| Download | - View final version: Production and characterization of a SARS-CoV-2 nucleocapsid protein reference material (PDF, 2.0 MiB)
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| DOI | Resolve DOI: https://doi.org/10.1021/acsmeasuresciau.2c00050 |
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| Author | Search for: Stocks, Bradley B.1ORCID identifier: https://orcid.org/0000-0002-7265-9344; Search for: Thibeault, Marie-Pier1; Search for: L’Abbé, Denis2; Search for: Stuible, Matthew2; Search for: Durocher, Yves2; Search for: Melanson, Jeremy E.1ORCID identifier: https://orcid.org/0000-0002-2290-0101 |
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| Affiliation | - National Research Council of Canada. Metrology Research Centre
- National Research Council of Canada. Human Health Therapeutics
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| Format | Text, Article |
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| Subject | COVID-19; SARS-CoV-2; nucleocapsid protein; reference materials; isotope dilution; materials; monomers; peptides; proteins |
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| Abstract | Rapid antigen tests have become a widely used COVID-19 diagnostic tool with demand accelerating in response to the highly contagious SARS-CoV-2 Omicron variant. Hundreds of such test kits are approved for use worldwide, predominantly reporting on the presence of the viral nucleocapsid (N) protein, yet the comparability among manufacturers remains unclear and the need for reference standards is recognized. To address this lack of standardization, the National Research Council Canada has developed a SARS-CoV-2 nucleocapsid protein reference material solution, NCAP-1. Reference value determination for N protein content was realized by amino acid analysis (AAA) via double isotope dilution liquid chromatography–tandem mass spectrometry (LC-ID-MS/MS) following acid hydrolysis of the protein, in conjunction with UV spectrophotometry based on tryptophan and tyrosine absorbance at 280 nm. The homogeneity of the material was established through spectrophotometric absorbance readings at 280 nm. The molar concentration of the N protein in NCAP-1 was 10.0 ± 1.9 μmol L⁻¹ (k = 2, 95% confidence interval). Reference mass concentration and mass fraction values were subsequently calculated using the protein molecular weight and density of the NCAP-1 solution. Changes to protein higher-order structure, probed by size-exclusion liquid chromatography (LC-SEC) with UV detection, were used to evaluate transportation and storage stabilities. LC-SEC revealed nearly 90% of the N protein in the material is present as a mixture of hexamers and tetramers. The remaining low molecular weight species (<30 kDa) were interrogated by top-down mass spectrometry and determined to be autolysis products homologous to those previously documented for N protein of the original SARS-CoV. |
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| Publication date | 2022-09-02 |
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| Publisher | American Chemical Society (ACS) |
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| Language | English |
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| Peer reviewed | Yes |
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| Export citation | Export as RIS |
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| Report a correction | Report a correction (opens in a new tab) |
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| Record identifier | 0ece07e7-e18e-4382-93cf-9919632550b0 |
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| Record created | 2023-01-05 |
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| Record modified | 2023-01-06 |
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