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Updated: Aug 23, 2026

Selected Reaction Monitoring Mass Spectrometry for Absolute Protein Quantification
Published on: August 17, 2015
Quantifying reproducibility for differential proteomics: noise analysis for protein liquid chromatography-mass
Markus Anderle1, Sushmita Roy, Hua Lin
1SurroMed, Inc., 1430 O'Brien Drive, Menlo Park, CA 94025, USA. manderle@surromed.com <manderle@surromed.com>
Summary:
Using replicated human serum samples, we applied an error model for proteomic differential expression profiling for a high-resolution liquid chromatography-mass spectrometry (LC-MS) platform. The detailed noise analysis presented here uses an experimental design that separates variance caused by sample preparation from variance due to analytical equipment. An analytic approach based on a two-component error model was applied, and in combination with an existing data driven technique that utilizes local sample averaging, we characterized and quantified the noise variance as a function of mean peak intensity. The results indicate that for processed LC-MS data a constant coefficient of variation is dominant for high intensities, whereas a model for low intensities explains Poisson-like variations. This result leads to a quadratic variance model which is used for the estimation of sample preparation noise present in LC-MS data.
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