流出
抗药性
唑
生物
抗真菌药
多重耐药
抗真菌药
药品
药理学
药物发现
抗真菌
微生物学
化学
生物化学
作者
Ann R. Holmes,Tony S. Cardno,J. Jacob Strouse,Irena Ivnitski‐Steele,Mikhail V. Keniya,Kurt Lackovic,Brian C. Monk,Larry A. Sklar,Richard D. Cannon
标识
DOI:10.4155/fmc-2016-0050
摘要
Resistance to antifungal drugs is an increasingly significant clinical problem. The most common antifungal resistance encountered is efflux pump-mediated resistance of Candida species to azole drugs. One approach to overcome this resistance is to inhibit the pumps and chemosensitize resistant strains to azole drugs. Drug discovery targeting fungal efflux pumps could thus result in the development of azole-enhancing combination therapy. Heterologous expression of fungal efflux pumps in Saccharomyces cerevisiae provides a versatile system for screening for pump inhibitors. Fungal efflux pumps transport a range of xenobiotics including fluorescent compounds. This enables the use of fluorescence-based detection, as well as growth inhibition assays, in screens to discover compounds targeting efflux-mediated antifungal drug resistance. A variety of medium- and high-throughput screens have been used to identify a number of chemical entities that inhibit fungal efflux pumps.
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