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10.3390/vaccines9010035

http://scihub22266oqcxt.onion/10.3390/vaccines9010035
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33440622!7827214!33440622
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suck abstract from ncbi


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pmid33440622      Vaccines+(Basel) 2021 ; 9 (1): ä
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  • SARS-CoV-2 Epitope Mapping on Microarrays Highlights Strong Immune-Response to N Protein Region #MMPMID33440622
  • Musico A; Frigerio R; Mussida A; Barzon L; Sinigaglia A; Riccetti S; Gobbi F; Piubelli C; Bergamaschi G; Chiari M; Gori A; Cretich M
  • Vaccines (Basel) 2021[Jan]; 9 (1): ä PMID33440622show ga
  • A workflow for rapid SARS-CoV-2 epitope discovery on peptide microarrays is herein reported. The process started with a proteome-wide screening of immunoreactivity based on the use of a high-density microarray followed by a refinement and validation phase on a restricted panel of probes using microarrays with tailored peptide immobilization through a click-based strategy. Progressively larger, independent cohorts of Covid-19 positive sera were tested in the refinement processes, leading to the identification of immunodominant regions on SARS-CoV-2 spike (S), nucleocapsid (N) protein and Orf1ab polyprotein. A summary study testing 50 serum samples highlighted an epitope of the N protein (region 155-71) providing good diagnostic performance in discriminating Covid-19 positive vs. healthy individuals. Using this epitope, 92% sensitivity and 100% specificity were reached for IgG detection in Covid-19 samples, and no cross-reactivity with common cold coronaviruses was detected. Likewise, IgM immunoreactivity in samples collected within the first month after symptoms onset showed discrimination ability. Overall, epitope 155-171 from N protein represents a promising candidate for further development and rapid implementation in serological tests.
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