Analyzing alkaline proteins in human colon crypt proteome

被引:20
作者
Li, XM
Patel, BB
Blagoi, EL
Patterson, MD
Seehozer, SH
Zhang, T
Damle, S
Gao, ZQ
Boman, B
Yeung, AT
机构
[1] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[2] Thomas Jefferson Univ, Dept Med, Philadelphia, PA 19107 USA
关键词
2D-electrophoresis; alkaline protein; colon crypt; colorectal cancer; proteomics;
D O I
10.1021/pr049942j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Normal human colon crypt protein extract was resolved by two-dimensional gel electrophoresis using pH 6-11 immobilized pH gradient strips in the first dimension. The optimized isoelectric focusing protocol includes cup-loading sample application at the anode and 1.2% hydroxyethyl disulfide (DeStreak), 15% 2-propanol and 5% glycerol in the rehydration buffer. Spots were well resolved across the entire pH range up to 11. A total of 311 protein spots were identified by mass spectrometry and peptide mass mapping. After combining isoforms, 231 nonredundant proteins were grouped into 16 categories according to their subcellular locations, and 17 categories according to their physiological functions. Histone proteins, ribosomal proteins and mitochondrial proteins were among the well-resolved highest p/ proteins. Application of this protocol to the analysis of normal and neoplastic colon crypts will contribute to the proteomic study of colorectal tumorigenesis since a significant portion of the human proteins is in basic pH range.
引用
收藏
页码:821 / 833
页数:13
相关论文
共 40 条
[31]   APC mutations in sporadic colorectal tumors:: A mutational "hotspot" and interdependence of the "two hits" [J].
Rowan, AJ ;
Lamlum, H ;
Ilyas, M ;
Wheeler, J ;
Straub, J ;
Papadopoulou, A ;
Bicknell, D ;
Bodmer, WF ;
Tomlinson, IPM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3352-3357
[32]  
Seike M, 2003, CANCER RES, V63, P4641
[33]  
Stulík J, 1999, ELECTROPHORESIS, V20, P3638, DOI 10.1002/(SICI)1522-2683(19991201)20:18<3638::AID-ELPS3638>3.0.CO
[34]  
2-W
[35]  
TRACY RP, 1982, CLIN CHEM, V28, P915
[36]   The sequence of the human genome [J].
Venter, JC ;
Adams, MD ;
Myers, EW ;
Li, PW ;
Mural, RJ ;
Sutton, GG ;
Smith, HO ;
Yandell, M ;
Evans, CA ;
Holt, RA ;
Gocayne, JD ;
Amanatides, P ;
Ballew, RM ;
Huson, DH ;
Wortman, JR ;
Zhang, Q ;
Kodira, CD ;
Zheng, XQH ;
Chen, L ;
Skupski, M ;
Subramanian, G ;
Thomas, PD ;
Zhang, JH ;
Miklos, GLG ;
Nelson, C ;
Broder, S ;
Clark, AG ;
Nadeau, C ;
McKusick, VA ;
Zinder, N ;
Levine, AJ ;
Roberts, RJ ;
Simon, M ;
Slayman, C ;
Hunkapiller, M ;
Bolanos, R ;
Delcher, A ;
Dew, I ;
Fasulo, D ;
Flanigan, M ;
Florea, L ;
Halpern, A ;
Hannenhalli, S ;
Kravitz, S ;
Levy, S ;
Mobarry, C ;
Reinert, K ;
Remington, K ;
Abu-Threideh, J ;
Beasley, E .
SCIENCE, 2001, 291 (5507) :1304-+
[37]   GENETIC ALTERATIONS DURING COLORECTAL-TUMOR DEVELOPMENT [J].
VOGELSTEIN, B ;
FEARON, ER ;
HAMILTON, SR ;
KERN, SE ;
PREISINGER, AC ;
LEPPERT, M ;
NAKAMURA, Y ;
WHITE, R ;
SMITS, AMM ;
BOS, JL .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 319 (09) :525-532
[38]   Trapping human ribosomal protein genes [J].
Warner, JR ;
Nierras, CR .
GENOME RESEARCH, 1998, 8 (05) :419-421
[39]  
WHITEHEAD RH, 1987, IN VITRO CELL DEV B, V23, P436
[40]  
Wool IG, 1996, TRENDS BIOCHEM SCI, V21, P164, DOI 10.1016/S0968-0004(96)20011-8