From Naturally-Sourced Protease Inhibitors to New Treatments for Fungal Infections

被引:21
作者
Gutierrez-Gongora, Davier [1 ,2 ]
Geddes-McAlister, Jennifer [1 ,3 ]
机构
[1] Univ Guelph, Dept Mol & Cellular Biol, Guelph, ON N1G 2W1, Canada
[2] Univ La Habana, Fac Biol, Ctr Estudio Prot, Havana 10400, Cuba
[3] Canadian Prote & Artificial Intelligence Res & Tr, Guelph, ON N1G 2W1, Canada
基金
加拿大创新基金会; 加拿大健康研究院;
关键词
proteases; protease inhibitors; fungal pathogens; natural compounds; biomedical applications; antimicrobial resistance; CANDIDA-ALBICANS; SERINE-PROTEASE; TRYPSIN-INHIBITOR; PROTEOLYTIC-ENZYMES; HIV-1; PROTEASE; CRYPTOCOCCUS-NEOFORMANS; ANTIMICROBIAL ACTIVITY; PROTEINASE-INHIBITOR; ANTIFUNGAL ACTIVITY; CRYSTAL-STRUCTURE;
D O I
10.3390/jof7121016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Proteases are involved in a broad range of physiological processes, including host invasion by fungal pathogens, and enzymatic inhibition is a key molecular mechanism controlling proteolytic activity. Importantly, inhibitors from natural or synthetic sources have demonstrated applications in biochemistry, biotechnology, and biomedicine. However, the need to discover new reservoirs of these inhibitory molecules with improved efficacy and target range has been underscored by recent protease characterization related to infection and antimicrobial resistance. In this regard, naturally-sourced inhibitors show promise for application in diverse biological systems due to high stability at physiological conditions and low cytotoxicity. Moreover, natural sources (e.g., plants, invertebrates, and microbes) provide a large reservoir of undiscovered and/or uncharacterized bioactive molecules involved in host defense against predators and pathogens. In this Review, we highlight discoveries of protease inhibitors from environmental sources, propose new opportunities for assessment of antifungal activity, and discuss novel applications to combat biomedically-relevant fungal diseases with in vivo and clinical purpose.
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页数:13
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