2D differential in-gel electrophoresis for the identification of esophageal scans cell cancer-specific protein markers.

G. Zhou*, Hongmei Li, Dianne DeCamp, She Chen, Hongjun Shu, Y. Gong, Michael Flaig, John W. Gillespie, Nan Hu, Philip R. Taylor, Michael R. Emmert-Buck, Lance A. Liotta, Emanuel F. Petricoin, Yingming Zhao

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

353 Scopus citations

Abstract

The reproducibility of conventional two-dimensional (2D) gel electrophoresis can be improved using differential in-gel electrophoresis (DIGE), a new emerging technology for proteomic analysis. In DIGE, two pools of proteins are labeled with 1-(5-carboxypentyl)-1'-propylindocarbocyanine halide (Cy3) N-hydroxy-succinimidyl ester and 1-(5-carboxypentyl)-1'-methylindodi-carbocyanine halide (Cy5) N-hydroxysuccinimidyl ester fluorescent dyes, respectively. The labeled proteins are mixed and separated in the same 2D gel. 2D DIGE was applied to quantify the differences in protein expression between laser capture microdissection-procured esophageal carcinoma cells and normal epithelial cells and to define cancer-specific and normal-specific protein markers. Analysis of the 2D images from protein lysates of approximately 250,000 cancer cells and normal cells identified 1038 protein spots in cancer cell lysates and 1088 protein spots in normal cell lysates. Of the detected proteins, 58 spots were up-regulated by >3-fold and 107 were down-regulated by >3-fold in cancer cells. In addition to previously identified down-regulated protein annexin I, tumor rejection antigen (gp96) was found up-regulated in esophageal squamous cell cancer. Global quantification of protein expression between laser capture-microdissected patient-matched cancer cells and normal cells using 2D DIGE in combination with mass spectrometry is a powerful tool for the molecular characterization of cancer progression and identification of cancer-specific protein markers.

Original languageEnglish
Pages (from-to)117-124
Number of pages8
JournalMolecular and Cellular Proteomics
Volume1
Issue number2
DOIs
StatePublished - Feb 2002
Externally publishedYes

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