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10.1038/s41598-021-83730-y

http://scihub22266oqcxt.onion/10.1038/s41598-021-83730-y
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33619344!7900118!33619344
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suck abstract from ncbi


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pmid33619344      Sci+Rep 2021 ; 11 (1): 4290
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  • In silico detection of SARS-CoV-2 specific B-cell epitopes and validation in ELISA for serological diagnosis of COVID-19 #MMPMID33619344
  • Phan IQ; Subramanian S; Kim D; Murphy M; Pettie D; Carter L; Anishchenko I; Barrett LK; Craig J; Tillery L; Shek R; Harrington WE; Koelle DM; Wald A; Veesler D; King N; Boonyaratanakornkit J; Isoherranen N; Greninger AL; Jerome KR; Chu H; Staker B; Stewart L; Myler PJ; Van Voorhis WC
  • Sci Rep 2021[Feb]; 11 (1): 4290 PMID33619344show ga
  • Rapid generation of diagnostics is paramount to understand epidemiology and to control the spread of emerging infectious diseases such as COVID-19. Computational methods to predict serodiagnostic epitopes that are specific for the pathogen could help accelerate the development of new diagnostics. A systematic survey of 27 SARS-CoV-2 proteins was conducted to assess whether existing B-cell epitope prediction methods, combined with comprehensive mining of sequence databases and structural data, could predict whether a particular protein would be suitable for serodiagnosis. Nine of the predictions were validated with recombinant SARS-CoV-2 proteins in the ELISA format using plasma and sera from patients with SARS-CoV-2 infection, and a further 11 predictions were compared to the recent literature. Results appeared to be in agreement with 12 of the predictions, in disagreement with 3, while a further 5 were deemed inconclusive. We showed that two of our top five candidates, the N-terminal fragment of the nucleoprotein and the receptor-binding domain of the spike protein, have the highest sensitivity and specificity and signal-to-noise ratio for detecting COVID-19 sera/plasma by ELISA. Mixing the two antigens together for coating ELISA plates led to a sensitivity of 94% (N = 80 samples from persons with RT-PCR confirmed SARS-CoV-2 infection), and a specificity of 97.2% (N = 106 control samples).
  • |COVID-19/*diagnosis/*immunology[MESH]
  • |Enzyme-Linked Immunosorbent Assay/*methods[MESH]
  • |Epitopes, B-Lymphocyte/*immunology[MESH]
  • |Humans[MESH]
  • |Real-Time Polymerase Chain Reaction[MESH]
  • |SARS-CoV-2/immunology/*pathogenicity[MESH]


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