4.5 Article

Comparative evaluation of two methods for LC-MS/MS proteomic analysis of formalin fixed and paraffin embedded tissues

Journal

JOURNAL OF PROTEOMICS
Volume 235, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jprot.2021.104117

Keywords

FFPE; Protein extraction; RapiGest; FASP; LC-MS/MS; Label-free data-independent acquisition

Funding

  1. National Institute of Mental Health
  2. Fogarty International Center [R01 MH098786]

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This study compared two different sample preparation methods for shotgun proteomic analysis of FFPE tissues and found that RapiGest identified more proteins, exhibited higher technical reproducibility, and showed greater similarity to fresh tissues compared to FASP. Therefore, RapiGest is recommended for biomarker and quantification studies due to its better performance in protein identification and preservation in FFPE tissues.
The proteomics of formalin-fixed, paraffin-embedded (FFPE) samples has advanced significantly during the last two decades, but there are many protocols and few studies comparing them directly. There is no consensus on the most effective protocol for shotgun proteomic analysis. We compared the in-solution digestion with RapiGest and Filter Aided Sample Preparation (FASP) of FFPE prostate tissues stored 7 years and mirroring fresh frozen samples, using two label-free data-independent LC-MS/MS acquisitions. RapiGest identified more proteins than FASP, with almost identical numbers of proteins from fresh and FFPE tissues and 69% overlap, good preservation of high-MW proteins, no bias regarding isoelectric point, and greater technical reproducibility. On the other hand, FASP yielded 20% fewer protein identifications in FFPE than in fresh tissue, with 64-69% overlap, depletion of proteins >70 kDa, lower efficiency in acidic and neutral range, and lower technical reproducibility. Both protocols showed highly similar subcellular compartments distribution, highly similar percentages of extracted unique peptides from FFPE and fresh tissues and high positive correlation between the absolute quantitation values of fresh and FFPE proteins. In conclusion, RapiGest extraction of FFPE tissues delivers a proteome that closely resembles the fresh frozen proteome and should be preferred over FASP in biomarker and quantification studies. Significance: Here we analyzed the performance of two sample preparation methods for shotgun proteomic analysis of FFPE tissues to give a comprehensive overview of the obtained proteomes and the resemblance to its matching fresh frozen counterparts. These findings give us better understanding towards competent proteomics analysis of FFPE tissues. It is hoped that it will encourage further assessments of available protocols before establishing the most effective protocol for shotgun proteomic FFPE tissue analysis.

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