<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schwarze M</submitter><funding>Deutsche Forschungsgemeinschaft (DFG)</funding><funding>European Regional Development Fund (ERDF) and the Free State of Saxony</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>European Union, the European Regional Development Fund (ERDF) and the Free State of Saxony</funding><funding>Open Access Publishing Fund of Leipzig University</funding><pagination>1515</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9782079</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(12)</volume><pubmed_abstract>This study investigated the IgG and IgA antibody response against recombinant S1 and receptor binding domains (RBD) of the spike (S-) protein and the membrane (M-) protein using a set of 115 serum samples collected from patients infected with SARS-CoV-2 in Germany before April 2021 using protein and peptide ELISA. As S1- and RBD-proteins expressed in &lt;i>Escherichia coli&lt;/i> provided poor sensitivities in ELISA, they were replaced by proteins expressed in HEK cells. The RBD-ELISA provided a sensitivity of 90.6% (N = 85) for samples collected from patients with confirmed SARS-CoV-2 infections more than 14 days after symptom onset or a positive PCR test. In population-based controls, the specificity was 97.9% (N = 94). In contrast, the sensitivities were only 41.2% and 72.6% for M- and N-prot</pubmed_abstract><journal>Pathogens (Basel, Switzerland)</journal><pubmed_title>Evaluation of S- and M-Proteins Expressed in &lt;i>Escherichia coli&lt;/i> and HEK Cells for Serological Detection of Antibodies in Response to SARS-CoV-2 Infections and mRNA-Based Vaccinations.</pubmed_title><pmcid>PMC9782079</pmcid><funding_grant_id>100523073</funding_grant_id><funding_grant_id>INST 268/387-1</funding_grant_id><pubmed_authors>Schwarze M</pubmed_authors><pubmed_authors>Scholz M</pubmed_authors><pubmed_authors>Gabert J</pubmed_authors><pubmed_authors>Borte S</pubmed_authors><pubmed_authors>Milkovska-Stamenova S</pubmed_authors><pubmed_authors>Grunewald T</pubmed_authors><pubmed_authors>Brakel A</pubmed_authors><pubmed_authors>Lakowa N</pubmed_authors><pubmed_authors>Luo J</pubmed_authors><pubmed_authors>Wolf J</pubmed_authors><pubmed_authors>Krizsan A</pubmed_authors><pubmed_authors>Lehmann C</pubmed_authors><pubmed_authors>Hoffmann R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evaluation of S- and M-Proteins Expressed in &lt;i>Escherichia coli&lt;/i> and HEK Cells for Serological Detection of Antibodies in Response to SARS-CoV-2 Infections and mRNA-Based Vaccinations.</name><description>This study investigated the IgG and IgA antibody response against recombinant S1 and receptor binding domains (RBD) of the spike (S-) protein and the membrane (M-) protein using a set of 115 serum samples collected from patients infected with SARS-CoV-2 in Germany before April 2021 using protein and peptide ELISA. As S1- and RBD-proteins expressed in &lt;i>Escherichia coli&lt;/i> provided poor sensitivities in ELISA, they were replaced by proteins expressed in HEK cells. The RBD-ELISA provided a sensitivity of 90.6% (N = 85) for samples collected from patients with confirmed SARS-CoV-2 infections more than 14 days after symptom onset or a positive PCR test. In population-based controls, the specificity was 97.9% (N = 94). In contrast, the sensitivities were only 41.2% and 72.6% for M- and N-prot</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-04-08T10:58:57.835Z</modification><creation>2024-11-15T17:28:13.086Z</creation></dates><accession>S-EPMC9782079</accession><cross_references><pubmed>36558849</pubmed><doi>10.3390/pathogens11121515</doi></cross_references></HashMap>