Analysis of automatically generated peptide mass fingerprints of cellular proteins and antigens from Helicobacter pylori 26695 separated by two-dimensional electrophoresis

被引:20
作者
Krah, A
Schmidt, F
Becher, D
Schmid, M
Albrecht, D
Rack, A
Büttner, K
Jungblut, PR
机构
[1] Max Planck Infect Biol, Core Facil Prot Anal, D-10117 Berlin, Germany
[2] Max Planck Infect Biol, Dept Mol Biol, D-10117 Berlin, Germany
[3] Univ Greifswald, Inst Microbiol, D-17487 Greifswald, Germany
关键词
D O I
10.1074/mcp.M300077-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Helicobacter pylori is a causative agent of severe diseases of the gastric tract ranging from chronic gastritis to gastric cancer. Cellular proteins of H. pylori were separated by high resolution two-dimensional gel electrophoresis. A dataset of 384 spots was automatically picked, digested, spotted, and analyzed by matrix-assisted laser desorption ionization mass spectrometry peptide mass fingerprint in triple replicates. This procedure resulted in 960 evaluable mass spectra. Using a new version of our data analysis software MS-Screener we improved identification and tested reliability of automatically generated data by comparing with manually produced data. Antigenic proteins from H. pylori are candidates for vaccines and diagnostic tests. Previous immunoproteomics studies of our group revealed antigen candidates, and 24 of them were now closely analyzed using the MS-Screener software. Only in three spots minor components were found that may have influenced their antigenicities. These findings affirm the value of immunoproteomics as a hypothesis-free approach. Additionally, the protein species distribution of the known antigen GroEL was investigated, dimers of the protein alkyl hydroperoxide reductase were found, and the fragmentation of gamma-glutamyltranspeptidase was demonstrated.
引用
收藏
页码:1271 / 1283
页数:13
相关论文
共 30 条
[1]   Genomic-sequence comparison of two unrelated isolates of the human gastric pathogen Helicobacter pylori [J].
Alm, RA ;
Ling, LSL ;
Moir, DT ;
King, BL ;
Brown, ED ;
Doig, PC ;
Smith, DR ;
Noonan, B ;
Guild, BC ;
deJonge, BL ;
Carmel, G ;
Tummino, PJ ;
Caruso, A ;
Uria-Nickelsen, M ;
Mills, DM ;
Ives, C ;
Gibson, R ;
Merberg, D ;
Mills, SD ;
Jiang, Q ;
Taylor, DE ;
Vovis, GF ;
Trost, TJ .
NATURE, 1999, 397 (6715) :176-180
[2]   Proteome analysis of secreted proteins of the gastric pathogen Helicobacter pylori [J].
Bumann, D ;
Aksu, S ;
Wendland, M ;
Janek, K ;
Zimny-Arndt, U ;
Sabarth, N ;
Meyer, TF ;
Jungblut, PR .
INFECTION AND IMMUNITY, 2002, 70 (07) :3396-3403
[3]  
Bumann D, 2001, PROTEOMICS, V1, P473, DOI 10.1002/1615-9861(200104)1:4<473::AID-PROT473>3.3.CO
[4]  
2-7
[5]   Unmatched masses in peptide mass fingerprints caused by cross-contamination: An updated statistical result [J].
Ding, QX ;
Xiao, L ;
Xiong, SX ;
Jia, YF ;
Que, HP ;
Guo, YJ ;
Liu, SJ .
PROTEOMICS, 2003, 3 (07) :1313-1317
[6]   Analysis of changes in acute-phase plasma proteins in an acute inflammatory response and in rheumatoid arthritis using two-dimensional gel electrophoresis [J].
Doherty, NS ;
Littman, BH ;
Reilly, K ;
Swindell, AC ;
Buss, JM ;
Anderson, NL .
ELECTROPHORESIS, 1998, 19 (02) :355-363
[7]   Quantitative analysis of complex protein mixtures using isotope-coded affinity tags [J].
Gygi, SP ;
Rist, B ;
Gerber, SA ;
Turecek, F ;
Gelb, MH ;
Aebersold, R .
NATURE BIOTECHNOLOGY, 1999, 17 (10) :994-999
[8]  
Haas G, 2002, PROTEOMICS, V2, P313, DOI 10.1002/1615-9861(200203)2:3<313::AID-PROT313>3.0.CO
[9]  
2-7
[10]   Use of matrix clusters and trypsin autolysis fragments as mass calibrants in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry [J].
Harris, WA ;
Janecki, DJ ;
Reilly, JP .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (18) :1714-1722