Single-molecule determination of the isomers of D-glucose and D-fructose that bind to boronic acids

Journal article

Monosaccharides, such as D-glucose and D-fructose, exist in aqueous solution as an equilibrium mixture of cyclic isomers and can be detected with boronic acids by the reversible formation of boronate esters. The engineering of accurate, discriminating and continuous monitoring devices relies on knowledge of which cyclic isomer of a sugar binds to a boronic acid receptor. Here, by monitoring fluctuations in ionic current, we show that an engineered α-hemolysin (αHL) nanopore modified with a boronic acid reacts reversibly with D-glucose as the pyranose isomer (α-D-glucopyranose) and D-fructose as either the furanose (β-D-fructofuranose) or the pyranose (β-D fructopyranose). Both of these binding modes contradict current binding models. With this knowledge, we distinguished the individual sugars in a mixture of D-maltose, D-glucose and D-fructose.

Authors: Ramsay, W; Bayley, H

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Wiley
• Journal: Angewandte Chemie International Edition
• Volume: 57
• Issue: 11
• Pages: 2841–2845
• Publication date: 2018-01-24
• Acceptance date: 2018-01-23
• DOI: 10.1002/anie.201712740
• EISSN: 1521-3773
• ISSN: 1433-7851
• Pmid: 29365215
• Language: English
• Keywords: nanoreactor; alpha-hemolysin; boronic acid; single-molecule; sugar detection