| Literature DB >> 35397901 |
Kenneth Weke1, Sachin Kote2, Jakub Faktor1, Sofian Al Shboul3, Naomi Uwugiaren1, Paul M Brennan4, David R Goodlett5, Ted R Hupp6, Irena Dapic7.
Abstract
Developments in quantitative proteomics and data-independent acquisition (DIA) methodology is enabling quantification of proteins in biological samples. Currently, there are a few reports on DIA mass spectrometry (MS) approaches for proteome analysis of formalin-fixed paraffin-embedded (FFPE) tissues. Therefore, to facilitate detection and quantification of immune- and glioblastoma (GBM)-relevant proteins from FFPE patient materials, we established a simple and precise DIA-MS workflow. We first evaluated different lysis buffers for their efficiency in protein extractions from FFPE GBM tissues. Our results showed that more than 1700 proteins were detected and over 1400 proteins were quantified from GBM FFPE tissue microdissections. GBM-relevant proteins (e.g., GFAP, FN1, VIM, and MBP) were quantified with high precision (median coefficient of variation <12%). In addition, immune-related proteins (e.g., ILF2, MIF, and CD38) were consistently detected and quantified. The strategy holds great potential for routinizing protein quantification in FFPE tissue samples.Entities:
Keywords: Data-independent acquisition; Formalin-fixed paraffin-embedded; Glioblastoma; Mass spectrometry; Quantitative proteomics
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Year: 2022 PMID: 35397901 DOI: 10.1016/j.aca.2022.339695
Source DB: PubMed Journal: Anal Chim Acta ISSN: 0003-2670 Impact factor: 6.558