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Differential proteomic analysis of HT29 Cl.16E and intestinal epithelial cells by LC ESI/QTOF mass spectrometry

  • Paolo Nanni
  • , Laura Mezzanotte
  • , Giulia Roda
  • , Alessandra Caponi
  • , Fredrik Levander
  • , Peter James
  • , Aldo Roda*
  • *Corresponding author for this work
  • IRCCS Azienda Ospedaliero-Universitaria di Bologna
  • S. Orsola-Malpighi Hospital
  • Lund University
  • University of Bologna

Research output: Contribution to journalArticleAcademicpeer-review

24 Citations (Scopus)

Abstract

Intestinal epithelial cells (IECs) play a key role in Crohn's disease, a chronic inflammatory bowel disease which requires invasive examinations to be diagnosed. The comparison of the cellular protein expression profiles of Crohn's disease patients and healthy subjects is fundamental for the identification of proteins clinically relevant as new biomarkers or as drug targets. For this purpose a differential label-free nano-LC ESI/QTOF mass spectrometry (MS) approach combined with targeted MS/MS analysis has been developed and applied to isolated IECs. We report here a study of the protein variations in IECs from healthy subjects (H) and Crohn's disease patients (CD). The method was previously validated using HT29 Cl.16E cell line, normal or treated with interferon-γ as a model of inflammation. Subcellular fractions proteins were extracted from HT29 and IECs and for each fraction monodimensional gel-electrophoresis was performed and the proteins subjected to tryptic digestion. The resulting peptides were analysed by LC ESI/QTOF MS and the obtained chromatographic runs were aligned with msInspect software. The peptides differently expressed were statistically evaluated using the Proteios Software Environment (ProSE) and identified by LC ESI/QTOF MS/MS analysis and database search. The preliminary results obtained allowed the identification of many proteins involved in the inflammation processes.

Original languageEnglish
Pages (from-to)865-873
Number of pages9
JournalJournal of Proteomics
Volume72
Issue number5
DOIs
Publication statusPublished - 21 Jul 2009
Externally publishedYes

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