Bioinformatics strategies for proteomic profiling

被引:53
作者
White, CN [1 ]
Chan, DW [1 ]
Zhang, Z [1 ]
机构
[1] Johns Hopkins Med Inst, Ctr Biomarker Discovery, Dept Pathol, Baltimore, MD 21231 USA
关键词
bioinformatics; proteomic profiling; mass spectrometry; SELDI; quality control;
D O I
10.1016/j.clinbiochem.2004.05.004
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Clinical proteomics is an emerging field that involves the analysis of protein expression profiles of clinical samples for de novo discovery of disease-associated biomarkers and for gaining insight into the biology of disease processes. Mass spectrometry represents an important set of technologies for protein expression measurement. Among them, surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI TOF-MS), because of its high throughput and on-chip sample processing capability, has become a popular tool for clinical proteomics. Bioinformatics plays a critical role in the analysis of SELDI data, and therefore, it is important to understand the issues associated with the analysis of clinical proteomic data. In this review, we discuss such issues and the bioinformatics strategies used for proteomic profiling. (C) 2004 The Canadian Society of Clinical Chemists. All rights reserved.
引用
收藏
页码:636 / 641
页数:6
相关论文
共 35 条
[1]   A post-genomic challenge: learning to read patterns of protein synthesis [J].
Abbott, A .
NATURE, 1999, 402 (6763) :715-720
[2]   HIGH-RESOLUTION 2-DIMENSIONAL ELECTROPHORESIS OF HUMAN-PLASMA PROTEINS [J].
ANDERSON, L ;
ANDERSON, NG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5421-5425
[3]   Characterization of renal allograft rejection by urinary proteomic analysis [J].
Clarke, W ;
Silverman, BC ;
Zhang, Z ;
Chan, DW ;
Klein, AS ;
Molmenti, EP .
ANNALS OF SURGERY, 2003, 237 (05) :660-664
[4]   THE RISK OF DETERMINING RISK WITH MULTIVARIABLE MODELS [J].
CONCATO, J ;
FEINSTEIN, AR ;
HOLFORD, TR .
ANNALS OF INTERNAL MEDICINE, 1993, 118 (03) :201-210
[5]   SAMPLE-SIZE FOR TESTING DIFFERENCES IN PROPORTIONS FOR THE PAIRED-SAMPLE DESIGN [J].
CONNOR, RJ .
BIOMETRICS, 1987, 43 (01) :207-211
[6]   Quality control and peak finding for proteomics data collected from nipple aspirate fluid by surface-enhanced laser desorption and ionization [J].
Coombes, KR ;
Fritsche, HA ;
Clarke, C ;
Chen, JN ;
Baggerly, KA ;
Morris, JS ;
Xiao, LC ;
Hung, MC ;
Kuerer, HM .
CLINICAL CHEMISTRY, 2003, 49 (10) :1615-1623
[7]   Prostate carcinoma tissue proteomics for biomarker discovery [J].
Deng, YX ;
Xu, Y ;
Ye, B ;
Lei, JY ;
Weinstein, MH ;
O'Leary, MP ;
Richie, JP ;
Mok, SC ;
Liu, BCS .
CANCER, 2003, 98 (12) :2576-2582
[8]   Point - Proteomic patterns in biological fluids: Do they represent the future of cancer diagnostics? [J].
Diamandis, EP .
CLINICAL CHEMISTRY, 2003, 49 (08) :1272-1275
[9]   1977 RIETZ LECTURE - BOOTSTRAP METHODS - ANOTHER LOOK AT THE JACKKNIFE [J].
EFRON, B .
ANNALS OF STATISTICS, 1979, 7 (01) :1-26
[10]  
Fukanaga K., 1990, Introduction to statistical pattern recognition, V2