Robust optimization of SWATH-MS workflow for human blood serum proteome analysis using a quality by design approach

被引:5
|
作者
Serrano-Blesa, Edith [1 ,2 ]
Porter, Andrew [3 ]
Lendrem, Dennis W. [1 ,2 ]
Pitzalis, Costantino [4 ]
Barton, Anne [5 ]
Treumann, Achim [3 ]
Isaacs, John D. [1 ,2 ,6 ]
机构
[1] Newcastle Univ, Newcastle Biomed Res Ctr, Natl Inst Hlth Res, Newcastle Upon Tyne, Tyne & Wear, England
[2] Newcastle Univ, Translat & Clin Res Inst, Newcastle Upon Tyne, Tyne & Wear, England
[3] Newcastle Univ, Prot & Proteome Facil, Newcastle Upon Tyne, Tyne & Wear, England
[4] Queen Mary Univ London, Ctr Expt Med & Rheumatol, London, England
[5] Univ Manchester, Manchester Acad Hlth Sci Ctr, Versus Arthrit Ctr Genet & Genom, Fac Biol Med & Hlth,Ctr Musculoskeletal Res, Manchester, Lancs, England
[6] Newcastle upon Tyne NHS Fdn Trust, Freeman Hosp, Musculoskeletal Unit, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
SWATH-MS; Proteomic quantification; Design of experiments; Quality by design; Screening; Optimization; Robustness; BIOMARKER DISCOVERY; ACQUISITION; QUANTIFICATION;
D O I
10.1186/s12014-021-09323-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background It is not enough to optimize proteomics assays. It is critical those assays are robust to operating conditions. Without robust assays, proteomic biomarkers are unlikely to translate readily into the clinic. This study outlines a structured approach to the identification of a robust operating window for proteomics assays and applies that method to Sequential Window Acquisition of all Theoretical Spectra Mass Spectroscopy (SWATH-MS). Methods We used a sequential quality by design approach exploiting a fractional screening design to first identify critical SWATH-MS parameters, then using response surface methods to identify a robust operating window with good reproducibility, before validating those settings in a separate validation study. Results The screening experiment identified two critical SWATH-MS parameters. We modelled the number of proteins and reproducibility as a function of those parameters identifying an operating window permitting robust maximization of the number of proteins quantified in human serum. In a separate validation study, these settings were shown to give good proteome-wide coverage and high quantification reproducibility. Conclusions Using design of experiments permits identification of a robust operating window for SWATH-MS. The method gives a good understanding of proteomics assays and greater data-driven confidence in SWATH-MS performance.
引用
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页数:9
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