Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco 915, 5700 San Luis, Argentina.
Bioorg Med Chem. 2010 Jan 1;18(1):158-67. doi: 10.1016/j.bmc.2009.11.009. Epub 2009 Nov 10.
The synthesis, in vitro evaluation, and conformational study of a new series of small-size peptides acting as antifungal agents are reported. In a first step of our study we performed a conformational analysis using Molecular Mechanics calculations. The electronic study was carried out using Molecular electrostatic potentials (MEPs) obtained from RHF/6-31G calculations. On the basis of the theoretical predictions three small-size peptides, RQWKKWWQWRR-NH(2), RQIRRWWQWRR-NH(2), and RQIRRWWQW-NH(2) were synthesized and tested. These peptides displayed a significant antifungal activity against human pathogenic strains including Candida albicans and Cryptococcus neoformans. Our experimental and theoretical results allow the identification of a topographical template which can serve as a guide for the design of new compounds with antifungal properties for potential therapeutic applications against these pathogenic fungi.
报道了一系列新型小分子肽作为抗真菌剂的合成、体外评价和构象研究。在我们研究的第一步中,我们使用分子力学计算进行了构象分析。电子研究使用 RHF/6-31G 计算得到的分子静电势(MEP)进行。基于理论预测,我们合成并测试了三种小分子肽,RQWKKWWQWRR-NH(2)、RQIRRWWQWRR-NH(2)和 RQIRRWWQW-NH(2)。这些肽对包括白色念珠菌和新生隐球菌在内的人类致病菌株表现出显著的抗真菌活性。我们的实验和理论结果确定了一个拓扑模板,可以作为设计具有抗真菌特性的新化合物的指南,用于针对这些致病真菌的潜在治疗应用。