Fiche publication
Date publication
novembre 2018
Journal
Organic & biomolecular chemistry
Auteurs
Membres identifiés du Cancéropôle Est :
Pr DENAT Franck
,
Dr GONCALVES Victor
,
Dr BELLAYE Pierre-Simon
Tous les auteurs :
Canovas C, Bellaye PS, Moreau M, Romieu A, Denat F, Goncalves V
Lien Pubmed
Résumé
Near-infrared (NIR) fluorescence imaging is a promising new medical imaging modality. Associated with a targeting molecule, NIR fluorophores can accumulate selectively in tissues of interest and become valuable tools for the diagnosis and therapy of various pathologies. To facilitate the design of targeted NIR imaging agents, it is important to identify simple and affordable fluorescent probes, allowing rapid labelling of biovectors such as proteins, ideally in a site-specific manner. Here, we demonstrate that heptamethine cyanine based fluorophores, such as IR-783, that contain a chloro-cyclohexyl moiety within their polymethine chain can react selectively, at neutral pH, with cysteine residues in proteins to give stable, site-specifically labelled conjugates, that emit in the NIR spectral window. This reaction is exemplified with the labelling of peptides and two protein models: albumin and a Fab' antibody fragment. The resulting fluorescent proteins are stable and suitable for in vivo NIR imaging applications, as shown on a mice model. This straightforward one-step procedure, that does not require the prior derivatisation of the fluorophore with a bioconjugatable handle, should facilitate the production and use of near-infrared labelled proteins in life sciences.
Mots clés
Amino Acid Sequence, Animals, Carbocyanines, chemistry, Cell Line, Tumor, Cysteine, chemistry, Fluorescent Dyes, chemistry, Halogenation, Infrared Rays, Mice, Optical Imaging, Peptides, chemistry, Proteins, chemistry, Staining and Labeling, Tissue Distribution
Référence
Org. Biomol. Chem.. 2018 Nov 9;:
