Inhibition of S. aureus α-hemolysin and B. anthracis lethal toxin by β-cyclodextrin derivatives
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- 作者：Vladimir A. Karginov ; Ekaterina M. Nestorovich ; Frank Schmidtmann ; Tanisha M. Robinson ; Adiamseged Yohannes ; Nour Eddine Fahmi ; Sergey M. Bezrukov ; Sidney M. Hecht
- 关键词：Anthrax toxin ; α ; -Hemolysin ; Staphylococcus aureus ; Inhibitors ; β ; -Cyclodextrin derivatives
- 刊名：Bioorganic and Medicinal Chemistry
- 出版年：2007
- 出版时间：15 August 2007
- 年：2007
- 卷：15
- 期：16
- 页码：5424-5431
- 全文大小：1852 K
文摘
Many pathogens utilize the formation of transmembrane pores in target cells in the process of infection. A great number of pore-forming proteins, both bacterial and viral, are considered to be important virulence factors, which makes them attractive targets for the discovery of new therapeutic agents. Our research is based on the idea that compounds designed to block the pores can inhibit the action of virulence factors, and that the chances to find high affinity blocking agents increase if they have the same symmetry as the target pore. Recently, we demonstrated that derivatives of β-cyclodextrin inhibited anthrax lethal toxin (LeTx) action by blocking the transmembrane pore formed by the protective antigen (PA) subunit of the toxin. To test the broader applicability of this approach, we sought β-cyclodextrin derivatives capable of inhibiting the activity of Staphylococcus aureus α-hemolysin (α-HL), which is regarded as a major virulence factor playing an important role in staphylococcal infection. We identified several amino acid derivatives of β-cyclodextrin that inhibited the activity of α-HL and LeTx in cell-based assays at low micromolar concentrations. One of the compounds was tested for the ability to block ion conductance through the pores formed by α-HL and PA in artificial lipid membranes. We anticipate that this approach can serve as the basis for a structure-directed drug discovery program to find new and effective therapeutics against various pathogens that utilize pore-forming proteins as virulence factors.