期刊文献+

氨基酰-tRNA合成酶编校相关的生理、病理效应和药物设计

Physiology,pathology and drug design related with editing of aminoacyl-tRNA synthetase
下载PDF
导出
摘要 氨基酰-tRNA合成酶(aaRS)催化tRNA的氨基酰化反应,为生物体内蛋白质合成提供原料。许多aaRS为保持蛋白质翻译的精确性,在进化的选择压力下产生了编校功能。近年来,人们越来越多关注aaRS编校功能同人类健康之间的关系。在过去的几年中,对于aaRS编校功能缺陷在细胞内的生理效应,与疾病发生的关系和以编校活性位点作为药靶设计、开发新型抗生素的研究中取得了重要的进展。 Aminoacyl-tRNA synthetases (aaRSs) catalyse aminoacylation of their cognate tRNAs for protein biosynthesis. Many aaRSs developed editing function under the stress of evolutionary selection for translation fidelity. Recently, the investigators pay more attention to the relation between the editing function and human health. Here, a few impressive progresses in understanding the cell physiology, pathology and drug design related with editing function of aminoacyl-tRNA synthetase were reviewed.
作者 姚鹏 王恩多
出处 《生命科学》 CSCD 2008年第4期667-672,共6页 Chinese Bulletin of Life Sciences
基金 科技部重大科学研究计划(2006CB 910301) 上海市科委资助项目(06JC14076)
关键词 氨基酰-TRNA合成酶 编校 生理 病理 药物设计 aminoacyl-tRNA synthetase editing physiology pathology drug design
  • 相关文献

参考文献28

  • 1Schimmel P, Ribas de Pouplana L. Formation of two classes of tRNA synthetases in relation to editing functions and genetic code. Cold Spring Harb Symp Quant Biol, 2001,66: 161-6.
  • 2Santos MA, Cheesman C, Costa V, et al. Selective advantages created by codon ambiguity allowed for the evolution of an alternative genetic code in Candida spp. Mol Microbiol, 1999, 31(3): 937-47.
  • 3Santos MA, Ueda T, Watanabe K, et al. The non-standard genetic code of Candida spp.: an evolving genetic code or a novel mechanism for adaptation? Mol Microbiol, 1997, 26 (3): 423-31.
  • 4Schimmel P. Aminoacyl-tRNA synthetases: general scheme of structure-function relationships in the polypeptides and recognition of transfer RNAs. Annu Rev Biochem, 1987, 56:125-58.
  • 5Ibba M, Soll D. Aminoacyl-tRNA synthesis. Annu Rev Biochem, 2000, 69:617-50.
  • 6Eriani G, Delarue M, Poch O, et al. Partition of tRNA synthetases into two classes based on mutually exclusive sets of sequence motifs. Nature, 1990, 347(6289): 203-6.
  • 7Eldred EW, Schimmel P. Rapid deacylation by isoleucyl transfer ribonucleic acid synthetase of isoleucine-specific transfer ribonucleic acid arninoacylated with valine. J Biol Chem, 1972, 247(9): 2961-4.
  • 8Fersht A, Kaetlmer M. Enzyme hyperspecificity. Rejection of threonine by the valyl-tRNA synthetase by misacylation and hydrolytic editing. Biochemistry, 1976, 15(15): 3342-6.
  • 9Chen JF, Guo NN, Li T, et al. Cl1 domain in Escherichia coli leucyl-tRNA synthetase is crucial for its editing function. Biochemistry, 2000, 39(22): 6726-31.
  • 10Beuning PJ, Musier-Forsyth K. Hydrolytic editing by a class II aminoacyl-tRNA synthetase. Proc Natl Acad Sci USA, 2000, 97(16): 8916-20.

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