Glycosylphosphatidylinositols Are Potential Targets for the Development of Novel Inhibitors for Aerolysin-Type of Pore-Forming Bacterial Toxins

被引:13
|
作者
Wu, Qiuye [2 ]
Guo, Zhongwu [1 ]
机构
[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA
[2] Second Mil Med Univ, Sch Pharm, Shanghai 200433, Peoples R China
基金
美国国家科学基金会;
关键词
GPI; carbohydrate; glycolipid; pore-forming toxin; toxin inhibitor; aerolysin; CELL-SURFACE GLYCANS; PHOSPHATIDYLINOSITOL GPI ANCHOR; SEPTICUM ALPHA-TOXIN; AGALACTIAE CAMP FACTOR; GLYCOBIOSYL PHOSPHATIDYLINOSITOL; CONVERGENT SYNTHESIS; TRYPANOSOMA-BRUCEI; MEMBRANE-CHANNEL; RECEPTOR-BINDING; PROTEIN;
D O I
10.1002/med.20167
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Many bacteria produce toxins that cause damage through the formation of pores in the host cell membrane. Some of these toxins, such as aerolysin, use glycosylphosphatidylinositols (GPIS) as their binding receptors to assist the pore formation on the host cell surface and the subsequent insertion of the resultant pores into the cell membrane. GPIs are a class of complex glycolipids that anchor surface proteins and glycoproteins onto the cell membrane in eukaryotic species. This review has summarized the reported evidences supporting the GPI-dependent pore-forming mechanism for aerolysin-type of toxins and analyzed the possibility of targeting this unique process for the design and development of novel GPI-based inhibitors for these pore-forming bacterial toxins. (C) 2009 Wiley Periodicals, Inc. Med Res Rev, 30, No. 2. 258-269, 2010
引用
收藏
页码:258 / 269
页数:12
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