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10.1021/acscentsci.0c00742

http://scihub22266oqcxt.onion/10.1021/acscentsci.0c00742
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C7586461!7586461!33372199
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suck abstract from ncbi


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pmid33372199      ACS+Cent+Sci 2020 ; 6 (12): 2238-49
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  • SARS-CoV-2 Proteome Microarray for Mapping COVID-19 Antibody Interactions at Amino Acid Resolution #MMPMID33372199
  • Wang H; Wu X; Zhang X; Hou X; Liang T; Wang D; Teng F; Dai J; Duan H; Guo S; Li Y; Yu X
  • ACS Cent Sci 2020[Dec]; 6 (12): 2238-49 PMID33372199show ga
  • Comprehensive profiling of humoral antibody response to severe acute respiratory syndrome (SARS) coronavirus-2 (CoV-2) proteins is essential in understanding the host immunity and in developing diagnostic tests and vaccines. To address this concern, we developed a SARS-CoV-2 proteome peptide microarray to analyze antibody interactions at the amino acid resolution. With the array, we demonstrate the feasibility of employing SARS-CoV-1 antibodies to detect the SARS-CoV-2 nucleocapsid phosphoprotein. The first landscape of B-cell epitopes for SARS-CoV-2 IgM and IgG antibodies in the serum of 10 coronavirus disease of 2019 (COVID-19) patients with early infection is also constructed. With array data and structural analysis, a peptide epitope for neutralizing antibodies within the SARS-CoV-2 spike receptor-binding domain?s interaction interface with the angiotensin-converting enzyme 2 receptor was predicted. All the results demonstrate the utility of our microarray as a platform to determine the changes of antibody responses in COVID-19 patients and animal models as well as to identify potential targets for diagnosis and treatment.
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