期刊文献+

PVP两亲性嵌段共聚物对超螺旋DNA的裂解活性

Cleavage Activity of PVP Amphiphilic Block Copolymer for Supercoiled DNA
原文传递
导出
摘要 以PVP-Cl为大分子引发剂,经ATRP聚合制备得到窄分子量分布、结构可控的含不同亲水/疏水比例的两亲性聚N-乙烯基吡咯烷酮-b-聚N-甲基丙烯酰基-N'-Boc-色氨酸酰胺基硫脲嵌段共聚物(PVP-b-PTrpAMT-I,II,III).1H NMR核磁共振、GPC-MALLS以及凝胶电泳对嵌段共聚物的结构进行了表征、对超螺旋质粒DNA的裂解行为进行了研究.结果表明PVP-b-PTrpAMT可以显著诱导超螺旋质粒DNA裂解,使超螺旋型DNA转变为缺口型,而缺口型DNA在基因转染过程中可有效避免其在细胞内被降解,提高转染效率.该嵌段共聚物对DNA的裂解活性与疏水链段含量、共聚物与DNA的质量比以及与DNA的共孵育时间有关. Amphiphilic block copolymers poly(N-vinylpyrrolidone)-block-poly(N-t-Boc-tryptophanamido-N'-methacryl thiourea)(PVP-b-PTrpAMT-I,II,III) were designed and synthesized with well defined structures by atom transfer radical polymerization(ATRP) using PVP-Cl as macroinitiator.The chemical structures of the block copolymers were characterized by 1H NMR and GPC-MALLS.Agarose gel electrophoresis study demonstrated that PVP-b-PTrpAMT can induce and cleavage supercoiled DNA into nicked DNA.The nicked DNA can avoid the degradation of DNA in the cell efficiently and have a potential ability to enhance the gene transfection.The cleavage activity of these block copolymers was obviously dependent on the different composition of the copolymer,quality ratio of the copolymer with plasmid DNA and the incubating time together with plasmid DNA.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2011年第16期1941-1945,共5页 Acta Chimica Sinica
基金 国家自然科学基金(No.20644002) 教育部博士点基金(No.20060486027) 兰州大学中央高校基本科研业务费专项(No.lzujbky-2009-27)和兰州大学交叉学科青年创新研究基金(No.LZUJC200911)资助项目
关键词 聚(N-乙烯基吡咯烷酮) 嵌段共聚物 DNA 裂解活性 poly(N-vinylpyrrolidone) block copolymer DNA cleavage activity
  • 相关文献

参考文献18

  • 1Felgner, P. L.; Barenholz, Y.; Behr, J. P.; Cheng, S. H.; Cullis, P.; Huang, L.; Jessee, J. A.; Seymour, L.; Szoka, F.; Thierry, A. R.; Wagner, E.; Wu, G. Hum. Gene Ther. 1997, 8,511. 被引量:1
  • 2Pitard, B.; Pollard, H.; Agbulut, O.; Kanbert, O.; Vilqulin, J T.; Cherel, Y.; Abadie, J.; Samuel, J. L.; Rigaud, J. L. Menoret, S.; Anegon, I.; Escande, D. Hum. Gene Ther 2002, 13, 1767. 被引量:1
  • 3Vincent, K. A.; Shyu, K. G.; Luo, Y.; Magner, M.; Tio, R. A.; Jiang, C.; Goldberg, M. A.; Akita, G. Y.; Gregory, R. J.; Isner, J. M. Circulation 2000, 102, 2255. 被引量:1
  • 4Williams, J. H.; Sirsi, S. R.; Latta, D. R.; Lutz, G. J. Mol. Ther. 2006, 14, 88. 被引量:1
  • 5崔亮,李洋,侯小东,宫文娟,徐宇虹,曹阿民.聚乙二醇嵌段树枝状聚赖氨酸共聚物的合成及其基因载体研究[J].化学学报,2007,65(19):2181-2186. 被引量:6
  • 6Kabanov, A. V.; Lemieux, P.; Vinogradov, S.; Alakhob, V. Adv. Drug Delivery Rev. 2002, 54, 223. 被引量:1
  • 7D'souza, A. J. M.; Schowen, R. L.; Topp, E. M. J. Controlled Release 2004, 94, 91. 被引量:1
  • 8Cifti, K.; Levy, R. J. Int. J. Pharm. 2001, 218, 81. 被引量:1
  • 9Lemieux, P.; Guerin, N.; Paradis, G.; Proul, R.; Chistyakova, L.; Kabanov, A.; Alakhov, V. Gene Ther. 2000, 7, 986. 被引量:1
  • 10Rijcken, C. J. F.; Soga, O.; Hennink, W. E. J. Controlled Release 2007, 120, 131. 被引量:1

二级参考文献14

  • 1Temin, H. M. Hum. Gene Ther. 1990, 1(2), 111. 被引量:1
  • 2E1-Aneed, A. J. Controlled Release 2004, 94(1), 1. 被引量:1
  • 3Smith, L. C.; Duguid, J.; Wadhwa, M. S.; Logan, M. J.; Tung, C. H.; Edwards, V.; Sparrow, J. T. Adv. Drug Delivery Rev. 1998, 30(1-3), 115. 被引量:1
  • 4Pouton, C. W.; Seymour, L. W. Adv. Drug Delivery Rev. 2001, 46(1-3), 187. 被引量:1
  • 5Kabanov, A. V. Pharm. Sci. Technol. Today 1999, 2(9), 365. 被引量:1
  • 6Sadler, K.; Tam, J. P. J. Biotechnol. 2002, 90(3-4), 195. 被引量:1
  • 7Li, Y.; Cui, L.; Li, Q. B.; Jia, L.; Xu, Y. H.; Fang, Q.; Cao, A. Biomacromolecules 2007, 8, 1409. 被引量:1
  • 8Rungsardthong, U.; Deshpande, M.; Biley, L.; Vamvakaki, M.; Armes, S. P.; Garnett, M. C.; Stolnik, S. J. Controlled Release 2001, 73(2~3), 359. 被引量:1
  • 9Lee, M.; Kim, S. W. Pharm. Res. 2005, 22, 1. 被引量:1
  • 10Bayer, E.; Mutter, M. The Liquid-Phase Method for Peptide Synthesis in the Peptides, Vol. 2, Eds.: Gross, E.; Meienhofer, J., Academic Press, New York, 1979, pp. 285-332. 被引量:1

共引文献22

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