Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376808 | Bioorganic & Medicinal Chemistry Letters | 2008 | 4 Pages |
Abstract
Three typical glycosidase-inhibiting iminoalditols were attached to a polyamine surface displayed on a silicon chip. Exposure to a representative β-glucosidase revealed selective binding events reflecting the different structural features of the inhibitors probed in this study. This provides a proof-of-concept for the successful exploitation of microarrays of typical reversible glycosidase inhibitors of the iminosugar family.
Graphical abstractThe design of an iminoalditol chip and a proof-of-concept study by exposure of the microarray to β-glucosidase from Agrobacterium sp. is reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Andreas J. Steiner, Arnold E. Stütz, Tanja M. Wrodnigg, Chris A. Tarling, Stephen G. Withers, Albin Hermetter, Hannes Schmidinger,