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10.1039/d1an00893e

http://scihub22266oqcxt.onion/10.1039/d1an00893e
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34250530!ä!34250530

suck abstract from ncbi


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pmid34250530      Analyst 2021 ; 146 (15): 4905-4917
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  • Cross-validation of ELISA and a portable surface plasmon resonance instrument for IgG antibody serology with SARS-CoV-2 positive individuals #MMPMID34250530
  • Djaileb A; Hojjat Jodaylami M; Coutu J; Ricard P; Lamarre M; Rochet L; Cellier-Goetghebeur S; Macaulay D; Charron B; Lavallee E; Thibault V; Stevenson K; Forest S; Live LS; Abonnenc N; Guedon A; Quessy P; Lemay JF; Farnos O; Kamen A; Stuible M; Gervais C; Durocher Y; Cholette F; Mesa C; Kim J; Cayer MP; de Grandmont MJ; Brouard D; Trottier S; Boudreau D; Pelletier JN; Masson JF
  • Analyst 2021[Jul]; 146 (15): 4905-4917 PMID34250530show ga
  • We report on the development of surface plasmon resonance (SPR) sensors and matching ELISAs for the detection of nucleocapsid and spike antibodies specific against the novel coronavirus 2019 (SARS-CoV-2) in human serum, plasma and dried blood spots (DBS). When exposed to SARS-CoV-2 or a vaccine against SARS-CoV-2, the immune system responds by expressing antibodies at levels that can be detected and monitored to identify the fraction of the population potentially immunized against SARS-CoV-2 and support efforts to deploy a vaccine strategically. A SPR sensor coated with a peptide monolayer and functionalized with various sources of SARS-CoV-2 recombinant proteins expressed in different cell lines detected human anti-SARS-CoV-2 IgG antibodies in clinical samples. Nucleocapsid expressed in different cell lines did not significantly change the sensitivity of the assays, whereas the use of a CHO cell line to express spike ectodomain led to excellent performance. This bioassay was performed on a portable SPR instrument capable of measuring 4 biological samples within 30 minutes of sample/sensor contact and the chip could be regenerated at least 9 times. Multi-site validation was then performed with in-house and commercial ELISA, which revealed excellent cross-correlations with Pearson's coefficients exceeding 0.85 in all cases, for measurements in DBS and plasma. This strategy paves the way to point-of-care and rapid testing for antibodies in the context of viral infection and vaccine efficacy monitoring.
  • |*COVID-19[MESH]
  • |*SARS-CoV-2[MESH]
  • |Antibodies, Viral[MESH]
  • |COVID-19 Vaccines[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G[MESH]
  • |Sensitivity and Specificity[MESH]
  • |Spike Glycoprotein, Coronavirus[MESH]


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