于新平,马腾,周平坤,吴玉梅.宫颈癌细胞放射损伤后IER5蛋白表达及其相互作用蛋白的筛选和验证[J].中华放射医学与防护杂志,2017,37(4):246-250
宫颈癌细胞放射损伤后IER5蛋白表达及其相互作用蛋白的筛选和验证
Preliminary screening of novel IER5 interacting proteins after ionizing irradiation
投稿时间:2016-11-11  
DOI:10.3760/cma.j.issn.0254-5098.2017.04.002
中文关键词:  宫颈癌  IER5  免疫共沉淀  质谱分析
英文关键词:Cervical cancer  Immediate early response 5  Immuniprecipitation  Mass spectrometry
基金项目:国家自然科学基金(81272888);北京市医院管理局临床医学发展专项经费(ZYLX201705)
作者单位E-mail
于新平 100006 北京 首都医科大学附属北京妇产医院  
马腾 100850 北京 军事医学科学院放射与辐射医学研究所 放射生物学北京市重点实验室  
周平坤 100850 北京 军事医学科学院放射与辐射医学研究所 放射生物学北京市重点实验室  
吴玉梅 100006 北京 首都医科大学附属北京妇产医院 wym597118@163.com 
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中文摘要:
      目的 了解IER5蛋白经放射损伤后的表达变化,并筛选IER5蛋白在放射损伤后可能参与DNA损伤修复通路中的相互作用蛋白。方法 HeLa细胞经4 Gy γ射线照射后在不同时间点收集细胞,提取总蛋白质和细胞核蛋白行Western blot检验;构建3×Flag标签融合表达的IER5蛋白表达载体,转染人肾上皮细胞293T并照射,收集细胞行免疫沉淀富集IER5的结合蛋白,十二烷基磺酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分离免疫共沉淀复合物,考马斯亮蓝染色观察差异条带并切胶酶解后行质谱分析,对可能相互作用蛋白结果进行Western blot验证。结果 IER5蛋白照后4 h表达逐渐增加,12 h至高峰,持续至48 h;细胞核内IER5蛋白表达也有增加趋势;质谱分析数据表明,照射组检测出374个蛋白,对照组检测出256个蛋白,两组比较差异蛋白41个,照射组中包括与DNA结合、代谢、损伤修复相关的10个蛋白;其中,与DNA损伤修复密切相关的1型聚ADP核糖基化聚合酶(PARP1)得到Western blot验证。结论 IER5是放射损伤相关蛋白,其可能参与DNA损伤修复通路。
英文摘要:
      Objective To investigate the expression of radiation-induced IER5 protein and screen its potential interaction proteins that may participate in DNA repair process. Methods HeLa cells were irradiated with 4 Gy ionizing radiation. IER5 protein expression in whole cell lysate and in nuclear fraction were detected by Western blot at different timepoints after irradiation. 3×Flag-IER5 pCMV plasmid was constrcuted and the Flag tagged-IER5 expression was verified by Western blot. 293T cells were transfected with 3×Flag-IER5 pCMV plasmid. After irradiation the cells were collected and proteins were extracted. The IER5 interaction proteins were purified using immunoprecipitation and separated by 12% SDS-polyacrylamide gel electrophoresis. Then the binding proteins were cut from the gel and analyzed by Mass spectrometry. Results The expression of IER5 protein began to increase 4 hour post-irradiation and its peak level was observed at 12 hour post-irradiation, and it lasted until 48 hour after irradiation. The expression level of IER5 protein in whole cell lysate and nuclear fraction were both increased. With the mass spectrometry analysis, a total of 347 proteins and 256 proteins were identified in irradiated and non-irradiated groups, respectively. Fourty one differential proteins were obtained, where 10 proteins were associated with DNA metabolic process and DNA rapair in the irradiated group and the poly(ADP-ribose) polymerase 1 (PARP1) protein was further confirmed by Western blot. Conclusions IER5 protein is an DNA damage related protein, and it may participate in DNA repair process.
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