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具有形成氢键能力的黄酮类化合物的酚羟基通过使单体 Aβ17-42 的β-折叠构象不稳定来抑制淀粉样成熟纤维。

The role of phenolic OH groups of flavonoid compounds with H-bond formation ability to suppress amyloid mature fibrils by destabilizing β-sheet conformation of monomeric Aβ17-42.

机构信息

Department of Biotechnology, Faculty of Agriculture, Azarbaijan Shahid Madani University, Tabriz, Iran.

Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

PLoS One. 2018 Jun 28;13(6):e0199541. doi: 10.1371/journal.pone.0199541. eCollection 2018.

Abstract

Alzheimer's disease (AD) is a kind of brain disease that arises due to the aggregation and fibrillation of amyloid β-peptides (Aβ). The peptide Aβ17-42 forms U-shape protofilaments of amyloid mature fibrils by cross-β strands, detected in brain cells of individuals with AD. Targeting the structure of Aβ17-42 and destabilizing its β-strands by natural compounds could be effective in the treatment of AD patients. Therefore, the interaction features of monomeric U-shape Aβ17-42 with natural flavonoids including myricetin, morin and flavone at different mole ratios were comprehensively studied to recognize the mechanism of Aβ monomer instability using molecular dynamics (MD) simulations. We found that all flavonoids have tendency to interact and destabilize Aβ peptide structure with mole ratio-dependent effects. The interaction free energies of myricetin (with 6 OHs) and morin (with 5 OHs) were more negative compared to flavone, although the total binding energies of all flavonoids are favorable and negative. Myricetin, morin and flavone penetrated into the core of the Aβ17-42 and formed self-clusters of Aβ17-42-flavonoid complexes. Analysis of Aβ17-42-flavonoids interactions identified that the hydrophobic interactions related to SASA-dependent energy are weak in all complexes. However, the intermolecular H-bonds are a main binding factor for shifting U-shape rod-like state of Aβ17-42 to globular-like disordered state. Myricetin and morin polyphenols form H-bonds with both peptide's carbonyl and amine groups whereas flavone makes H-bonds only with amine substitution. As a result, polyphenols are more efficient in destabilizing β-sheet structures of peptide. Accordingly, the natural polyphenolic flavonoids are useful in forming stable Aβ17-42-flavonoid clusters to inhibit Aβ17-42 aggregation and these compounds could be an effective candidate for therapeutically targeting U-shape protofilaments' monomer in amyloid mature fibrils.

摘要

阿尔茨海默病(AD)是一种由于淀粉样β肽(Aβ)的聚集和纤维化而引起的脑部疾病。肽 Aβ17-42 通过交叉β链形成淀粉样成熟原纤维的 U 形原丝,在 AD 患者的脑细胞中检测到。通过天然化合物靶向 Aβ17-42 的结构并使其β-链不稳定可能对 AD 患者的治疗有效。因此,我们全面研究了单体 U 形 Aβ17-42 与天然类黄酮(包括杨梅素、桑色素和黄酮)在不同摩尔比下的相互作用特征,以使用分子动力学(MD)模拟识别 Aβ 单体不稳定性的机制。我们发现,所有类黄酮都有与 Aβ 肽结构相互作用和去稳定的趋势,具有依赖摩尔比的作用。与黄酮相比,杨梅素(有 6 个 OH)和桑色素(有 5 个 OH)的相互作用自由能更负,尽管所有类黄酮的总结合能都是有利的和负的。杨梅素、桑色素和黄酮渗透到 Aβ17-42 的核心,并形成 Aβ17-42-类黄酮复合物的自聚类。对 Aβ17-42-类黄酮相互作用的分析表明,所有复合物中与 SASA 相关的能量的疏水相互作用都很弱。然而,分子间氢键是将 Aβ17-42 的 U 形棒状状态转移到无规卷曲状态的主要结合因素。杨梅素和桑色素多酚与肽的羰基和胺基都形成氢键,而黄酮仅与胺取代基形成氢键。因此,多酚在使肽的β-折叠结构失稳方面更有效。因此,天然多酚类黄酮可用于形成稳定的 Aβ17-42-类黄酮簇,以抑制 Aβ17-42 聚集,这些化合物可能是针对淀粉样成熟原纤维中 U 形原丝单体的有效治疗候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f386/6023135/045960d9e26a/pone.0199541.g001.jpg

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