains, using a structure-based construct design that incorporated an N-terminal purification tag, a specific amino acid sequence for protease cleavage, the variant spike-based region of interest, and a C-terminal sequence targeted by biotin ligase. These probes could be produced by a single step using in-process biotinylation and purification. We characterized the physical properties and antigenicity of these probes, comprising the N-terminal domain (NTD), the receptor-binding domain (RBD), the RBD and subdomain 1 (RBD-SD1), and the prefusion-stabilized spike ectodomain (S2P) with sequences from SARS-CoV-2 variants of concern or of interest, including variants Alpha, Beta, Gamma, Epsilon, Iota, Kappa, Delta, Lambda, Mu, and Omicron. We functionally validated probes by using yeast expressing a panel of nine SARS-CoV-2 spike-binding antibodies and confirmed sorting capabilities of variant probes using yeast displaying libraries of plasma antibodies from COVID-19 convalescent donors. We deposited these constructs to Addgene to enable their dissemination. Overall, this study describes a matrix of SARS-CoV-2 variant molecular probes that allow for assessment of immune responses, identification of serum antibody specificity, and isolation and characterization of neutralizing antibodies.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos