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NMR Based SARS-CoV-2 Antibody Screening

  • Marta V. Schoenle
  • , Yang Li
  • , Meng Yuan
  • , Michael W. Clarkson
  • , Ian A. Wilson
  • , Wolfgang Peti
  • , Rebecca Page
  • University of Arizona
  • University of Connecticut
  • Scripps Research Institute

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) entry into cells is a complex process that involves (1) recognition of the host entry receptor, angiotensin-converting enzyme 2 (ACE2), by the SARS-CoV-2 spike protein receptor binding domain (RBD), and (2) the subsequent fusion of the viral and cell membranes. Our long-term immune-defense is the production of antibodies (Abs) that recognize the SARS-CoV-2 RBD and successfully block viral infection. Thus, to understand immunity against SARS-CoV-2, a comprehensive molecular understanding of how human SARS-CoV-2 Abs recognize the RBD is needed. Here, we report the sequence-specific backbone assignment of the SARS-CoV-2 RBD and, furthermore, demonstrate that biomolecular NMR spectroscopy chemical shift perturbation (CSP) mapping successfully and rapidly identifies the molecular epitopes of RBD-specific mAbs. By incorporating NMR-based CSP mapping with other molecular techniques to define RBD-mAb interactions and then correlating these data with neutralization efficacy, structure-based approaches for developing improved vaccines and COVID-19 mAb-based therapies will be greatly accelerated.

Original languageEnglish
Pages (from-to)7930-7934
Number of pages5
JournalJournal of the American Chemical Society
Volume143
Issue number21
DOIs
Publication statusPublished - 21 May 2021
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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