首页 | 本学科首页   官方微博 | 高级检索  
检索        

一种新型的具有免疫调节和介导DNA基因治疗的蛋白质载体的研制
引用本文:商学军,葛京平,黄卫东,姚根宏,李宏军,黄宇烽.一种新型的具有免疫调节和介导DNA基因治疗的蛋白质载体的研制[J].中华男科学杂志,2008,14(10):888-892.
作者姓名:商学军  葛京平  黄卫东  姚根宏  李宏军  黄宇烽
作者单位:1. 南京大学医学院临床学院/南京军区南京总医院,男科,江苏南京,210002
2. 南京大学医学院临床学院/南京军区南京总医院,泌尿外科,江苏南京,210002
3. 重庆佳音前列腺疾病科研所,重庆,400023
4. 南京大学医学院临床学院/南京军区南京总医院,输血科,江苏南京,210002
摘    要:目的:研制一种具有调节宿主免疫系统,同时又能包装核酸进入肿瘤细胞的新型蛋白质载体。方法:利用基因工程技术,将人乙肝病毒核心抗原(HBcAg)的-COOH端和靶向肿瘤的整和素配体RGD肽与谷胱甘肽还原酶(GST)在大肠埃希菌中融合表达,经分子筛和GST亲和纯化后,获得DNA包装蛋白GST-RGD-ΔHBcAg。此包装蛋白用FITC标记后与前列腺癌PC-3细胞孵育,观察进入细胞情况;并用此包装蛋白包装含绿色荧光蛋白GFP基因的DNA载体pEGFP-N1,转染PC-3细胞,观察绿色荧光蛋白表达。此外,用包装蛋白GST-RGD-ΔHBcAg免疫6周龄雌性BALB/c小鼠,检测血清IgG1和IgG2a抗体水平。结果:本研究应用原核表达系统成功地表达并纯化出DNA包装蛋白GST-RGD-ΔHBcAg;荧光显微镜下观察到包装蛋白GST-RGD-ΔHBcAg能进入到PC-3细胞,并能携带绿色荧光蛋白基因进入PC-3细胞并表达;该包装蛋白免疫BALB/c小鼠后,小鼠血清IgG1和IgG2a抗体水平同时升高。结论:本研究研制的DNA包装蛋白GST-RGD-ΔHBcAg可作为基因治疗载体,并能对宿主的免疫系统起调节作用,为肿瘤的免疫——基因治疗载体提供一个新的选择。

关 键 词:非病毒载体  RGD肽  乙肝病毒核心抗原  谷胱甘肽还原酶

Development of a Novel Protein Carrier Inducing Immune Response and Binding DNA in Gene Therapy
SHANG Xue-jun,GE Jing-ping,HUANG Wei-dong,YAO Gen-hong,LI Hong-jun,HUANG Yu-feng.Development of a Novel Protein Carrier Inducing Immune Response and Binding DNA in Gene Therapy[J].National Journal of Andrology,2008,14(10):888-892.
Authors:SHANG Xue-jun  GE Jing-ping  HUANG Wei-dong  YAO Gen-hong  LI Hong-jun  HUANG Yu-feng
Institution:SHANG Xue-jun, GE Jing-ping, HUANG Wei-dong, YAO Gen-hong, LI Hong-jun, HUANG Yu-feng(1. Department of Andrology, 2. Department of Urology, 4. Department of Immunohematology, School of Clinical Medicine, Nanjing University Medical College, Nanjing General Hospital of Nanjing Military Region, Nanjing, Jiangsu 210002, China; 3. Research Institute of Prostate Diseases, Jiayin Hospital, Chongqing 400023, China; 5. Department of Urology, Peking Union Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China)
Abstract:Objective : To develop a novel protein carrier which can not only regulate the immune system but also deliver DNA into the tumor ceil as an effective non-viral gene delivery system. Methods: By using gene engineering techniques, we constructed a fusion protein containing the -COOH end of human hepatitis B virus core antigen (HBcAg) , small home-to-cancer peptide ligand RGD and Glutathione S-transferase (GST) , which was expressed in E. coil and purified by size exclusion chromatography and affinity chromatog- raphy. We labeled it with FITC to observe whether it could bind prostate cancer PC-3 ceil lines, and meanwhile used it as a non-viral gene delivery carrier with the plasmid pEGFP-NI that could express GFP in PC-3 cells. Furthermore, we observed the regulatory func- tion of this fusion protein to the mouse immune system. Results : The results of SDS-PAGE showed that the new protein carrier was obtained, which It could enter PC-3 cells with DNA in vitro and induce the mouse immune system to produce IgG1 and IgG2ct simulta- neously. Conclusion: The new protein carrier can be used as a target protein, especially in positive cells and the immune system. It promises to be a good novel carrier for the gene therapy of cancer. Natl J Androl, 2008, 14(10) : 888-892
Keywords:non-virus delivery carrier  peptide ligand RGD  hepatitis B virus core antigen  Gluthatione S-transferase
本文献已被 维普 万方数据 等数据库收录!
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