4.4 Article

Synthetic proteins for COVID-19 diagnostics

期刊

PEPTIDES
卷 143, 期 -, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.peptides.2021.170583

关键词

COVID-19 variants; Structure based design; Receptor binding domain; S protein epitopes; ACE2 interaction; Peptide vaccines; Neutralizing antibodies

资金

  1. LDRD ER funding
  2. NIAID [R01 AI137332]

向作者/读者索取更多资源

A small, synthetic protein JS7 has been identified as a potential basis for specific diagnostics for SARS-CoV-2 infections, with associations found in sera from COVID-19 patients. By analyzing the binding between various antibodies and JS7, assessments can be made based on disease severity and clinical outcomes.
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 E484K or N501Y, can be quickly synthesized in 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.

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