Convenient Access to Fluorescent Probes by Chemoselective Acylation of Hydrazinopeptides: Application to the Synthesis of the First Far-Red Ligand for Apelin Receptor Imaging

Chemistry. 2016 Jan 22;22(4):1399-405. doi: 10.1002/chem.201503630. Epub 2015 Dec 18.

Abstract

Herein, we develop a convenient method to facilitate the solution-phase fluorescent labelling of peptides based on the chemoselective acylation of α-hydrazinopeptides. This approach combines the advantages of using commercially available amine-reactive dyes and very mild conditions, which are fully compatible with the chemical sensitivity of the dyes. The usefulness of this approach was demonstrated by the labelling of apelin-13 peptide. Various fluorescent probes were readily synthesized, enabling the rapid optimization of their affinities for the apelin receptor. Thus, the first far-red fluorescent ligand with sub-nanomolar affinity for the apelin receptor was characterized and shown to track the receptor efficiently in living cells by fluorescence confocal microscopy.

Keywords: G-protein-coupled receptors; chemical ligation; fluorescent probes; hydrazinopeptides; receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acylation
  • Fluorescent Dyes / chemistry*
  • Hydrazines / chemical synthesis
  • Hydrazines / chemistry*
  • Intercellular Signaling Peptides and Proteins / chemistry*
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Ligands
  • Peptides / chemical synthesis*
  • Peptides / chemistry
  • Receptors, G-Protein-Coupled / chemistry*
  • Receptors, G-Protein-Coupled / metabolism

Substances

  • Fluorescent Dyes
  • Hydrazines
  • Intercellular Signaling Peptides and Proteins
  • Ligands
  • Peptides
  • Receptors, G-Protein-Coupled
  • apelin-13 peptide