FCCC LOGO Faculty Publications
Li XM , Patel BB , Blagoi EL , Patterson MD , Seeholzer SH , Zhang T , Damle S , Gao Z , Boman B , Yeung AT
Analyzing alkaline proteins in human colon crypt proteome.[erratum appears in J Proteome Res. 2004 Nov-Dec;3(6):1300 Note: Seehozer, Steven H [corrected to Seeholzer, Steven H]]
Journal of Proteome Research. 2004 Jul-Aug;3(4) :821-33
PMID: 15359737   
Back to previous list
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.
United States Journal Article