期刊文献+

融合蛋白CTP-SOD在毕赤酵母中的表达、纯化及抗氧化能力 被引量:2

Expression and purification of fusion protein CTP-SOD in Pichia pastoris and antioxidant capacity analysis
原文传递
导出
摘要 超氧化物歧化酶(SOD)是一种在生物界广泛存在的抗氧化酶,在抗衰老、抗肿瘤、抗免疫疾病和电磁辐射上都起着重要的作用。本实验利用含有细胞质转导肽(CTP,一种能够携带外源大分子穿过细胞膜,定位于细胞质的短肽)基因序列的特异引物,以人总RNA反转录产物为模板,扩增出了CTP和人铜锌超氧化物歧化酶(Cu/Zn SOD)的融合基因。运用毕赤酵母表达系统成功表达了具有活性的CTP-SOD融合蛋白。CTP-SOD预处理HeLa细胞后,明显提高了邻苯三酚(Progallol)诱导氧化胁迫下HeLa细胞的存活率,和对照组野生型SOD相比具有显著性差异。结果表明,CTP-SOD融合蛋白比野生型SOD更容易进入细胞,具有更高效的抗氧化功能。 Cytoplasmic transduction peptide (CTP) is a newly designed transduction peptide, by which special molecules can be carried out and localized into cytoplasmic compartment. Superoxide dismutase (SOD) is a protein that is difficult to go into cytoplasm. In this study, CTP-SOD fusion gene was amplified from human cDNA by PCR, and the active recombinant protein was successfully expressed in Pichia pastoris. HeLa cells pretreated with CTP-SOD showed a significantly improved survival against the pyrogallol-induced oxidative stress, suggesting CTP-SOD could cross the cell membrane more efficiently and protect cells from oxidative stress.
出处 《生物工程学报》 CAS CSCD 北大核心 2010年第3期324-329,共6页 Chinese Journal of Biotechnology
基金 重庆市自然科学基金项目(No.CSTC2009BB1131)资助~~
关键词 细胞质转导肽 毕赤酵母 分泌表达 氧化胁迫 cytoplasmic transduction peptide Pichia pastoris secretory expression oxidative stress
  • 相关文献

参考文献12

  • 1Kim D, Jeon C, Kim JH, et al. Cytoplasmic transduction peptide (CTP): new approach for the delivery of biomolecules into cytoplasm in vitro and in vivo. Exp Cell Res, 2006, 312: 1277-1288.
  • 2Hallewell RA, Masiarz FR, Najarian RC, et al. Human Cu/Zn superoxide dismutase cDNA: isolation of clones synthesizing high levels of active or inactive enzyme from an expression library. Nucleic Acids Res, 1985, 13: 2017-2034.
  • 3王多宁,赵雁武,田芙蓉.考马斯亮蓝微盘比色法测定蛋白质含量[J].第四军医大学学报,2001,22(6):528-529. 被引量:82
  • 4Kim SW, Han YW, Lee ST, et al. A superoxide anion generator, pyrogallol, inhibits the growth of HeLa cells via cell cycle arrest and apoptosis. Mol Carcinogen, 2008, 47: 114-125.
  • 5Vives E, Brodin P, Lebleu B. A truncated HIV-1 Tat protein basic domain rapidly translocates through the plasma membrane and accumulates in the cell nucleus. J Biol Chem, 1997, 272: 16010-16017.
  • 6Truant R, Cullen BR. The arginine-rich domains present in human immunodeficiency virus type 1 Tat and Rev function as direct importin beta-dependent nuclear localization signals. Mol Cell Biol, 1999, 19: 1210-1217.
  • 7Sandgren S, Cheng F, Belting M. Nuclear targeting of macromolecular polyanions by an HIV-Tat derived peptide. Role for cell-surface proteoglycans. J Biol Chem, 2002, 277: 38877-38883.
  • 8Potocky TB, Menon AK, Gellman SH. Cytoplasmic and nuclear delivery of a TAT-derived peptide and a beta-peptide after endocytic uptake into HeLa cells. JBiol Chem, 2003, 278: 50188-50194.
  • 9Ferrari A, Pellegrini V, Arcangeli C, et al. Caveolaemediated internalization of extracellular HIV-1 tat fusion proteins visualized in real time. Mol Ther, 2003, 8: 284-294.
  • 10Chauhan A, Tikoo A, Kapur AK, et al. The taming of the cell penetrating domain of the HIV Tat: myths and realities. J Control Rel, 2007, 117: 148-162.

二级参考文献3

  • 1Guo M L,生物化学与生物物理进展,1996年,23卷,6期,558页
  • 2Li H B,生物化学与生物物理进展,1993年,20卷,5期,402页
  • 3Ye Q L,临床检验杂志,1986年,4卷,3期,120页

共引文献81

同被引文献56

引证文献2

二级引证文献8

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