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作 者:吕磊[1] 刘志强[1] 李丽[1] 刘宁[1] 刘淑莹[1]
机构地区:[1]中国科学院长春应用化学研究所新药研究实验室长春质谱中心
出 处:《高等学校化学学报》2006年第4期635-637,共3页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:20273067;20173057);中国科学院知识创新工程(批准号:KGCX2-SW-213-06)资助
摘 要:The proteomic maps of human ovarian adenocarcinoma cell line in Human COC1 and its cell subline COC1/DDP were produced by 2-DE SDS-PAGE.The image analysis revealed obviously differential protein expression of the cells in response to cisplatin treatment.Approximate 1 300 protein spots were resolved in the two ranges of pI(3—10).The spots which have 10-fold difference in light density were digested by in-gel(enzyme),identified by matrix assisted laser desorption/ionization time-of-flight mass spectrometry(MALDI-TOF-MS) and finally detected by Profound and Mascot search engine in IDI databases.Seven proteins with obviously altered abundances were detected specifically,including four up-regulated protein spots and three down-regulated protein spots.The proteins differentially expressed in the parent cell line COC1 and its subline COC1/DDP were considered to be important for the therapy and pathogenesis.The proteomic maps of human ovarian adenocarcinoma cell line in Human COC1 and its cell subline COC1/DDP were produced by 2-DE SDS-PAGE. The image analysis revealed obviously differential protein expression of the cells in response to cisplatin treatment. Approximate 1 300 protein spots were resolved in the two ranges of pl(3-10). The spots which have 10-fold difference in light density were digested by in-gel enzyme, identified by matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDITOF-MS) and finally detected by Profound and Mascot search engine in IDI databases. Seven proteins with obviously altered abundances were detected specifically, including four up-regulated protein spots and three down-regulated protein spots. The proteins differentially expressed in the parent cell line COC1 and its subline COC1/DDP were considered to be important for the therapy and pathogenesis.
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