期刊文献+

功能性包涵体的研究进展 被引量:6

Advances in the Study of non-classical Inclusion Bodies
原文传递
导出
摘要 利用原核系统表达外源重组蛋白的一个特点是表达蛋白多以包涵体形式存在。在过去人们一直认为包涵体是错误折叠、无生物活性的蛋白,需要经过变复性的过程重新获得有生物活性、可溶的蛋白,因而变复性条件的摸索迄今仍然是该领域的难点。但近几年的研究表明包涵体并非都是无生物活性的,功能性包涵体(或者称为非传统意义包涵体)概念的提出是该领域的一个重大研究进展。由于功能性包涵体本身具有生物活性,可在非变性条件下提取,目前已经在生命科学的基础研究、生物制药、生物材料、生物催化等领域展现出良好的应用前景。重点从功能性包涵体的定义、形成机理、提取条件等近期研究进展进行综述,以期为原核细胞表达和工业生产重组蛋白药物提供新的思路。 Expression of heterologous genes in prokaryotic cell is a fast,simple and cheap way to produce large amount of target proteins,especially recombinant protein drugs.However,overexpression of recombinant protein often leads to the formation of aggregates called inclusion bodies(IBs).In the past,IBs were recognized as deposits of misfolded and inactive proteins,and denaturation/renaturantion steps is necessary for isolation of biologically active protein.Until recently,IBs have been described as biological activity,which can be extracted from non-denaturing conditions,named non-classical Inclusion bodies(ncIBs).This review which focuses on the definition,mechanism and extraction of ncIBs is expected to provide valuable references for the research and exploit of recombination protein productions.
出处 《中国生物工程杂志》 CAS CSCD 北大核心 2013年第1期114-121,共8页 China Biotechnology
基金 "十二五"重大新药创制科技重大专项项目资助(2011ZX09506-007)
关键词 功能性包涵体 非变性 生物活性 non-classical Inclusion bodies(ncIBs) non-denature Bioactivity
  • 相关文献

参考文献45

  • 1Jev(s)evar S,Gaberc-Porekar V,Fonda I. Production of nonclassical inclusion bodies from which correctly folded protein can be extracted[J].Biotechnology Progress,2005,(02):632-639.doi:10.1021/bp0497839.
  • 2García-Fruitós E,González-Montalbán N,Morell M. Aggregation as bacterial inclusion bodies does not imply inactivation of enzymes and fluorescent proteins[J].MicrobvCell Fact,2005,(01):27-32.
  • 3Umetsu M,Tsumoto K,Nittaa S. Nondenaturing solubilization of beta2 microglobulin from inclusion bodies by L-arginine[J].Biochemical and Biophysical Research Communications,2005,(01):189-197.
  • 4Petemel (S),Bele M,Gaberec-Porekar V. Nonclassical inclusion bodies in Escherichia coli[J].Microbial Cell Factories,2006.23-24.
  • 5García-Fruitós E,Arís A,Villaverde A. Localization of functional polypeptides in bacterial inclusion bodies[J].Applied and Environmental Microbiology,2007,(01):289-294.
  • 6Petemel (S),Grdadolnik J,Gaberc-Porekar V. Engineering inclusion bodies for non denaturing extraction of functional proteins[J].Microbial Cell Factories,2008,(01):34-42.
  • 7DM W,NH G. The formation of biologically active beta-galactosidase inclusion bodies in Escherichia coli[J].Australian Journal of Biotechnology,1989,(01):28-32.
  • 8Tokatlidis K,Dhurjati P,Millet J. High activity of inclusion bodies formed in Ecoli overproducing Clostridium thermocellum endoglucanase D[J].FEBS Letters,1991,(01):205-208.
  • 9González-Montalbán N,García-Fruitós E,Villaverde A. Recombinant protein solubility--does more mean better[J].Nature Biotechnology,2007,(07):718-720.
  • 10Kopito R R. Aggresomes,inclusion bodies and protein aggregation[J].Trends in Cell Biology,2000,(12):524-530.doi:10.1016/S0962-8924(00)01852-3.

同被引文献54

  • 1李文卉,罗建勋,殷宏,关贵全,马米玲,刘志杰,刘爱红,党志胜,高金亮,任巧云.微小牛蜱Bm86基因的真核表达[J].中国兽医科技,2005,35(9):718-722. 被引量:4
  • 2朱红裕,李强.外源蛋白在大肠杆菌中的可溶性表达策略[J].过程工程学报,2006,6(1):150-155. 被引量:59
  • 3程太平,荣俊,刘晓娜,邹浩勇,齐晓亮,樊友净.IBDV VP2基因重组质粒pBV220表达条件的优化[J].动物医学进展,2007,28(4):9-13. 被引量:3
  • 4诸姮,胡宏友,卢昌义,李雄.植物体内的黄酮类化合物代谢及其调控研究进展[J].厦门大学学报(自然科学版),2007,46(A01):136-143. 被引量:83
  • 5樊瑞泉,罗建勋,杨孝朴,殷宏,高金亮,关贵全,刘志杰,党志胜,马米玲,任巧云,刘爱红.微小牛蜱Bm86基因的克隆与原核表达[J].甘肃农业大学学报,2007,42(1):15-19. 被引量:7
  • 6邓国藩 姜在阶.中国经济昆虫志[M].北京:科学出版社,1991.307.
  • 7DarnellJ[Jr, Kerr 1M, Stark GR.Jak-STAT pathways and transcriptional activation in response to IFNs and other extracellular signaling proteins[J]' Science, 1994, 264 (5146): 1415-142l.
  • 8Mark DF, Lu SD, Creasey AA, et al. Site specific mutagenesis of human fibroblast interferon gene[lJ. Proc Natl Acad Sci, 1984, 81 (18): 5662-5666.
  • 9Uehara A, Sugawara S, Takada H. Priming of human oral epithelial cells by interferon-gamma to secrete cytokines in response to lipopolysaccharides , lipoteichoic acids and peptidoglycans[J].J Med Microbiol , 2002, 51 (8): 626- 634.
  • 10Sunttha K, Chung BH,Jang KH, et al. Refolding and purification of zymomonas mobilis levansucrase produced as inclusion bodies in fed-batch culture of recombinant Escherichia coli[lJ. Protein Expr Purif , 2000, 18 (3): 338-393.

引证文献6

二级引证文献12

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