A nonavalent BODIPY with a multivalent arrangement of α-mannosides enables lectins recognition in fluorescence-based assays

Abstract

We report here on the use of the Tris-BODIPY-OH as a scaffold for the multivalent display of sugar heads. A chloroacetyl thioether ligation reaction easily yields to mannosylated BODIPYs, named Man9-BODIPY and (Man-TEG)9-BODIPY, which display nine mannose residues. Regardless of linker length, both glycoBODIPYs provide an arrangement of mannose heads that allows for proper recognition by the carbohydrate binding domain of Concanavalin A (ConA). Moreover, the interactions of Man9-BODIPY with relevant human lectins, i.e. Dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN) and Langerin, were further investigated. The approach proposed is versatile and paves the way for the development of multivalent and fluorescent glyco-BODIPY probes useful to interrogate carbohydrate-lectin interactions in different biological contexts.

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Article information

Article type
Paper
Submitted
22 Jul 2025
Accepted
28 Nov 2025
First published
05 Dec 2025
This article is Open Access
Creative Commons BY license

RSC Chem. Biol., 2025, Accepted Manuscript

A nonavalent BODIPY with a multivalent arrangement of α-mannosides enables lectins recognition in fluorescence-based assays

E. Purić, G. Biagiotti, J. Tricomi, J. Mravljak, S. Cicchi, M. Laurati, Y. van Kooyk, F. Chiodo, I. Urbancic, M. Anderluh and B. Richichi, RSC Chem. Biol., 2025, Accepted Manuscript , DOI: 10.1039/D5CB00190K

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