Clinical biomarker discovery by SWATH-MS based label-free quantitative proteomics: impact of criteria for identification of differentiators and data normalization method

J Transl Med. 2019 May 31;17(1):184. doi: 10.1186/s12967-019-1937-9.

Abstract

Background: SWATH-MS has emerged as the strategy of choice for biomarker discovery due to the proteome coverage achieved in acquisition and provision to re-interrogate the data. However, in quantitative analysis using SWATH, each sample from the comparison group is run individually in mass spectrometer and the resulting inter-run variation may influence relative quantification and identification of biomarkers. Normalization of data to diminish this variation thereby becomes an essential step in SWATH data processing. In most reported studies, data normalization methods used are those provided in instrument-based data analysis software or those used for microarray data. This study, for the first time provides an experimental evidence for selection of normalization method optimal for biomarker identification.

Methods: The efficiency of 12 normalization methods to normalize SWATH-MS data was evaluated based on statistical criteria in 'Normalyzer'-a tool which provides comparative evaluation of normalization by different methods. Further, the suitability of normalized data for biomarker discovery was assessed by evaluating the clustering efficiency of differentiators, identified from the normalized data based on p-value, fold change and both, by hierarchical clustering in Genesis software v.1.8.1.

Results: Conventional statistical criteria identified VSN-G as the optimal method for normalization of SWATH data. However, differentiators identified from VSN-G normalized data failed to segregate test and control groups. We thus assessed data normalized by eleven other methods for their ability to yield differentiators which segregate the study groups. Datasets in our study demonstrated that differentiators identified based on p-value from data normalized with Loess-R stratified the study groups optimally.

Conclusion: This is the first report of experimentally tested strategy for SWATH-MS data processing with an emphasis on identification of clinically relevant biomarkers. Normalization of SWATH-MS data by Loess-R method and identification of differentiators based on p-value were found to be optimal for biomarker discovery in this study. The study also demonstrates the need to base the choice of normalization method on the application of the data.

Keywords: Fold change; LC–MS; Normalization; Proteomic; SWATH; p-value.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / analysis*
  • Case-Control Studies
  • Datasets as Topic
  • Diagnosis, Differential
  • Escherichia coli
  • Evaluation Studies as Topic
  • HeLa Cells
  • Humans
  • K562 Cells
  • Mass Spectrometry* / methods
  • Mass Spectrometry* / standards
  • Peptide Fragments / analysis
  • Peptide Fragments / chemistry
  • Proteome / analysis*
  • Proteome / standards
  • Proteomics* / methods
  • Proteomics* / standards
  • Reference Standards
  • Reference Values
  • Software
  • Staining and Labeling
  • Yeasts

Substances

  • Biomarkers
  • Peptide Fragments
  • Proteome