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10.1016/j.pep.2021.105861

http://scihub22266oqcxt.onion/10.1016/j.pep.2021.105861
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suck abstract from ncbi

pmid33667651      Protein+Expr+Purif 2021 ; 183 (?): 105861
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  • Expression of SARS-CoV-2 surface glycoprotein fragment 319-640 in E coli, and its refolding and purification #MMPMID33667651
  • Fitzgerald GA; Komarov A; Kaznadzey A; Mazo I; Kireeva ML
  • Protein Expr Purif 2021[Jul]; 183 (?): 105861 PMID33667651show ga
  • Sensitive and specific serology tests are essential for epidemiological and public health studies of COVID-19 and for vaccine efficacy testing. The presence of antibodies to SARS-CoV-2 surface glycoprotein (Spike) and, specifically, its receptor-binding domain (RBD) correlates with inhibition of SARS-CoV-2 binding to the cellular receptor and viral entry into the cells. Serology tests that detect antibodies targeting RBD have high potential to predict COVID-19 immunity and to accurately determine the extent of the vaccine-induced immune response. Cost-effective methods of expression and purification of Spike and its fragments that preserve antigenic properties are essential for development of such tests. Here we describe a method of production of His6-tagged S319-640 fragment containing RBD in E. coli. It includes expression of the fragment, solubilization of inclusion bodies, and on-the-column refolding. The antigenic properties of the resulting product are similar, but not identical to the RBD-containing fragment expressed in human cells.
  • |Binding Sites[MESH]
  • |COVID-19/*virology[MESH]
  • |Cloning, Molecular[MESH]
  • |Escherichia coli/chemistry/genetics[MESH]
  • |Gene Expression[MESH]
  • |Humans[MESH]
  • |Peptide Fragments/chemistry/genetics/isolation & purification[MESH]
  • |Protein Domains[MESH]
  • |Protein Refolding[MESH]
  • |SARS-CoV-2/*chemistry/genetics[MESH]
  • |Solubility[MESH]


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