Masman Marcelo F, Rodríguez Ana M, Raimondi Marcela, Zacchino Susana A, Luiten Paul G M, Somlai Csaba, Kortvelyesi Tamas, Penke Botond, Enriz Ricardo D
Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco 915, 5700 San Luis, Argentina.
Eur J Med Chem. 2009 Jan;44(1):212-28. doi: 10.1016/j.ejmech.2008.02.019. Epub 2008 Feb 29.
The synthesis, in vitro evaluation, and conformational study of RQIKIWFQNRRMKWKK-NH(2) (penetratin) and related derivatives acting as antifungal agents are reported. Penetratin and some of its derivatives displayed antifungal activity against the human opportunistic pathogenic standardized ATCC strains Candida albicans and Cryptococcus neoformans as well as clinical isolates of C. neoformans. Among the compounds tested, penetratin along with the nonapeptide RKWRRKWKK-NH(2) and the tetrapeptide RQKK-NH(2) exhibited significant antifungal activities against the Cryptococcus species. A comprehensive conformational analysis on the peptides reported here using three different approaches, molecular mechanics, simulated annealing and molecular dynamics simulations, was carried out. The experimental and theoretical results allow us to identify a topographical template which may provide a guide for the design of new compounds with antifungal characteristics against C. neoformans.
本文报道了作为抗真菌剂的RQIKIWFQNRRMKWKK-NH(2)(穿膜肽)及其相关衍生物的合成、体外评估和构象研究。穿膜肽及其一些衍生物对人类机会致病性标准ATCC菌株白色念珠菌和新型隐球菌以及新型隐球菌临床分离株具有抗真菌活性。在所测试的化合物中,穿膜肽与九肽RKWRRKWKK-NH(2)和四肽RQKK-NH(2)对隐球菌属表现出显著的抗真菌活性。本文使用分子力学、模拟退火和分子动力学模拟三种不同方法对这些肽进行了全面的构象分析。实验和理论结果使我们能够确定一个拓扑模板,可为设计针对新型隐球菌具有抗真菌特性的新化合物提供指导。