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在阿尔茨海默病框架下,多胺缀合作为一种靶向淀粉样蛋白聚集的有前景策略。

Polyamine Conjugation as a Promising Strategy To Target Amyloid Aggregation in the Framework of Alzheimer's Disease.

作者信息

Simoni Elena, Caporaso Roberta, Bergamini Christian, Fiori Jessica, Fato Romana, Miszta Przemyslaw, Filipek Sławomir, Caraci Filippo, Giuffrida Maria Laura, Andrisano Vincenza, Minarini Anna, Bartolini Manuela, Rosini Michela

机构信息

Department of Pharmacy & Biotechnology, Alma Mater Studiorum-University of Bologna , Via Belmeloro 6, 40126 Bologna, Italy.

Faculty of Chemistry, Biological & Chemical Research Centre University of Warsaw , Pasteura 1, 02093 Warsaw, Poland.

出版信息

ACS Med Chem Lett. 2016 Sep 26;7(12):1145-1150. doi: 10.1021/acsmedchemlett.6b00339. eCollection 2016 Dec 8.

Abstract

Spermine conjugates -, carrying variously decorated 3,5-dibenzylidenepiperidin-4-one as bioactive motives, were designed to direct antiaggregating properties into mitochondria, using a polyamine functionality as the vehicle tool. The study confirmed mitochondrial import of the catechol derivative , which displayed effective antiaggregating activity and neuroprotective effects against Aβ-induced toxicity. Notably, a key functional role for the polyamine motif in Aβ molecular recognition was also unraveled. This experimental readout, which was supported by in silico studies, gives important new insight into the polyamine's action. Hence, we propose polyamine conjugation as a promising strategy for the development of neuroprotectant leads that may contribute to decipher the complex picture of Aβ toxicity.

摘要

精胺共轭物——携带各种修饰的3,5-二亚苄基哌啶-4-酮作为生物活性基团,旨在利用多胺功能作为载体工具,将抗聚集特性导向线粒体。该研究证实了儿茶酚衍生物的线粒体导入,其显示出有效的抗聚集活性以及对Aβ诱导毒性的神经保护作用。值得注意的是,还揭示了多胺基序在Aβ分子识别中的关键功能作用。这一实验结果得到了计算机模拟研究的支持,为多胺的作用提供了重要的新见解。因此,我们提出多胺共轭作为一种有前景的策略,用于开发可能有助于解读Aβ毒性复杂情况的神经保护先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe6d/5150688/a3b1e25cc443/ml-2016-00339w_0001.jpg

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