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- W4200467922 abstract "Abstract Accurate relative quantification is critical in proteomic studies. The incorporation of stable isotope 15 N to plant-expressed proteins in vivo is a powerful tool for accurate quantification with a major advantage of reducing preparative and analytical variabilities. However, 15 N labeling quantification has several challenges. Less identifications are often observed in the heavy labeled samples because of incomplete labeling, resulting in missing values in reciprocal labeling experiments. Inaccurate quantification can happen when there is contamination from co-eluting peptides or chemical noise in the MS 1 survey scan. These drawbacks in quantification can be more pronounced in less abundant but biologically interesting proteins, which often have very few identified peptides. Here we demonstrate the application of parallel reaction monitoring (PRM) to 15 N labeled samples on a high resolution, high mass accuracy Orbitrap mass spectrometer to achieve reliable quantification even of low abundance proteins in samples." @default.
- W4200467922 created "2021-12-31" @default.
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- W4200467922 date "2021-12-03" @default.
- W4200467922 modified "2023-10-16" @default.
- W4200467922 title "Application of Parallel Reaction Monitoring in <sup>15</sup>N labeled Samples for Quantification" @default.
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- W4200467922 doi "https://doi.org/10.1101/2021.12.01.470846" @default.
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