Systematic evaluation and optimization of protein extraction parameters in diagnostic FFPE specimens

被引:11
作者
Dressler, Franz F. [1 ,6 ,7 ,8 ]
Schoenfeld, Jana [1 ]
Revyakina, Olga [1 ]
Vogele, Daniel [2 ]
Kiefer, Selina [3 ]
Kirfel, Jutta [1 ]
Gemoll, Timo [4 ]
Perner, Sven [1 ,5 ]
机构
[1] Univ Med Ctr Schleswig Holstein, Inst Pathol, Luebeck Site, Ratzeburger Allee 160, D-23562 Lubeck, Germany
[2] Univ Freiburg, Ctr Biol Syst Anal, Core Facil Prote, Habsburgerstr 49, D-79104 Freiburg, Germany
[3] Univ Freiburg, Fac Med, Dept Pathol, Med Ctr, Freiburg, Germany
[4] Univ Med Ctr Schleswig Holstein, Sect Translat Surg Oncol & Biobanking, Dept Surg, Campus Luebeck,Ratzeburger Allee 160, D-23562 Lubeck, Germany
[5] Leibniz Lung Ctr, Res Ctr Borstel, Inst Pathol, Parkallee 1-40, D-23845 Borstel, Germany
[6] Charite Univ Med Berlin, Inst Pathol, Berlin, Germany
[7] Humboldt Univ, Freie Univ Berlin, Berlin, Germany
[8] Berlin Inst Hlth, Berlin, Germany
关键词
Protein extraction; Formalin-fixed paraffin-embedded tissue; Clinical proteomics; Antigen retrieval; Crosslinking reversal; Protein analysis; Biomarker; PARAFFIN-EMBEDDED TISSUE; SAMPLE PREPARATION TECHNIQUES; PROTEOMIC ANALYSIS; DEPARAFFINIZATION; QUANTIFICATION; IDENTIFICATION; METHODOLOGY; EXPRESSION; QUALITY; UTILITY;
D O I
10.1186/s12014-022-09346-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Objectives Formalin-fixed paraffin-embedded (FFPE) tissue is the standard material for diagnostic pathology but poses relevant hurdles to accurate protein extraction due to cross-linking and chemical alterations. While numerous extraction protocols and chemicals have been described, systematic comparative analyses are limited. Various parameters were thus investigated in their qualitative and quantitative effects on protein extraction (PE) efficacy. Special emphasis was put on preservation of membrane proteins (MP) as key subgroup of functionally relevant proteins. Methods Using the example of urothelial carcinoma, FFPE tissue sections were subjected to various deparaffinization, protein extraction and antigen retrieval protocols and buffers as well as different extraction techniques. Performance was measured by protein concentration and western blot analysis of cellular compartment markers as well as liquid chromatography-coupled mass spectrometry (LC-MS). Results Commercially available extraction buffers showed reduced extraction of MPs and came at considerably increased costs. On-slide extraction did not improve PE whereas several other preanalytical steps could be simplified. Systematic variation of temperature and exposure duration demonstrated a quantitatively relevant corridor of optimal antigen retrieval. Conclusions Preanalytical protein extraction can be optimized at various levels to improve unbiased protein extraction and to reduce time and costs.
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页数:13
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