16
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Evolving Orthogonal Suppressor tRNAs To Incorporate Modified Amino Acids.

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          There have been considerable advancements in the incorporation of noncanonical amino acids (ncAA) into proteins over the last two decades. The most widely used method for site-specific incorporation of noncanonical amino acids, amber stop codon suppression, typically employs an orthogonal translation system (OTS) consisting of a heterologous aminoacyl-tRNA synthetase:tRNA pair that can potentially expand an organism's genetic code. However, the orthogonal machinery sometimes imposes fitness costs on an organism, in part due to mischarging and a lack of specificity. Using compartmentalized partnered replication (CPR) and a newly developed pheS negative selection, we evolved several new orthogonal Methanocaldococcus jannaschii (Mj) tRNA variants tRNAs with increased amber suppression activity, but that also showed up to 3-fold reduction in promiscuous aminoacylation by endogenous aminoacyl-tRNA synthetases (aaRSs). The increased orthogonality of these variants greatly reduced organismal fitness costs associated in part due to tRNA mischarging. Using these methods, we were also able to evolve tRNAs that supported the specific incorporation of 3-halo-tyrosines (3-Cl-Y, 3-Br-Y, and 3-I-Y) in E. coli.

          Related collections

          Author and article information

          Journal
          ACS Synth Biol
          ACS synthetic biology
          American Chemical Society (ACS)
          2161-5063
          2161-5063
          January 20 2017
          : 6
          : 1
          Affiliations
          [1 ] Center for Systems and Synthetic Biology, University of Texas at Austin , Austin, Texas 78712, United States.
          Article
          10.1021/acssynbio.6b00145
          27600875
          2fa71cbe-88c5-46e8-bf45-42c3a7769f9d
          History

          aminoacyl-tRNA synthetase,noncanonical amino acids,orthogonal translation systems,tRNA

          Comments

          Comment on this article