| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1929340 | Biochemical and Biophysical Research Communications | 2012 | 6 Pages |
A series of 12 carbohydrate compounds were synthesized by introduction of a sulfated group at specific positions and evaluated for their activities against dengue virus (DENV) infection as well as binding to BHK-21 cells. 3-O-sulfated GlcA was active against DENV infection, whereas 2-O-sulfated GlcA and 3,6-di-O-sulfated Glc showed negligible activity. Persulfated compounds did not inhibit DENV infection. These results provided a rationale for designing sulfated carbohydrate compounds with low molecular mass as anti-DENV agents targeting E protein functions. 3-O-Sulfated GlcA showed no significant cytotoxicity at 1 mM. The EC50 value (120 μM) was lower than that of sucrose octasulfate (SOS), a small molecular weight inhibitor of DENV infection. Two negatively charged groups, 3-O-sulfate and 6-C-carboxylic acid, appear to be essential for anti-DENV activity. We performed docking study to investigate the binding potential of 3-O-sulfated GlcA with respect to DENV E protein. The docking study showed that distance and conformation of these negative charges on the carbohydrate may be suitable for association with three amino acid residues of E protein critically involved in virus adsorption (Lys295, Ser145, and Gly159). This interaction may competitively prevent functional DENV binding to receptor(s) on host cells. In conclusion, 3-O-sulfated GlcA is a chemical probe that may facilitate exploration of the molecular mechanisms underlying manifestations of dengue diseases.
► Sulfated carbohydrates were synthesized and evaluated for anti-dengue virus activity. ► The EC50 value of methyl 3-O-sulfated α-GlcA was 120 μM against DENV infection. ► Methyl 3-O-sulfated α-GlcA showed no significant cytotoxicity at 1 mM. ► 3-O-sulfate and 6-C-carboxylic acid groups may be essential for anti-DENV activity.
