Oli Swarna, Abdelmohsen Usama Ramadan, Hentschel Ute, Schirmeister Tanja
Institute of Pharmacy and Biochemistry, Johannes Gutenberg-University of Mainz, Staudinger Weg 5, Mainz 55128, Germany.
Department of Botany II, Julius-von-Sachs-Institute for Biological Sciences, University of Würzburg, Julius-von-Sachs Platz 3, Würzburg 97082, Germany.
Mar Drugs. 2014 May 2;12(5):2614-22. doi: 10.3390/md12052614.
In this paper, we report new protease inhibitory activity of plakortide E towards cathepsins and cathepsin-like parasitic proteases. We further report on its anti-parasitic activity against Trypanosoma brucei with an IC₅₀ value of 5 μM and without cytotoxic effects against J774.1 macrophages at 100 μM concentration. Plakortide E was isolated from the sponge Plakortis halichondroides using enzyme assay-guided fractionation and identified by NMR spectroscopy and mass spectrometry. Furthermore, enzyme kinetic studies confirmed plakortide E as a non-competitive, slowly-binding, reversible inhibitor of rhodesain.
在本文中,我们报道了软海绵素E对组织蛋白酶和类组织蛋白酶寄生虫蛋白酶的新的蛋白酶抑制活性。我们还进一步报道了其对布氏锥虫的抗寄生虫活性,IC₅₀值为5 μM,且在100 μM浓度下对J774.1巨噬细胞无细胞毒性作用。软海绵素E是通过酶分析导向分级分离从海绵Halichondroides中分离得到的,并通过核磁共振光谱和质谱进行鉴定。此外,酶动力学研究证实软海绵素E是罗德西亚锥虫蛋白酶的非竞争性、缓慢结合、可逆抑制剂。