Discovering differential protein expression caused by CagA-induced ERK pathway activation in AGS cells using the SELDI-ProteinChip platform

查看全文 作　　者：Zhen [1,3]Ge;Yong-Liang [2]Zhu;Xian [1]Zhong;Jie-Kai [1]Yu;Shu [1]Zheng

机构地区：[1]Cancer Institute,Second Affiliated Hospital, School of Medicine, ZhejiangUniversity, Hangzhou 310009, Zhejiang Province, China;[2]Gastroenterological Department, Second Affiliated Hospital, School of Medicine, Zhejiang University,Hangzhou 310009, Zhejiang Province, China;[3]Institute of Genome Sciences,College of Life Sciences, Zhejiang University, Hangzhou 310008,Zhejiang Province, China

出　　处：《World Journal of Gastroenterology》索引2008年第14卷第4期,共9页

基　　金：National High Technology 2006AA02Z341 & NSFC 30430730 摘　　要：AIM: To identify the protein expression differences related to the CagA-induced ERK pathway activation in AGS cells. METHODS: Human AGS cells transfected with cagA and blank vector were treated with specific mitogen-activated protein kinase kinase (MEK) inhibitor. Total cell proteins were combined by strong anion exchange (SAX2) and weak cation exchange (CM10) ProteinChip arrays and analyzed using surface-enhanced laser desorption/ ionization time-of-flight mass spectrometry (SELDI-TOF-MS) proteomics technology. Protein expression profi les were compared with those of inhibitor-untreated cagA transfectants. SwissProt/TrEMBL database searching for differentially expressed proteins was carried out using the TagIdent tool with the pI and mass information. RESULTS: When a total of 16 proteins that showed expression differences in inhibitor-untreated cagA transfectants were compared with vector transfectants,three proteins with m/z 4229,8162 and 9084 were found to have no expression differences after treatment with MEK inhibitor,while the other 13 maintained the same expression differences after inhibitor treatment. Seven pieces of meaningful matching information for the three proteins were obtained from database searching. CONCLUSION: Biomarkers with m/z 4229,8162 and 9084 are ERK1/2 phosphorylation dependent,and therefore are the downstream molecules of ERK1/2 in the ERK/MAPK signaling pathway. The three biomarkers may be important cancer-associated proteins according to SwissProt/TrEMBL database information. 关键词：激酶 AGS细胞 CAGA 蛋白质切片

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Discovering differential protein expression caused by CagA-induced ERK pathway activation in AGS cells using the SELDI-ProteinChip platform

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