期刊文献+

tRNA介导蛋白质工程 被引量:2

tRNA-mediated protein engineering(TRAMPE)
下载PDF
导出
摘要 在遗传信息从DNA到蛋白质流动的过程中 ,tRNA携带特异的氨基酸参与蛋白质合成 ,对于维持蛋白质翻译的忠实性起着非常重要的作用。生物体内共有 2 0种氨酰tRNA合成酶 ,每一种均对应于一种氨基酸和一个tRNA类型。但是这种翻译过程仅仅限于 2 0种天然氨基酸 ,因此在进行传统的蛋白质工程研究时常常受到限制。事实上 ,在蛋白质工程中借助于校正tRNA定点掺入非天然氨基酸可以提供蛋白质的结构信息 ,改进蛋白质检测与分离的方法 ,甚至赋予蛋白质某些新的特性。随着生物技术的发展和完善 ,tRNA介导蛋白质工程将不仅在蛋白质工程中发挥潜能 ,而且在研制新型生物材料和疾病诊断及药物治疗方面起到推动作用。 During the genetic information flow from DNA to proteins,tRNAs mediate protein synthesis with specific amino acid at its 3′ terminus,which is of pivotal role in maintaining the fidelity of protein translation.Each organism has 20 aminoacyl\|tRNA synthetases,each corresponding to an amino acid and its cognate tRNA.However,the translation process is circumvented in traditional protein engineering due to restriction of 20 natural amino acids.In fact,by virture of orthogonal suppressor tRNA,site\|directed non\|natural amino acid replacement(site\|directed NAAR)in predetermined sites in proteins can provide important structural information or greatly enhance the efficiency of protein assay and isolation.It can even creat proteins with some new chemical activities.TRAMPE will definitely be potential in the protein engineering,novel biomaterials,clinical diagnosis and therapy.\;
出处 《生物工程进展》 CSCD 2001年第1期11-14,共4页 Progress in Biotechnology
基金 国家自然科学基金项目(No.39730120)资助
关键词 tRNA介导蛋白质工程 校正tRNA 定点非天然氨基酸替代 蛋白质检测和分离 TRAMPE suppressor tRNA site-directed non-natural amino acid replacement protein assay and isolation
  • 相关文献

参考文献12

  • 1[1]Thrift R. N. et al. J. Cell Biol. 1991,112: 809-821.
  • 2[2]Cload S. T. et al. Chem. Biol. 1996,3:1033-1038.
  • 3[3]Anthony S.J. et al.TIBS. 1990,14:400-403.
  • 4[4]Kowal A. K. et al Nucleic Acids Res. 1997,25:4685-4689.
  • 5[5]Cornish V. W. et al. Proc. Natl. Acad. Sci USA. 1994,91: 2910-2914.
  • 6[6]Steward L.E. et al.J.Am Chem. Soc. 1997,119:6-11.
  • 7[7]Gallivan J. P. et al. Chem. Biol. 1997,4:739-749.
  • 8[8]England, P. M. et al. Proc. Natl. Acad. Sci. USA. 1997, 94:11025-11030.
  • 9[9]Mamaev S. V. et al. J. Am. Chem. Soc. 1996,118: 7243-7244.
  • 10[10]Hoeltke H.J. et al. Biotechniques. 1995,18:900-907.

同被引文献26

  • 1孙博,王捷.蛋白质分子体外定向进化研究进展[J].实用医学杂志,2006,22(11):1335-1336. 被引量:2
  • 2Brannigan JA,Wilkinson A J.Protein engineering 20 years on[J].Molecular Cell Biology,2002,3:964.
  • 3Szymkowski D E.Rational optimization of proteins as drugs:a new era of ‘medicinal biology'[J].Drug Discov Today,2004,9:381.
  • 4Wang K,Subbaiah PV.Importance of the free sulfhydryl groups of lecithin-cholesterol acyltransferase for its sensitivity to oxidative inactivation[J].Biochim Biophys Acta,2000,1488 (3),268.
  • 5Bogin O,Levin I,Hacham Y,er ae.Structural basis for the enhanced thermal stability of alcohol dehydrogenase mutants from the mesophilic bacterium Clostridium beijerinckii:contribution of salt bridging.[J] Protein Sci,2002,11(11):2561.
  • 6Holle LM.[Pegaspargase:analternative?[J].Ann Pharma -cother,1997,31(5):616.
  • 7Harris Jennifer L Craik Charles S.Engineering enzyme specificity[J].Current Opinion in Chemical Biology,1998:2,127.
  • 8Reidhaar-Olson J F Davis R M,De Souza-Hart J A,et al.Active variants of human parathyroid hormone (1-34) with multiple amino acid substitutions[J].Molecular and Cellular Endocrinology,2000,160.135.
  • 9John R Murphy,Protein engineering and design for drug delivery[J].Current Opinion in Structural Biology,1996,6:541.
  • 10Halin C,Rondini S,Nilsson F,et al.Enhancement of the antitumor activity of interleukin-12 by targeted delivery to neovasculature[J].Nature biotechnology,2002,20(3):264.

引证文献2

二级引证文献7

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