Genetically encoding thyronine for fluorescent detection of peroxynitrite

Bioorg Med Chem. 2020 Sep 15;28(18):115665. doi: 10.1016/j.bmc.2020.115665. Epub 2020 Jul 29.

Abstract

Peroxynitrite is a highly reactive oxidant effecting cell signaling and cell death. Here we report a fluorescent protein probe to selectively detect peroxynitrite. A novel unnatural amino acid, thyronine (Thy), was genetically encoded in E. coli and mammalian cells by evolving an orthogonal tRNAPyl/ThyRS pair. Incorporation of Thy into the chromophore of sfGFP or cpsGFP afforded a virtually non-fluorescent reporter. Upon treatment with peroxynitrite, Thy was converted into tyrosine via O-dearylation, regenerating GFP fluorescence in a time- and concentration-dependent manner. Genetically encoded thyronine may also be valuable for other redox applications.

Keywords: Fluorescence; Genetic code expansion; Peroxynitrite; Thyronine; Unnatural amino acid.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Escherichia coli
  • Fluorescent Dyes / chemistry*
  • Green Fluorescent Proteins / chemistry*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Hydrogen Peroxide / chemistry
  • Kinetics
  • Limit of Detection
  • Oxidation-Reduction
  • Peroxynitrous Acid / analysis*
  • RNA, Transfer
  • Thyronines / chemistry*
  • Tyrosine / chemistry

Substances

  • Fluorescent Dyes
  • Thyronines
  • Peroxynitrous Acid
  • Green Fluorescent Proteins
  • Tyrosine
  • RNA, Transfer
  • Hydrogen Peroxide