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作 者:吴双[1] 开妍[1] 王晓泉[1] 胡顺林[1] 刘秀梵[1]
机构地区:[1]扬州大学农业部畜禽传染病学重点开放实验室,江苏扬州225009
出 处:《中国家禽》2010年第10期25-29,共5页China Poultry
基 金:国家自然科学基金重点项目(30630048);"十一五"国家支撑计划项目(2006BAD06A03)
摘 要:为了研究新城疫病毒(NDV)和宿主细胞之间的相互作用关系,本研究以NDV感染鸡胚成纤维细胞(CEF)为材料,对细胞培养方式、样品制备方法、上样量、等电聚焦以及凝胶染色等步骤进行一系列优化,建立了NDV感染CEF的双向凝胶电泳技术。运用PDQuest8.0.1软件对电泳图谱分析后显示:17cmIPG胶条(pH4~7)对应的凝胶上可检测到800个左右蛋白点、蛋白点匹配率达90%,表明NDV感染CEF蛋白质组双向凝胶电泳模型稳定、分辨率高、重复性好。电泳图谱上共发现36个差异表达明显的蛋白点,其中上调表达蛋白点有16个,下调表达蛋白点15个,新出现蛋白点3个,消失蛋白点为2个。NDV感染CEF双向凝胶电泳技术的建立为NDV的致病机理研究提供了有力的工具。To establish a stable technique of two-dimensional gel electrophoresis (2-DE)for chicken embryo fibroblasts (CEF) infected with Newcastle disease virus (NDV),eett culture,sample preparation,loading capacity,isoelectric focusing, staining and other steps were optimized using NDV-infected CEF as model system. About 800 protein spots on 17 cm IPG strip (pH 4 to 7) stained with blue sliver were analyzed by the software PDQuest8.0.1 ,and the match rate of protein spots was over 90%. The analysis of multiple 2-DE gets revealed that a total of 36 protein spots differentially expressed during NDV infection,including 16 up-regulated protein spots,15 down-regulated protein spots,3 new emerging protein spots and 2 disappear protein spots. Those differentially expressed protein spots were useful to further investigation of the interaction between NDV and its hosts.
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