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

被引:0
作者
Alkas, Adil [1 ]
Kofsky, Joshua M. [2 ]
Sullivan, Em C. [1 ]
Nebel, Daisy [2 ]
Robertson, Katherine N. [3 ]
Capicciotti, Chantelle J. [2 ]
Jakeman, David L. [1 ,4 ]
Johnson, Erin R. [1 ]
Thompson, Alison [1 ]
机构
[1] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4J3, Canada
[2] Queens Univ, Dept Chem, Dept Biomed & Mol Sci, Dept Surg, Kingston, ON K7L 3N6, Canada
[3] St Marys Univ, Dept Chem, Halifax, NS B3H 3C3, Canada
[4] Dalhousie Univ, Coll Pharm, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
FUNCTIONALIZED BORON-DIPYRROMETHENE; SENSORS; DEPROTECTION; RECOGNITION; PROBES; DYES; DERIVATIVES; COMPLEXES; FURANOSE; PLATFORM;
D O I
10.1039/d4ob01013b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
收藏
页码:7448 / 7459
页数:12
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