AI Article Synopsis

  • FFPE tissue repositories are important for studying disease progression and treatment responses, but proteins in these samples are often modified by formaldehyde, making extraction and analysis difficult.
  • A new method using heat and high pressure (40,000 psi) significantly improves protein extraction from FFPE mouse liver tissues, achieving a 4-fold increase in efficiency and a 30-fold increase in nonredundant protein identification compared to extraction with heat alone.
  • This improved method allows researchers to obtain protein profiles from FFPE tissues that are comparable to those from fresh-frozen tissues, enhancing the reliability of proteomic studies.

Article Abstract

Formaldehyde-fixed, paraffin-embedded (FFPE) tissue repositories represent a valuable resource for the retrospective study of disease progression and response to therapy. However, the proteomic analysis of FFPE tissues has been hampered by formaldehyde-induced protein modifications, which reduce protein extraction efficiency and may lead to protein misidentification. Here, we demonstrate the use of heat augmented with high hydrostatic pressure (40,000 psi) as a novel method for the recovery of intact proteins from FFPE mouse liver. When FFPE mouse liver was extracted using heat and elevated pressure, there was a 4-fold increase in protein extraction efficiency, a 3-fold increase in the extraction of intact proteins, and up to a 30-fold increase in the number of nonredundant proteins identified by mass spectrometry, compared to matched tissue extracted with heat alone. More importantly, the number of nonredundant proteins identified in the FFPE tissue was nearly identical to that of matched fresh-frozen tissue.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320745PMC
http://dx.doi.org/10.1021/pr201005tDOI Listing

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