Wang Tao, Liu Xiao-Huan, Wu Mian-Bin, Ge Shun
School of Biological Science, Jining Medical University, Jining, China.
Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, China.
J Mol Model. 2018 Apr 26;24(5):118. doi: 10.1007/s00894-018-3645-4.
Bacilysin is one of the simplest antimicrobial peptides and has drawn great attention for its excellent performance against Candida albicans. In this study, the antifungal mechanism of bacilysin was investigated. The target enzyme glucosamine-6-phosphate synthase (GFA) was expressed heterologously in Escherichia coli and its inhibition by bacilysin and derivatives was studied. It was concluded that bacilysin could be hydrolyzed by a proteinase of C. albicans, and that the released product, anticapsin, then inhibited the aminotransferase activity of GFA. This result was verified by molecular simulation, and the interaction mode of anticapsin with GFA was detailed, which provides data for the development of novel antifungal drugs. Transport of bacilysin into fungal cells was also simulated and it was shown that bacilysin is more readily transported into cells than anticapsin. Thus, our findings support a mechanism whereby bacilysin is transported into fungal pathogens, hydrolyzed to anticapsin, which then inhibits GFA.
杆菌溶素是最简单的抗菌肽之一,因其对白色念珠菌的优异抗菌性能而备受关注。在本研究中,对杆菌溶素的抗真菌机制进行了研究。靶标酶6-磷酸葡糖胺合酶(GFA)在大肠杆菌中进行了异源表达,并研究了杆菌溶素及其衍生物对它的抑制作用。得出的结论是,杆菌溶素可被白色念珠菌的一种蛋白酶水解,释放出的产物抗荚膜素随后抑制GFA的转氨酶活性。该结果通过分子模拟得到了验证,并详细阐述了抗荚膜素与GFA的相互作用模式,为新型抗真菌药物的开发提供了数据。还模拟了杆菌溶素进入真菌细胞的过程,结果表明杆菌溶素比抗荚膜素更容易进入细胞。因此,我们的研究结果支持了一种机制,即杆菌溶素被转运到真菌病原体中,水解为抗荚膜素,然后抗荚膜素抑制GFA。