The decasaccharide sialyl-trimeric-Lewis x is a component of glycoproteins and glycolipids that serve as E-and P-selectin ligands. The synthesis of this target structure was accomplished by utilizing a combination of chemical and enzymatic methods. Highlights of the chemical synthesis include minima
Chemoenzymatic synthesis of GM3, Lewis x and sialyl Lewis x oligosaccharides in 13C-enriched form
β Scribed by Mark A. Probert; Mark.J. Milton; Richard Harris; Sergio Schenkman; Jonathan M. Brown; Steven W. Homans; Robert A. Field
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 251 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
In connection with studies on the solution and protein-bound conformation of oligosaecharides, we had reason to consider the application of 13C-enriched sugars. Herein we describe the synthesis of ganglioside GM3 trisaccharide (1), Lewis x trisaccharide (2) and the sialyl Lewis x tetrasaccharide (3) from [U-13C]-D-GIc, [U-I 3C] -L-Gal and [U-13C]-pymvate.
π SIMILAR VOLUMES
Sialyl Lewis x (sLe x ) derivatives conjugated to readily visualized molecular labels are useful chemical probes to study selectin Β± carbohydrate interactions. Localization of the selectins on the surface of leukocytes and activated endothelial cells can be detected through fluorescence of bound sel