Innovations in Antifungal Drug Discovery among Cell Envelope Synthesis Enzymes through Structural Insights

被引:3
|
作者
Zhou, Yue [1 ]
Reynolds, Todd B. [1 ]
机构
[1] Univ Tennessee, Dept Microbiol, Knoxville, TN 37996 USA
基金
美国国家卫生研究院;
关键词
cryo-EM; structure biology; membrane-bound enzymes; antifungal development; drug resistance; rational drug design; INOSITOL PHOSPHORYLCERAMIDE SYNTHASE; PHOSPHATIDYLSERINE DECARBOXYLASE ACTIVITY; IN-VITRO ACTIVITY; SACCHAROMYCES-CEREVISIAE; CANDIDA-ALBICANS; SERINE PALMITOYLTRANSFERASE; SPHINGOLIPID SYNTHESIS; SQUALENE SYNTHASE; CERAMIDE SYNTHASE; YEAST MUTANT;
D O I
10.3390/jof10030171
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Life-threatening systemic fungal infections occur in immunocompromised patients at an alarming rate. Current antifungal therapies face challenges like drug resistance and patient toxicity, emphasizing the need for new treatments. Membrane-bound enzymes account for a large proportion of current and potential antifungal targets, especially ones that contribute to cell wall and cell membrane biosynthesis. Moreover, structural biology has led to a better understanding of the mechanisms by which these enzymes synthesize their products, as well as the mechanism of action for some antifungals. This review summarizes the structures of several current and potential membrane-bound antifungal targets involved in cell wall and cell membrane biosynthesis and their interactions with known inhibitors or drugs. The proposed mechanisms of action for some molecules, gleaned from detailed inhibitor-protein studeis, are also described, which aids in further rational drug design. Furthermore, some potential membrane-bound antifungal targets with known inhibitors that lack solved structures are discussed, as these might be good enzymes for future structure interrogation.
引用
收藏
页数:33
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