Frontiers in Pharmacology (Jun 2018)

Discovery of the Consistently Well-Performed Analysis Chain for SWATH-MS Based Pharmacoproteomic Quantification

  • Jianbo Fu,
  • Jing Tang,
  • Jing Tang,
  • Yunxia Wang,
  • Xuejiao Cui,
  • Xuejiao Cui,
  • Qingxia Yang,
  • Qingxia Yang,
  • Jiajun Hong,
  • Xiaoxu Li,
  • Xiaoxu Li,
  • Shuang Li,
  • Shuang Li,
  • Yuzong Chen,
  • Weiwei Xue,
  • Feng Zhu,
  • Feng Zhu

DOI
https://doi.org/10.3389/fphar.2018.00681
Journal volume & issue
Vol. 9

Abstract

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Sequential windowed acquisition of all theoretical fragment ion mass spectra (SWATH-MS) has emerged as one of the most popular techniques for label-free proteome quantification in current pharmacoproteomic research. It provides more comprehensive detection and more accurate quantitation of proteins comparing with the traditional techniques. The performance of SWATH-MS is highly susceptible to the selection of processing method. Till now, ≥27 methods (transformation, normalization, and missing-value imputation) are sequentially applied to construct numerous analysis chains for SWATH-MS, but it is still not clear which analysis chain gives the optimal quantification performance. Herein, the performances of 560 analysis chains for quantifying pharmacoproteomic data were comprehensively assessed. Firstly, the most complete set of the publicly available SWATH-MS based pharmacoproteomic data were collected by comprehensive literature review. Secondly, substantial variations among the performances of various analysis chains were observed, and the consistently well-performed analysis chains (CWPACs) across various datasets were for the first time generalized. Finally, the log and power transformations sequentially followed by the total ion current normalization were discovered as one of the best performed analysis chains for the quantification of SWATH-MS based pharmacoproteomic data. In sum, the CWPACs identified here provided important guidance to the quantification of proteomic data and could therefore facilitate the cutting-edge research in any pharmacoproteomic studies requiring SWATH-MS technique.

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