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通过RNA干扰下调真核释放因子1(eRF1)可提高人细胞中错酰化tRNA的抑制效率。

Downregulation of eRF1 by RNA interference increases mis-acylated tRNA suppression efficiency in human cells.

作者信息

Ilegems Erwin, Pick Horst M, Vogel Horst

机构信息

Institute of Biomolecular Sciences, Swiss Federal Institute of Technology, CH-1015 Lausanne, Switzerland.

出版信息

Protein Eng Des Sel. 2004 Dec;17(12):821-7. doi: 10.1093/protein/gzh096. Epub 2005 Feb 16.

Abstract

The site-specific incorporation of non-natural amino acids into proteins by nonsense suppression has been widely used to investigate protein structure and function. Usually this technique exhibits low incorporation efficiencies of non-natural amino acids into proteins. We describe for the first time an approach for achieving an increased level of nonsense codon suppression with synthetic suppressor tRNAs in cultured human cells. We find that the intracellular concentration of the eukaryotic release factor 1 (eRF1) is a critical parameter influencing the efficiency of amino acid incorporation by nonsense suppression. Using RNA interference we were able to lower eRF1 gene expression significantly. We achieved a five times higher level of amino acid incorporation as compared with non-treated control cells, as demonstrated by enhanced green fluorescent protein (EGFP) fluorescence recovery after importing a mutated reporter mRNA together with an artificial amber suppressor tRNA.

摘要

通过无义抑制将非天然氨基酸位点特异性地掺入蛋白质中已被广泛用于研究蛋白质的结构和功能。通常,该技术在非天然氨基酸掺入蛋白质方面表现出较低的掺入效率。我们首次描述了一种在培养的人细胞中使用合成抑制性tRNA提高无义密码子抑制水平的方法。我们发现真核释放因子1(eRF1)的细胞内浓度是影响通过无义抑制掺入氨基酸效率的关键参数。使用RNA干扰,我们能够显著降低eRF1基因的表达。与未处理的对照细胞相比,我们实现了高五倍的氨基酸掺入水平,这通过导入突变的报告mRNA和人工琥珀抑制性tRNA后增强绿色荧光蛋白(EGFP)荧光恢复得到证明。

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