MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, School of Physics, Xi'an Jiaotong University, Xi'an 710049, China.
State Key Laboratory of Surface Physics, Department of Physics, Fudan University, 2005 Songhu Road, Shanghai 200438, China.
Int J Mol Sci. 2024 Jan 29;25(3):1636. doi: 10.3390/ijms25031636.
Alzheimer's disease and Type 2 diabetes are two epidemiologically linked diseases which are closely associated with the misfolding and aggregation of amyloid proteins amyloid-β (Aβ) and human islet amyloid polypeptide (hIAPP), respectively. The co-aggregation of the two amyloid proteins is regarded as the fundamental molecular mechanism underlying their pathological association. The green tea extract epigallocatechin-3-gallate (EGCG) has been extensively demonstrated to inhibit the amyloid aggregation of Aβ and hIAPP proteins. However, its potential role in amyloid co-aggregation has not been thoroughly investigated. In this study, we employed the enhanced-sampling replica exchange molecular dynamics simulation (REMD) method to investigate the effect of EGCG on the co-aggregation of Aβ and hIAPP. We found that EGCG molecules substantially diminish the β-sheet structures within the amyloid core regions of Aβ and hIAPP in their co-aggregates. Through hydrogen-bond, π-π and cation-π interactions targeting polar and aromatic residues of Aβ and hIAPP, EGCG effectively attenuates both inter-chain and intra-chain interactions within the co-aggregates. All these findings indicated that EGCG can effectively inhibit the co-aggregation of Aβ and hIAPP. Our study expands the potential applications of EGCG as an anti-amyloidosis agent and provides therapeutic options for the pathological association of amyloid misfolding disorders.
阿尔茨海默病和 2 型糖尿病是两种在流行病学上相关的疾病,分别与淀粉样蛋白β(Aβ)和人胰岛淀粉样多肽(hIAPP)的错误折叠和聚集密切相关。两种淀粉样蛋白的共聚集被认为是它们病理关联的基本分子机制。绿茶提取物表没食子儿茶素没食子酸酯(EGCG)已被广泛证明可抑制 Aβ和 hIAPP 蛋白的淀粉样聚集。然而,其在淀粉样共聚集中的潜在作用尚未得到彻底研究。在这项研究中,我们采用增强采样 replica 交换分子动力学模拟(REMD)方法研究了 EGCG 对 Aβ和 hIAPP 共聚集的影响。我们发现,EGCG 分子显著减少了 Aβ和 hIAPP 共聚集物中淀粉样核心区域内的β-折叠结构。通过氢键、π-π 和阳离子-π 相互作用靶向 Aβ和 hIAPP 的极性和芳香残基,EGCG 有效地减弱了共聚集物内的链间和链内相互作用。所有这些发现表明,EGCG 可以有效地抑制 Aβ和 hIAPP 的共聚集。我们的研究扩展了 EGCG 作为抗淀粉样变性剂的潜在应用,并为淀粉样蛋白错误折叠疾病的病理关联提供了治疗选择。