Analysis of formalin-fixed, paraffin-embedded (FFPE) tissue via proteomic techniques and misconceptions of antigen retrieval

被引:40
作者
O'Rourke, Matthew B. [1 ]
Padula, Matthew P. [1 ]
机构
[1] Univ Technol Sydney, Prote Core Facil, Cnr Harris & Thomas St, Ultimo, NSW 2007, Australia
关键词
proteomics; mass spectrometry; formaldehyde fixation; antigen retrieval; IMAGING MASS-SPECTROMETRY; PROTEIN EXTRACTION; SAMPLE PREPARATION; CANCER-TISSUE; SHOTGUN PROTEOMICS; FROZEN TISSUE; LC-MS/MS; IDENTIFICATION; SECTIONS; PEPTIDE;
D O I
10.2144/000114414
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Since emerging in the late 19th century, formaldehyde fixation has become a standard method for preservation of tissues from clinical samples. The advantage of formaldehyde fixation is that fixed tissues can be stored at room temperature for decades without concern for degradation. This has led to the generation of huge tissue banks containing thousands of clinically significant samples. Here we review techniques for proteomic analysis of formalin-fixed, paraffin-embedded (FFPE) tissue samples with a specific focus on the methods used to extract and break formaldehyde crosslinks. We also discuss an error-of-interpretation associated with the technique known as "antigen retrieval." We have discovered that this term has been mistakenly applied to two disparate molecular techniques; therefore, we argue that a terminology change is needed to ensure accurate reporting of experimental results. Finally, we suggest that more investigation is required to fully understand the process of formaldehyde fixation and its subsequent reversal.
引用
收藏
页码:229 / +
页数:8
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