Characterization of Glycoproteins in Pancreatic Cyst Fluid Using a High-Performance Multiple Lectin Affinity Chromatography Platform

• Published in: Journal of proteome research Vol. 13; no. 1; pp. 289 - 299
• Main Authors: Gbormittah, Francisca Owusu, Haab, Brian B, Partyka, Katie, Garcia-Ott, Carolina, Hancapie, Marina, Hancock, William S
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 03.01.2014
• Subjects: Chromatography, Affinity - methods; Electrophoresis, Polyacrylamide Gel; Glycoproteins - metabolism; Humans; Lectins - metabolism; Mass Spectrometry - methods; Pancreatic Cyst - metabolism; pancreatic cancer; glycoproteins; biomarker discovery; pancreatic cyst fluid; mucinous cyst; nonmucinous cyst
• ISSN: 1535-3893; 1535-3907
• DOI: 10.1021/pr400813u

Currently, pancreatic cancer is the fourth cause of cancer death. In 2013, it is estimated that ∼38 460 people will die of pancreatic cancer. Early detection of malignant cyst (pancreatic cancer precursor) is necessary to help prevent late diagnosis of the tumor. In this study, we characterized glycoproteins and nonglycoproteins on pooled mucinous (n = 10) and nonmucinous (n = 10) pancreatic cyst fluid to identify “proteins of interest” to differentiate between mucinous cyst from nonmucinous cyst and investigate these proteins as potential biomarker targets. An automated multilectin affinity chromatography (M-LAC) platform was utilized for glycoprotein enrichment followed by nano-LC–MS/MS analysis. Spectral count quantitation allowed for the identification of proteins with significant differential levels in mucinous cysts from nonmucinous cysts of which one protein (periostin) was confirmed via immunoblotting. To exhaustively evaluate differentially expressed proteins, we used a number of proteomic tools including gene ontology classification, pathway and network analysis, Novoseek data mining, and chromosome gene mapping. Utilization of complementary proteomic tools revealed that several of the proteins such as mucin 6 (MUC6), bile salt-activated lipase (CEL), and pyruvate kinase lysozyme M1/M2 with significant differential expression have strong association with pancreatic cancer. Furthermore, chromosome gene mapping demonstrated coexpressions and colocalization of some proteins of interest including 14-3-3 protein epsilon (YWHAE), pigment epithelium derived factor (SERPINF1), and oncogene p53.