Irreversible Protein Labeling by Paal-Knorr Conjugation

Chembiochem. 2017 Sep 19;18(18):1792-1796. doi: 10.1002/cbic.201700210. Epub 2017 Aug 10.

Abstract

The application of new chemical reactions in a biological context has advanced bioconjugation methods for both fundamental research and commercial arenas. Recent adaptations of reactions such as Huisgen 1,3-dipolar or Diels-Alder cycloadditions have enabled the labeling of specific residues in biomolecules by the attachment of molecules carrying azides, alkynes, or strained alkenes. Although these are fundamental tools, there is a need for the discovery of reactions that can label native proteins. We report herein the adaptation of the Paal-Knorr reaction to label lysine residues in proteins via pyrrole linkages.

Keywords: Paal-Knorr reaction; biocompatible reactions; bioconjugation; click chemistry; protein labeling.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry
  • Amines / chemistry
  • Animals
  • Azides / chemistry
  • Catalysis
  • Cattle
  • Click Chemistry
  • Cycloaddition Reaction
  • Fluorescent Dyes / chemistry
  • HCT116 Cells
  • Humans
  • Microscopy, Confocal
  • Pyrroles / chemistry*
  • Serum Albumin, Bovine / chemistry

Substances

  • Alkynes
  • Amines
  • Azides
  • Fluorescent Dyes
  • Pyrroles
  • Serum Albumin, Bovine