| Literature DB >> 34087220 |
Catherine H Schein1, Corri B Levine2, Susan L F McLellan3, Surendra S Negi4, Werner Braun4, Stephen C Dreskin5, Elizabeth S Anaya6, Jurgen Schmidt6.
Abstract
There is an urgent need for inexpensive, rapid and specific antigen-based assays to test for vaccine efficacy and detect infection with SARS-CoV-2 and its variants. We have identified a small, synthetic protein (JS7), representing a region of maximum variability within the receptor binding domain (RBD), which binds antibodies in sera from nine patients with PCR-verified COVID-19 of varying severity. Antibodies binding to either JS7 or the SARS-CoV-2 recombinant RBD, as well as those that disrupt binding between a fragment of the ACE2 receptor and the RBD, are proportional to disease severity and clinical outcome. Binding to JS7 was inhibited by linear peptides from the RBD interface with ACE2. Variants of JS7, such as E484 K or N501Y, can be quickly synthesized in a pure form in large quantities by automated methods. JS7 and related synthetic antigens can provide a basis for specific diagnostics for SARS-CoV-2 infections.Entities:
Keywords: ACE2 interaction; COVID-19 variants; Receptor binding domain; S protein epitopes; Structure based design; Synthetic proteins
Year: 2021 PMID: 34087220 DOI: 10.1016/j.peptides.2021.170583
Source DB: PubMed Journal: Peptides ISSN: 0196-9781 Impact factor: 3.750