首页 | 本学科首页   官方微博 | 高级检索  
检索        

人表皮生长因子受体2模拟表位的筛选
引用本文:李晓霞,师建国,陈 果,贺雪姣.人表皮生长因子受体2模拟表位的筛选[J].现代肿瘤医学,2015,0(12):1644-1646.
作者姓名:李晓霞  师建国  陈 果  贺雪姣
作者单位:第四军医大学基础医学部病理生理学教研室,陕西 西安 710032
摘    要:目的:从噬菌体12肽库中筛选出人表皮生长因子受体2(Her2)的抗原模拟表位。方法:以曲妥珠单抗为靶分子,在噬菌体12肽库中进行3轮淘选,以ELISA方法及竞争抑制实验鉴定阳性克隆,并对阳性克隆株进行测序。结果:经过3轮淘选,与曲妥珠单抗结合的噬菌体得到了有效富集,回收率从(2.00×10-8)%增加到(2.87×10-5)%,ELISA显示20个克隆中筛选获得了18个与曲妥珠单抗具有较高亲和性的阳性噬菌体,对阳性克隆测序获得两种氨基酸序列:HTSSLWHLFRST、VHWDFRQWWQPS。结论:噬菌体展示技术可成功筛选到表皮生长因子2模拟表位,为探索乳腺癌的防治研究创造了条件。

关 键 词:表皮生长因子受体2  噬菌体肽库  模拟表位

Screening and identification of the minotops of human epidermal growth factor receptor 2
Li Xiaoxia,Shi Jianguo,Chen Guo,He Xuejiao.Screening and identification of the minotops of human epidermal growth factor receptor 2[J].Journal of Modern Oncology,2015,0(12):1644-1646.
Authors:Li Xiaoxia  Shi Jianguo  Chen Guo  He Xuejiao
Institution:Department of Pathophysiology,Faculty of Preclinical Medicine,Fourth Military Medical University,Shaanxi Xi'an 710032,China.
Abstract:Objective:To screen the minotops of Her2 from the phage display 12 peptide library.Methods:Used the Herceptin as the ligand to select the positive clones after 3 rounds of screening by the phage display 12 peptide library.The positive clones were identified by enzyme linked immunosorbent assay(ELISA) and competitive inhibition assay.The identified positive clones were analyzed by DNA sequencing.Results:The phages were effectively enriched after 3 rounds of planning with the improvement of the recovery rate was from(2.00×10-8)% to (2.87×10-5)%.In 20 individual phages,the 18 phages could combine the epidermal growth factor 2 monoclonal antibody.Two kinds of different sequences(HTSSLWHLFRST,VHWDFRQWWQPS) were obtained.Conclusion:The Her2 related antigen epitope is obtained by phage display technology.The result provides a new approach for breast cancer therapy and vaccine development.
Keywords:epidermal growth factor receptor 2  phagepeptide library  mimotopes
本文献已被 万方数据 等数据库收录!
点击此处可从《现代肿瘤医学》浏览原始摘要信息
点击此处可从《现代肿瘤医学》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号