Light-Controlled Traceless Protein Labeling via Decaging Thio- o-naphthoquinone Methide Chemistry

Org Lett. 2022 Sep 23;24(37):6816-6821. doi: 10.1021/acs.orglett.2c02742. Epub 2022 Sep 13.

Abstract

We report the molecular design of a novel multifunctional reagent and its application for light-controlled selective protein labeling. This molecule integrates functions of protein-ligand recognition, bioconjugation, ligand cleavage, and photoactivation by merging the photochemistries of 2-nitrophenylpropyloxycarbonyl and 3-hydroxymethyl-2-naphthol with an affinity ligand and fluorescein. Highly electrophilic o-naphthoquinone methide was photochemically released and underwent proximity-driven selective labeling with the protein of interest (e.g., carbonic anhydrases), which retains its native function after labeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbonic Anhydrases*
  • Fluoresceins
  • Ligands
  • Naphthoquinones
  • Proteins / chemistry
  • Tumor Necrosis Factor Ligand Superfamily Member 14*

Substances

  • 1,2-naphthoquinone
  • Carbonic Anhydrases
  • Fluoresceins
  • Ligands
  • Naphthoquinones
  • Proteins
  • Tumor Necrosis Factor Ligand Superfamily Member 14
  • 3-(hydroxymethyl)-2-naphthol