Hidari Kazuya I P J, Takahashi Naonori, Arihara Masataka, Nagaoka Masato, Morita Koichi, Suzuki Takashi
Department of Biochemistry, University of Shizuoka, School of Pharmaceutical Sciences, Global COE Program for Innovation in Human Health Sciences, 52-1 Yada, Suruga-ku, Shizuoka-shi, Shizuoka 422-8526, Japan.
Biochem Biophys Res Commun. 2008 Nov 7;376(1):91-5. doi: 10.1016/j.bbrc.2008.08.100. Epub 2008 Aug 30.
A sulfated polysaccharide, named fucoidan, from the marine alga Cladosiphon okamuranus is comprised of carbohydrate units containing glucuronic acid and sulfated fucose residues. Here we found this compound potently inhibits dengue virus type 2 (DEN2) infection. Viral infection was inhibited when DEN2, but not other serotypes, was pretreated with fucoidan. A carboxy-reduced fucoidan derivative in which glucuronic acid was converted to glucose did not inhibit viral infection. Elimination of the sulfated function group from fucoidan significantly attenuated the inhibitory activity on DEN2 infection with <1% fucoidan. DEN2 particles bound exclusively to fucoidan, indicating that fucoidan interacts directly with envelope glycoprotein (EGP) on DEN2. Structure-based analysis suggested that Arg323 of DEN2 EGP, which is conformationally proximal to one of the putative heparin binding residues, Lys310, is critical for the interaction with fucoidan. In conclusion, both the sulfated group and glucuronic acid of fucoidan account for the inhibition of DEN2 infection.
一种名为岩藻依聚糖的硫酸化多糖,来源于海洋藻类冈村枝管藻,由含有葡萄糖醛酸和硫酸化岩藻糖残基的碳水化合物单元组成。在此,我们发现该化合物能有效抑制2型登革病毒(DEN2)感染。当用岩藻依聚糖预处理DEN2(而非其他血清型)时,病毒感染受到抑制。一种羧基还原的岩藻依聚糖衍生物,其中葡萄糖醛酸已转化为葡萄糖,并未抑制病毒感染。从岩藻依聚糖中去除硫酸化官能团,显著减弱了对DEN2感染的抑制活性,<1%的岩藻依聚糖时抑制活性大幅降低。DEN2颗粒仅与岩藻依聚糖结合,表明岩藻依聚糖直接与DEN2上的包膜糖蛋白(EGP)相互作用。基于结构的分析表明,DEN2 EGP的Arg323与假定的肝素结合残基之一Lys310在构象上相近,对与岩藻依聚糖的相互作用至关重要。总之,岩藻依聚糖的硫酸化基团和葡萄糖醛酸均对DEN2感染的抑制起作用。