Literature DB >> 16260173

Adding amino acids to the genetic repertoire.

Jianming Xie1, Peter G Schultz.   

Abstract

Considerable progress has been made in expanding the number and nature of genetically encoded amino acids in Escherichia coli, yeast and mammalian cells in the past four years. To date, over 30 unnatural amino acids have been cotranslationally incorporated into proteins with high fidelity and efficiency by means of a unique codon and corresponding orthogonal tRNA-aminoacyl-tRNA synthetase pair. The incorporated amino acids contain spectroscopic probes, post-translational modifications, metal chelators, photoaffinity labels and unique functional groups. The ability to genetically encode additional amino acids, beyond the common 20, provides a powerful approach for probing protein structure and function both in vitro and in vivo, as well as generating proteins with new or enhanced properties.

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Year:  2005        PMID: 16260173     DOI: 10.1016/j.cbpa.2005.10.011

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  39 in total

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Review 6.  Site-specific labeling of proteins with NMR-active unnatural amino acids.

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Journal:  J Biomol NMR       Date:  2009-06-16       Impact factor: 2.835

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9.  The Standard Genetic Code can Evolve from a Two-Letter GC Code Without Information Loss or Costly Reassignments.

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Review 10.  The alpha,alpha-difluorinated phosphonate L-pSer-analogue: an accessible chemical tool for studying kinase-dependent signal transduction.

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Journal:  Chem Biol       Date:  2009-09-25
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