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• W4296030298 startingPage "2443" @default.
• W4296030298 abstract "The SARS-CoV-2 omicron variant presented significant challenges to the global effort to counter the pandemic. SARS-CoV-2 is predicted to remain prevalent for the foreseeable future, making the ability to identify SARS-CoV-2 variants imperative in understanding and controlling the pandemic. The predominant variant discovery method, genome sequencing, is time-consuming, insensitive, and expensive. Ultraperformance liquid chromatography–mass spectrometry (UPLC–MS) offers an exciting alternative detection modality provided that variant-containing peptide markers are sufficiently detectable from their tandem mass spectra (MS/MS). We have synthesized model tryptic peptides of SARS-CoV-2 variants alpha, beta, gamma, delta, and omicron and evaluated their signal intensity, HCD spectra, and reverse phase retention time. Detection limits of 781, 781, 65, and 65 amol are obtained for the molecular ions of the proteotypic peptides, beta (QIAPGQTGNIADYNYK), gamma (TQLPSAYTNSFTR), delta (VGGNYNYR), and omicron (TLVKQLSSK), from neat solutions. These detection limits are on par with the detection limits of a previously reported proteotypic peptide from the SARS-CoV-2 spike protein, HTPINLVR. This study demonstrates the potential to differentiate SARS-CoV-2 variants through their proteotypic peptides with an approach that is broadly applicable across a wide range of pathogens." @default.
• W4296030298 created "2022-09-17" @default.
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• W4296030298 date "2022-09-15" @default.
• W4296030298 modified "2023-10-09" @default.
• W4296030298 title "Evaluation of Variant-Specific Peptides for Detection of SARS-CoV-2 Variants of Concern" @default.
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• W4296030298 doi "https://doi.org/10.1021/acs.jproteome.2c00325" @default.
• W4296030298 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36108102" @default.
• W4296030298 hasPublicationYear "2022" @default.
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