Difference gel electrophoresis identifies differentially expressed proteins in endoscopically collected pancreatic fluid

被引:5
作者
Paulo, Joao A. [1 ,2 ,3 ,4 ]
Lee, Linda S. [1 ,2 ]
Banks, Peter A. [1 ,2 ]
Steen, Hanno [3 ,4 ]
Conwell, Darwin L. [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Ctr Pancreat Dis, Div Gastroenterol Hepatol & Endoscopy, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[3] Childrens Hosp Boston, Dept Pathol, Boston, MA USA
[4] Childrens Hosp Boston, Prote Ctr, Boston, MA USA
关键词
Biomarkers; Pancreas; Pancreatic function test; Pancreatic juice; SYNTHETIC PORCINE SECRETIN; PROTEOMIC ANALYSIS; PROTEASE INHIBITORS; MASS-SPECTROMETRY; STELLATE CELLS; RISK-FACTORS; DIAGNOSIS; COMPLICATIONS; CONSEQUENCES; ENDOPLASMIN;
D O I
10.1002/elps.201100203
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Alterations in the pancreatic fluid proteome of individuals with chronic pancreatitis (CP) may offer insights into the development and progression of the disease. The endoscopic pancreatic function test (ePFT) can safely collect large volumes of pancreatic fluid that are potentially amenable to proteomic analyses using difference gel electrophoresis (DIGE) coupled with liquid chromatography-tandem mass spectrometry (LC-MS/MS). Pancreatic fluid was collected endoscopically using the ePFT method following secretin stimulation from three individuals with severe CP and three chronic abdominal pain (CAP) controls. The fluid was processed to minimize protein degradation and the protein profiles of each cohort, as determined by DIGE and LC-MS/MS, were compared. This DIGE-LC-MS/MS analysis reveals proteins that are differentially expressed in CP compared with CAP controls. Proteins with higher abundance in pancreatic fluid from CP individuals include: actin, desmoplankin, alpha-1-antitrypsin, SNC73, and serotransferrin. Those of relatively lower abundance include carboxypeptidase B, lipase, alpha-1-antichymotrypsin, alpha-2-macroglobulin, actin-related protein (Arp2/3) subunit 4, glyceraldehyde-3-phosphate dehydrogenase, and protein disulfide isomerase. Endoscopic collection (ePFT) in tandem with DIGE-LC-MS/MS is a suitable approach for pancreatic fluid proteome analysis; however, further optimization of our protocol, as outlined herein, may improve proteome coverage in future analyses.
引用
收藏
页码:1939 / 1951
页数:13
相关论文
共 67 条
[1]   Chronic Pancreatitis: Recent Advances and Ongoing Challenges - In brief [J].
Ahmad, SA ;
Wray, CJ ;
Rilo, HR ;
Choe, KA ;
Gelrud, A ;
Howington, J ;
Lowy, AM ;
Matthews, JB .
CURRENT PROBLEMS IN SURGERY, 2006, 43 (03) :127-238
[2]   Incidence rates of post-ERCP complications: A systematic survey of prospective studies [J].
Andriulli, Angelo ;
Loperfido, Silvano ;
Napolitano, Grazia ;
Niro, Grazia ;
Valvano, Maria Rosa ;
Spirito, Fulvio ;
Pilotto, Alberto ;
Forlano, Rosario .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 (08) :1781-1788
[3]   The universal protein resource (UniProt) [J].
Bairoch, A ;
Apweiler, R ;
Wu, CH ;
Barker, WC ;
Boeckmann, B ;
Ferro, S ;
Gasteiger, E ;
Huang, HZ ;
Lopez, R ;
Magrane, M ;
Martin, MJ ;
Natale, DA ;
O'Donovan, C ;
Redaschi, N ;
Yeh, LSL .
NUCLEIC ACIDS RESEARCH, 2005, 33 :D154-D159
[4]   Comparison of different depletion strategies for improved resolution in proteomic analysis of human serum samples [J].
Björhall, K ;
Miliotis, T ;
Davidsson, P .
PROTEOMICS, 2005, 5 (01) :307-317
[5]   Breaking the connection: Displacement of the desmosomal plaque protein desmoplakin from cell-cell interfaces disrupts anchorage of intermediate filament bundles and alters intercellular junction assembly [J].
Bornslaeger, EA ;
Corcoran, CM ;
Stappenbeck, TS ;
Green, KJ .
JOURNAL OF CELL BIOLOGY, 1996, 134 (04) :985-1001
[6]   GRP94 (endoplasmin) co-purifies with and is phosphorylated by Golgi apparatus casein kinase [J].
Brunati, AM ;
Contri, A ;
Muenchbach, M ;
James, P ;
Marin, O ;
Pinna, LA .
FEBS LETTERS, 2000, 471 (2-3) :151-155
[7]   The need for guidelines in publication of peptide and protein identification data - Working group on publication guidelines for peptide and protein identification data [J].
Carr, S ;
Aebersold, R ;
Baldwin, M ;
Burlingame, A ;
Clauser, K ;
Nesvizhskii, A .
MOLECULAR & CELLULAR PROTEOMICS, 2004, 3 (06) :531-533
[8]   Quantitative proteomics analysis reveals that proteins differentially expressed in chronic pancreatitis are also frequently involved in pancreatic cancer [J].
Chen, Ru ;
Brentnall, Teresa A. ;
Pan, Sheng ;
Cooke, Kelly ;
Moyes, Kara White ;
Lane, Zhaoli ;
Crispin, David A. ;
Goodlett, David R. ;
Aebersold, Ruedi ;
Bronner, Mary P. .
MOLECULAR & CELLULAR PROTEOMICS, 2007, 6 (08) :1331-1342
[9]   Quantitative proteomic profiling of pancreatic cancer juice [J].
Chen, Ru ;
Sheng, Pan ;
Yi, Eugene C. ;
Donohoe, Samuel ;
Bronner, Mary P. ;
Potter, John D. ;
Goodlett, David R. ;
Aebersold, Ruedi ;
Brentnall, Teresa A. .
PROTEOMICS, 2006, 6 (13) :3871-3879
[10]   Risk factors for post-ERCP pancreatitis: A prospective multicenter study [J].
Cheng, CL ;
Sherman, S ;
Watkins, JL ;
Barnett, J ;
Freeman, M ;
Geenen, J ;
Ryan, M ;
Parker, H ;
Frakes, JT ;
Fogel, EL ;
Silverman, WB ;
Dua, KS ;
Aliperti, G ;
Yakshe, P ;
Uzer, M ;
Jones, W ;
Goff, J ;
Lazzell-Pannell, L ;
Rashdan, A ;
Temkit, M ;
Lehman, GA .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (01) :139-147