4.7 Article

Characterization of a SARS-CoV-2 spike protein reference material

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 414, Issue 12, Pages 3561-3569

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-022-04000-y

Keywords

COVID-19; SARS-CoV-2; Spike protein; Reference materials; Isotope dilution

Funding

  1. NRC Pandemic Response Challenge Program

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The development of diagnostic testing capability in response to COVID-19 has made significant progress, but the lack of standardization has resulted in unreliable test results. To address this challenge, the National Research Council Canada has prepared a SARS-CoV-2 spike protein reference material to assist the research community. The material was characterized using various analytical techniques, including amino acid analysis and spectrophotometry, and its stability and concentration were determined.
Development of diagnostic testing capability has advanced with unprecedented pace in response to the COVID-19 pandemic. An undesirable effect of such speed is a lack of standardization, often leading to unreliable test results. To assist the research community surmount this challenge, the National Research Council Canada has prepared a SARS-CoV-2 spike protein reference material, SMT1-1, as a buffered solution. Value assignment was achieved by amino acid analysis (AAA) by double isotope dilution liquid chromatography-tandem mass spectrometry (LC-ID-MS/MS) following acid hydrolysis of the protein, in combination with ultraviolet-visible spectrophotometry (UV-Vis) based on tryptophan and tyrosine absorbance at 280 nm. Homogeneity of the material was established through spectrophotometric absorbance readings at 280 nm. Transportation and long-term storage stabilities were assessed by monitoring relative changes in oligomeric state by size-exclusion liquid chromatography (LC-SEC) with UV detection. The molar concentration of the spike protein in SMT1-1 was 5.68 +/- 0.22 mu mol L-1 (k = 2, 95% CI), with the native trimeric form accounting for similar to 94% of the relative abundance. Reference mass concentration and mass fraction values were calculated using the protein molecular weight and density of the SMT1-1 solution. The spike protein is highly glycosylated which leads to analyte ambiguity when reporting the more commonly used mass concentration. After glycoprotein molar mass determination by LC-SEC with multi-angle light scattering detection, we thus reported mass concentration values for both the protein-only portion and intact glycoprotein as 0.813 +/- 0.030 and 1.050 +/- 0.068 mg mL(-1) (k = 2), respectively.

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