Introducing affinity and selectivity into galectin-targeting nanoparticles with fluorinated glycan ligands. Issue 3 (24th November 2020)

• Record Type: Journal Article
• Authors: Richards, Sarah-Jane; Keenan, Tessa; Vendeville, Jean-Baptiste; Wheatley, David E.; Chidwick, Harriet; Budhadev, Darshita; Council, Claire E.; Webster, Claire S.; Ledru, Helene; Baker, Alexander N.; Walker, Marc; Galan, M. Carmen; Linclau, Bruno; Fascione, Martin A.; Gibson, Matthew I.
• Is Part Of: Chemical science. Volume 12:Issue 3(2021)
• Page Start: 905
• Page End: 910
• Publication Date: 2020-11-24
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0sc05360k
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : A chemo-enzymatic site-specific fluorination strategy is employed to obtain glyco-nanoparticles with tuneable selectivity towards galectins. Abstract : Galectins are potential biomarkers and therapeutic targets. However, galectins display broad affinity towards β-galactosides meaning glycan-based (nano)biosensors lack the required selectivity and affinity. Using a polymer-stabilized nanoparticle biosensing platform, we herein demonstrate that the specificity of immobilised lacto- N -biose towards galectins can be 'turned on/off' by using site-specific glycan fluorination and in some cases reversal of specificity can be achieved. The panel of fluoro-glycans were obtained by a chemoenzymatic approach, exploiting BiGalK and BiGalHexNAcP enzymes from Bifidobacterium infantis which are shown to tolerate fluorinated glycans, introducing structural diversity which would be very laborious by chemical methods alone. These results demonstrate that integrating non-natural, fluorinated glycans into nanomaterials can encode unprecedented selectivity with potential applications in biosensing.