Laboratório de Estudos Integrados em Bioquímica Microbiana, Departamento de Microbiologia Geral, Centro de Ciências da Saúde, Instituto de Microbiologia Prof. Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
FEMS Yeast Res. 2010 Mar;10(2):221-4. doi: 10.1111/j.1567-1364.2009.00595.x. Epub 2009 Nov 23.
Secreted aspartyl peptidases (Saps) are virulence attributes produced by Candida albicans that participate in multiple aspects of the fungal biology and pathogenesis. In the present paper, we have shown that amprenavir, a peptidase inhibitor used in HIV chemotherapy, inhibited Sap2 and growth of C. albicans and also promoted ultrastructural alterations. Esterase activity, sterol content, biofilm formation and the expression of surface mannose- and sialic acid-rich glycoconjugates were also reduced by amprenavir.
分泌天冬氨酰肽酶(Saps)是白念珠菌产生的毒力因子,参与真菌生物学和发病机制的多个方面。在本文中,我们表明,蛋白酶抑制剂安普那韦,一种用于 HIV 化疗的药物,抑制了 Sap2 和白念珠菌的生长,同时促进了超微结构的改变。酯酶活性、固醇含量、生物膜形成和表面富含甘露糖和唾液酸的糖缀合物的表达也被安普那韦所降低。