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

Jean-François MargatheXavier IturriozPierre RegenassIuliia A KarpenkoNicolas HumbertHugues de RocquignyMarcel HibertCatherine Llorens-CortesDominique Bonnet
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2015)
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.
Keyphrases
  • living cells
  • fluorescent probe
  • single molecule
  • quantum dots
  • high resolution
  • small molecule
  • binding protein
  • label free
  • mass spectrometry
  • fluorescence imaging
  • photodynamic therapy