School of Chemistry (F11), The University of Sydney, 2006, Sydney, NSW, Australia.
Department of Pathology and Experimental Therapeutics, Cancer Cell Biology Research Group, University of Barcelona, Barcelona, Spain.
Sci Rep. 2017 Aug 24;7(1):9397. doi: 10.1038/s41598-017-09645-9.
Prodigiosin is one of the most potent anion transporters in lipid bilayer membranes reported to date. Inspired by the structure of this natural product, we have recently designed and synthesised a new class of H/Cl cotransporters named 'perenosins'. Here we report a new library of indole-based perenosins and their anion transport properties. The new transporters demonstrated superior transmembrane transport efficiency when compared to other indole-based transporters, due to favourable encapsulating effects from the substituents on the perenosin backbone. Anion transport assays were used to determine the mechanism of chloride transport revealing that the compounds function as 'strict' HCl cotransporters. Cell viability studies showed that some compounds specifically trigger late-onset cell death after 72 h with a unique correlation to the position of alkyl chains on the perenosins. Further investigations of cell death mechanism showed a mixture of cell cycle arrest and apoptosis was responsible for the observed decrease in cell viability.
灵菌红素是迄今为止报道的脂质双分子层膜中最有效的阴离子转运体之一。受该天然产物结构的启发,我们最近设计并合成了一类新型的 H/Cl 共转运体,名为“佩罗尼辛”。在这里,我们报告了一系列新的吲哚型佩罗尼辛及其阴离子转运特性。与其他基于吲哚的转运体相比,由于佩罗尼辛主链上取代基的有利包封作用,这些新的转运体表现出更高的跨膜转运效率。阴离子转运实验用于确定氯化物转运的机制,结果表明这些化合物作为“严格”的 HCl 共转运体发挥作用。细胞活力研究表明,一些化合物在 72 小时后会特异性地触发迟发性细胞死亡,这与佩罗尼辛上烷基链的位置有独特的相关性。对细胞死亡机制的进一步研究表明,细胞周期停滞和细胞凋亡的混合物是导致细胞活力下降的原因。