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首页> 外文期刊>Natural product research >Continental and Antarctic Lichens: isolation, identification and molecular modeling of the depside tenuiorin from the Antarctic lichen Umbilicaria antarctica as tau protein inhibitor
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Continental and Antarctic Lichens: isolation, identification and molecular modeling of the depside tenuiorin from the Antarctic lichen Umbilicaria antarctica as tau protein inhibitor

机译:大陆和南极地衣:从南极地衣Umbilicaria南极洲作为Tau蛋白抑制剂的分离,鉴定和分子建模

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摘要

Alzheimer's disease (AD) is the most common form of dementia involving A beta and tau protein. So far, AD cure remains elusive, but considering that AD progresses throughout tau pathology, which turns tau protein an appropriate target, besides tau is also included in other neurodegenerative disorders named as tauopathies. Here, we have isolated seventeen compounds belonging to six lichens species. Due to scarce of spectroscopic data of the compound 5,7-dihydroxy-6-methylphthalide, we explained their structural elucidation based on NMR data. In this study, we show that only tenuiorin from Umbilicaria antarctica inhibited 50% of tau 4R at 100 mu M. Then, we shown that molecular interactions of tenuiorin with the steric zipper model of the hexapeptide (306)VQIVYK(311) were studied by docking calculations and the results suggested that tenuiorin forms both hydrogen bonds with lysine and glutamine side chains and forms several hydrophobic interactions with valine and lysine from (306)VQIVYK(311) motif.
机译:阿尔茨海默病(AD)是最常见的痴呆形式,涉及β和TAU蛋白。到目前为止,广告治愈仍然难以捉摸,但考虑到广告在整个Tau病理学中进展,其转动Tau蛋白的适当靶标,除了TAU也包括在其他名为TauOxates的神经变性障碍之外。在这里,我们已经孤立了属于六种地衣物种的十七种化合物。由于化合物5,7-二羟基-6-甲基酞的光谱数据稀缺,我们解释了基于NMR数据的结构阐明。在这项研究中,我们表明,只有来自Umbilicaria抗野生的TRAUIORIN抑制了50%的TAU 4R在100 mu M.然后,通过研究了与六肽的空间拉链模型(306)VQivyk(311)的子管素的分子相互作用对接计算和结果表明,Tenuiorin与赖氨酸和谷氨酰胺侧链形成氢键,并形成来自(306)Vqivyk(311)基序的缬氨酸和赖氨酸的几种疏水相互作用。

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