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N-Acetyl lysyl-tRNA synthetases evolved by a CcdB-based selection possess N-acetyl lysine specificity in vitro and in vivo

  作者 Umehara, T; Kim, J; Lee, S; Guo, LT; Soll, D; Park, HS  
  选自 期刊  FEBS Letters;  卷期  2012年586-6;  页码  729-733  
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[摘要]Posttranslational modifications play a crucial role in modulating protein structure and function. Genetic incorporation of unnatural amino acids into a specific site of a protein facilitates the systematic study of protein modifications including acetylation. We here report the directed evolution of pyrrolysyl-tRNA synthetase (PylRS) from Methanosarcina mazei to create N-acetyl lysyl-tRNA synthetases (AcKRSs) using a new selection system based on the killing activity of the toxic ccdB gene product. The amino acid specificity of these and of published [1,2] AckRSs was tested in vitro and in vivo, and the enzyme-kinetic properties of the AckRSs were evaluated for the first time. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

 
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