Issue 36, 2024

BODIPYs α-appended with distyryl-linked aryl bisboronic acids: single-step cell staining and turn-on fluorescence binding with d-glucose

Abstract

Small-molecule sensors that are selective for particular sugars are rare. The synthesis of BODIPYs appended with two boronic acid units is reported, alongside cellular staining/labelling and turn-on fluorescence binding data for carbohydrates. The structural frameworks were designed using computational methods, leaning on the chelation characteristics of bis(boronic acids) and the photophysical properties of BODIPYs. Selective binding to glucose is demonstrated via emission and absorption methods, and the challenges of using NMR data for studying carbohydrate binding are discussed. Furthermore, crystal structures, cell permeability and imaging properties of the BODIPYs appended with two boronic acid units are described. This work presents boronic-acid-appended BODIPYs as a potential framework for tunable carbohydrate sensing and chemical biology staining.

Graphical abstract: BODIPYs α-appended with distyryl-linked aryl bisboronic acids: single-step cell staining and turn-on fluorescence binding with d-glucose

Supplementary files

Article information

Article type
Paper
Submitted
17 Jun 2024
Accepted
12 Aug 2024
First published
27 Aug 2024

Org. Biomol. Chem., 2024,22, 7448-7459

BODIPYs α-appended with distyryl-linked aryl bisboronic acids: single-step cell staining and turn-on fluorescence binding with D-glucose

A. Alkaş, J. M. Kofsky, E. C. Sullivan, D. Nebel, K. N. Robertson, C. J. Capicciotti, D. L. Jakeman, E. R. Johnson and A. Thompson, Org. Biomol. Chem., 2024, 22, 7448 DOI: 10.1039/D4OB01013B

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