Literature DB >> 24631543

Pyrrolysyl-tRNA synthetase: an ordinary enzyme but an outstanding genetic code expansion tool.

Wei Wan1, Jeffery M Tharp1, Wenshe R Liu2.   

Abstract

The genetic incorporation of the 22nd proteinogenic amino acid, pyrrolysine (Pyl) at amber codon is achieved by the action of pyrrolysyl-tRNA synthetase (PylRS) together with its cognate tRNA(Pyl). Unlike most aminoacyl-tRNA synthetases, PylRS displays high substrate side chain promiscuity, low selectivity toward its substrate α-amine, and low selectivity toward the anticodon of tRNA(Pyl). These unique but ordinary features of PylRS as an aminoacyl-tRNA synthetase allow the Pyl incorporation machinery to be easily engineered for the genetic incorporation of more than 100 non-canonical amino acids (NCAAs) or α-hydroxy acids into proteins at amber codon and the reassignment of other codons such as ochre UAA, opal UGA, and four-base AGGA codons to code NCAAs.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Amber codon; Genetic code expansion; Hydroxy acids; Non-canonical amino acids; Pyrrolysine

Mesh:

Substances:

Year:  2014        PMID: 24631543      PMCID: PMC4016821          DOI: 10.1016/j.bbapap.2014.03.002

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


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