Synthetic proteins for COVID-19 diagnostics

被引:4
|
作者
Schein, Catherine H. [1 ,2 ]
Levine, Corri B. [3 ]
McLellan, Susan L. F. [4 ]
Negi, Surendra S. [1 ,5 ]
Braun, Werner [1 ,2 ,5 ]
Dreskin, Stephen C. [6 ]
Anaya, Elizabeth S. [7 ]
Schmidt, Jurgen [7 ]
机构
[1] Univ Texas Med Branch, Dept Biochem & Mol Biol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Inst Human Infect & Immun IHII, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, Inst Translat Sci, Galveston, TX 77555 USA
[4] Univ Texas Med Branch, Dept Internal Med Infect Dis, Galveston, TX 77555 USA
[5] Univ Texas Med Branch, Sealy Ctr Struct Biol & Mol Biophys, Galveston, TX 77555 USA
[6] Univ Colorado Denver, Dept Med, Div Allergy & Clin Immunol, Aurora, CO 80045 USA
[7] Los Alamos Natl Lab, Biosci Div, Bioenergy & Biome Sci B 11, Los Alamos, NM USA
关键词
COVID-19; variants; Structure based design; Receptor binding domain; S protein epitopes; ACE2; interaction; Peptide vaccines; Neutralizing antibodies; SECONDARY STRUCTURE; SPIKE; RECEPTOR; BINDING; ANTIBODIES; PEPTIDES;
D O I
10.1016/j.peptides.2021.170583
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:9
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