| Literature DB >> 33950498 |
Kathrin E Witzke1,2, Frederik Großerueschkamp3, Klaus Gerwert3, Barbara Sitek4,5,6.
Abstract
A label-free approach based on a highly reproducible and stable workflow allows for quantitative proteome analysis . Due to advantages compared to labeling methods, the label-free approach has the potential to measure unlimited samples from clinical specimen monitoring and comparing thousands of proteins. The presented label-free workflow includes a new sample preparation technique depending on automatic annotation and tissue isolation via FTIR-guided laser microdissection, in-solution digestion, LC-MS/MS analyses, data evaluation by means of Proteome Discoverer and Progenesis software, and verification of differential proteins. We successfully applied this workflow in a proteomics study analyzing human cystitis and high-grade urothelial carcinoma tissue regarding the identification of a diagnostic tissue biomarker. The differential analysis of only 1 mm2 of isolated tissue cells led to 74 significantly differentially abundant proteins.Entities:
Keywords: AHNAK2; Bladder cancer; FTIR imaging; Label-free proteomics; Laser microdissection; Urothelial cell carcinoma (UCC)
Year: 2021 PMID: 33950498 DOI: 10.1007/978-1-0716-1024-4_20
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745