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Proteomic Analysis of the Aging-related Proteins in Human Normal Colon Epithelial Tissue

  • Li, Ming (Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University) ;
  • Xiao, Zhi-Qiang (Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University) ;
  • Chen, Zhu-Chu (Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University) ;
  • Li, Jian-Ling (Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University) ;
  • Li, Cui (Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University) ;
  • Zhang, Peng-Fei (Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University) ;
  • Li, Mao-Yu (Key Laboratory of Cancer Proteomics of Chinese Ministry of Health, Xiangya Hospital, Central South University)
  • Published : 2007.01.31

Abstract

In order to screen the aging related proteins in human normal colon epithelia, the comparative proteomics analysis was applied to get the two-dimensional electrophoresis (2-DE) profiles with high resolution and reproducibility from normal colon epithelial tissues of young and aged people. Differential proteins between the colon epithelia of two age groups were found with PDQuest software. The thirty five differential protein-spots were identified by peptide mass fingerprint (PMF) based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) and database searching. Among them there are sixteen proteins which are significantly up-regulated in the colonic mucosal epithelia of young people group, which include ATP synthase beta chain, electron transfer flavoprotein alpha-subunit, catalase, glutathione peroxidase 1, annexin A2 and heat shock cognate 71 kDa protein, etc.; There are nineteen proteins which are significantly up-regulated in the colonic mucosal epithelia of aged people group, which include far upstream element-binding protein 1, nucleoside diphosphate kinase B, protein disulfide-isomerase precursor and VDAC-2, etc.. The identified differential proteins appear to be involved in metabolism, energy generation, chaperone, antioxidation, signal transduction, protein folding and apoptosis. The data will help to understand the molecular mechanisms of human colon epithelial aging.

Keywords

References

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