BODIPYs α-appended with distyryl-linked aryl bisboronic acids: single-step cell staining and turn-on fluorescence binding with D-glucose.
Adil AlkaşJoshua M KofskyEm C SullivanDaisy NebelKatherine N RobertsonChantelle J CapicciottiDavid L JakemanErin R JohnsonAlison ThompsonPublished in: Organic & biomolecular chemistry (2024)
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.
Keyphrases
- small molecule
- high resolution
- single cell
- energy transfer
- cell therapy
- electronic health record
- single molecule
- dna binding
- flow cytometry
- living cells
- magnetic resonance
- blood glucose
- big data
- fluorescent probe
- binding protein
- sensitive detection
- endothelial cells
- stem cells
- type diabetes
- blood pressure
- adipose tissue
- machine learning
- insulin resistance
- bone marrow
- ionic liquid
- artificial intelligence
- data analysis
- climate change
- glycemic control