期刊文献+

多肽TAT与核定位信号介导的蛋白质入核递送 被引量:5

TAT Peptide and Nuclear Localization Signal Mediated Protein Delivery into Cell Nuclei
在线阅读 下载PDF
导出
摘要 增强型绿色荧光蛋白与蛋白质转导结构域TAT、SV40大T抗原的核定位信号以融合蛋白的形式在大肠杆菌中表达 ,纯化后转导A431细胞 ,大部分细胞核内都可以观察到绿色荧光 ,说明TAT NLS可以有效介导蛋白质的入核递送。这种蛋白质递送系统可望用于转录治疗等研究领域。 Enhanced green fluorescence protein was expressed in E.coli as a fusion protein with TAT peptide and the nuclear localization signal of SV40 large T antigen.When purified protein TAT-NLS-eGFP-His-6 was incubated with A431 cells,it was able to accumulate within most cells' nuclei.This type of protein delivery system may be of potential application as a tool for transcription therapy research.;
出处 《中国生物工程杂志》 CAS CSCD 2004年第5期61-63,19,共4页 China Biotechnology
基金 国家"973"计划资助项目 ( 2 0 0 2CB5 13 2 0 4)
  • 相关文献

参考文献8

  • 1Beerens A M J,Al Hadithy A F Y,Rots M G,et al.Protein transduction domain and their utility in gene therapy.Ctrr Gene Ther,2003.3(5):486-494
  • 2Caron N J,Torrente Y ,Camirand G,et al.Intracellular deliveg of a Tat-eGFP fusion protein into muscle cells.Mol Ther,2001,3(3):310-318
  • 3Ignatovich I A,Dizhe E B,Pavlotskaya A V,et a/.Complexes of plasmid DNA with basic domain 47-57 of the HIV- 1 Tat protein are transferred to mammalian cells by endocytosis-mediated pathways.J Biol Chem,2003,278(43):42625~42636
  • 4Gration J,Yu J,Griffith J W,et al.Cell-permeable peptides improve cellular uptake and therapeutic gene delivery of replicationdeficient viruses in cells and in riro.Nat Med,2003,9(3):357-362
  • 5Peitz M,Pfannkuche K,Rajewsky K,et al.Ability of the hydrophobic FGF and basic TAT peptides to promote cellular uptake of recombinant Cre recombinase:a tool for efficient genetic engineering of mammalian genomes.Proc Natl Acad Sci USA,2002,99(7):4489~449
  • 6Pandolfi P P.Transcription therapy for cancer.Oncogene,2001,20(24):3116-3127
  • 7Rebar E J,Huang Y,Hickey R,et al.Induction of angiogenesis in a mouse model using engineered transcription factors.Nat Med,2002,8(12):1427-1432
  • 8赵兴卉,朱旭东,刘娟,饶相君,黄培堂.一种特异识别SV40启动子的人工转录因子的构建[J].生物工程学报,2003,19(5):608-612. 被引量:6

二级参考文献14

  • 1Rolf O, Rainer R,Victor L. CTCF is a uniquely versatile transcripton regulator linker to ipigenetics and disease. Trends Genet, 2001,17(9) :520 - 527.
  • 2Roger R B, Carlos F B. Engineering polydacyl zine-finger transcription factors. Nat Biotechno1,2002,20(2):135- 141.
  • 3Miller J, McLachlan A D, Klug A A. Repetitive finc-binding domains in the protein transcription factor ⅢA from Xenopus oocytes.EMBO J, 1985,4:1609- 1614.
  • 4Aaron K. Zinc finger peptides for the regulation of gene expression. J Mol Biol,1999,293:215 - 218.
  • 5Herren W,Yang W P,Carlos F. Building zinc fingers by selection:toward a therapeutic application. Proc Natl Acad Sci USA, 1995,92(1) :344 - 348.
  • 6Martha L. B, Huang X H, Yen C et al. Exploring the DNA-binding specitleities of zinc fingers with DNA microarrays. Proc Natl Acad Sci USA ,2001,98(13) :7158 - 7163.
  • 7David J S, Carlos F B. Design of novel sequence-specific DNA-binding proteins. Curr Opin Chem Biol, 2000,4( 1 ):34- 39.
  • 8Mark I, Aaron K, Yen C. A rapid, generally applicable method to engineer zinc fingers illustrated by targeting the HIV-1 promoter. Nat Biotechnol, 2001,19(7) :656 - 660.
  • 9Mark I, Yen C. Rapid, high-throughput engineering of sequencespecific zinc finger DNA-binding proteins. Methods Enzymol, 2001,340:593 - 609.
  • 10Mark I, Yen C. Engineered zinc finger proteins that respond to DNA modification by HaeⅢ and Hhal methyltransferase enzymes. J Mol Biol,2000,295:417 - 477.

共引文献8

同被引文献52

  • 1李慧昕,王君伟,李宝臣,韩先杰,何海娟,李昭春.牛病毒性腹泻病毒P20和P14基因的克隆及序列分析[J].中国预防兽医学报,2005,27(2):124-129. 被引量:6
  • 2刘坤,姜颖,贺福初.脂筏在病毒感染中的作用[J].中国生物化学与分子生物学报,2006,22(10):767-771. 被引量:6
  • 3Wu SP,Fu AL,Wang YX,Yu LP,Jia PY,Li Q,Jin GZ,Sun MJ.A novel therapeutic approach to 6-OHDA-induced Parkinson's disease in rats via supplementation of PTD-conjugated tyrosine hydroxylase[J].中国生物学文摘,2006,20(10):33-33. 被引量:9
  • 4Miller J,McLachlan AD, Klug A. A.Repetitive zinc-binding domains in the protein transcription factor ⅢA from Xenopus oocytes [J].EMBO J, 1985,4(6):1609
  • 5Ansari AZ, Mapp AK. Modular design of artificial transcription factors[J]. Curr Opin Chem Biol, 2002,6(6):765
  • 6Choo Y, Sanchez-Garcia I, Klug A. In vivo repression by a sitespecific DNA-binding protein designed against an oncogenic sequence[J]. Nature, 1994,372:642
  • 7Kim JS,Pabo CO. Transcriptional repression by zinc finger peptides [J]. J Biol Chem, 1997,272(47):29795
  • 8Hawiger J. Noninvasive intracellular delivery of functional peptides and proteins[J]. Curr Opin Chem Biol, 1999,3(1):89
  • 9Green M, Loewenstein PM. Autonomous functional domains of chemically synthesized human immunodeficiency virus tat transactivator protein[J]. Cell, 1988,55(6):1179
  • 10Frankel AD, Pabo CO. Cellular uptake of the tat protein from human immunodeficiency virus[J]. Cell, 1988,55(6):1189

引证文献5

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部