Site-specific incorporation of a fluorescent terphenyl unnatural amino acid

Bioorg Med Chem Lett. 2015 Nov 15;25(22):5277-80. doi: 10.1016/j.bmcl.2015.09.050. Epub 2015 Sep 25.

Abstract

The site-specific incorporation of unnatural amino acids into proteins has a wide range of biological implications. Of particular interest is the incorporation of fluorescent probes as a mechanism to track protein function, transport, and folding. Thus, the development of a novel system for the incorporation of new fluorescent unnatural amino acids has significant utility. Specifically, we have elucidated an aminoacyl-tRNA synthetase capable of recognizing a terphenyl UAA derivative, and charging a cognate tRNA with this amino acid for protein incorporation. Moreover, we have successfully incorporated this fluorescent UAA into GFP at several key residues, demonstrating a novel means to modulate fluorescence within the protein.

Keywords: Aminoacyl-tRNA synthetase; Fluorescent sensors; Green fluorescent protein; Protein expression; Unnatural amino acids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Amino Acyl-tRNA Synthetases / genetics
  • Amino Acyl-tRNA Synthetases / metabolism*
  • Biphenyl Compounds / chemical synthesis*
  • Biphenyl Compounds / metabolism
  • Escherichia coli
  • Fluorescent Dyes / chemical synthesis*
  • Fluorescent Dyes / metabolism
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism*
  • Mutagenesis, Site-Directed
  • Mutation
  • Phenylalanine / analogs & derivatives*
  • Phenylalanine / chemical synthesis
  • Phenylalanine / metabolism
  • Protein Structure, Tertiary
  • Terphenyl Compounds / chemical synthesis*
  • Terphenyl Compounds / metabolism

Substances

  • 4-biphenyl-l-phenylalanine
  • Biphenyl Compounds
  • Fluorescent Dyes
  • Terphenyl Compounds
  • Green Fluorescent Proteins
  • Phenylalanine
  • Amino Acyl-tRNA Synthetases