PubAg

Main content area

Chemoenzymatic synthesis of GDP-L-fucose and the Lewis X glycan derivatives

Author:
Wang, Wei, Hu, Tianshun, Frantom, Patrick A., Zheng, Tianqing, Gerwe, Brian, del Amo, David Soriano, Garret, Sarah, Seidel, Ronald D. III., Wu, Peng
Source:
Proceedings of the National Academy of Sciences of the United States of America 2009 v.106 no.38 pp. 16096-16101
ISSN:
0027-8424
Subject:
Bacteroides fragilis, Helicobacter pylori, cost effectiveness, epitopes, fucose, polysaccharides, trisaccharides
Abstract:
Lewis X (Lex)-containing glycans play important roles in numerous cellular processes. However, the absence of robust, facile, and cost-effective methods for the synthesis of Lex and its structurally related analogs has severely hampered the elucidation of the specific functions of these glycan epitopes. Here we demonstrate that chemically defined guanidine 5'-diphosphate-β-L-fucose (GDP-fucose), the universal fucosyl donor, the Lex trisaccharide, and their C-5 substituted derivatives can be synthesized on preparative scales, using a chemoenzymatic approach. This method exploits L-fucokinase/GDP-fucose pyrophosphorylase (FKP), a bifunctional enzyme isolated from Bacteroides fragilis 9343, which converts L-fucose into GDP-fucose via a fucose-1-phosphate (Fuc-1-P) intermediate. Combining the activities of FKP and a Helicobacter pylori α1,3 fucosyltransferase, we prepared a library of Lex trisaccharide glycans bearing a wide variety of functional groups at the fucose C-5 position. These neoglycoconjugates will be invaluable tools for studying Lex-mediated biological processes.
Agid:
2366112