对阿尔茨海默氏症和 SARS-CoV 神经变性过程中 APOE4、NLRP3 和 ACE2-SPIKE 复合物之间相互作用的分子内建模:对了解发病机制和制定治疗策略的意义。

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biomolecular Structure & Dynamics Pub Date : 2024-11-01 Epub Date: 2023-08-29 DOI:10.1080/07391102.2023.2252094
Sriranjini A S, Ashish Thapliyal, Kumud Pant
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引用次数: 0

摘要

包括阿尔茨海默病(AD)在内的神经退行性病变与毒性极强的严重急性呼吸系统综合征冠状病毒(SARS-CoV)之间的多方面相互作用牵涉到多种疾病。AD 和 SARS-CoV 的发病机制涉及 APOE4 等位基因、NLRP3 炎性体和 ACE2-SPIKE 复合物。APOE4 是 APOE 基因的一种遗传多态性,与 AD 易感性增加有关。NLRP3 是先天性免疫系统的一种炎症蛋白,在免疫反应级联中起着关键作用。在 SARS-CoV 中,ACE2 受体是进入细胞的主要通道,而 APOE4 则与 ACE2-尖峰蛋白复合物发生复杂的相互作用,从而增强病毒的内化过程。NLRP3 与 ACE2-尖峰蛋白复合物的相互作用导致炎症信号增强。APOE4/NLRP3与ACE2-尖峰蛋白复合物相互作用的趋同性表明,SARS与AD之间可能存在联系。因此,目前的研究利用 SARS-CoV 数据集集中研究两者之间的关联,探索 SARS-CoV 和 AD 发病机制的可能机制。研究还进一步扩展到利用分子动力学模拟技术揭示 APOE4 和 NLRP3 与 ACE2-Spike 蛋白复合物在分子水平上的相互作用。通过评估 Chyawanprash 保健食品对 APOE4-ACE2-Spike 蛋白和 NLRP3-ACE2-Spike 蛋白复合物的抑制潜力,评估了其治疗功效。值得注意的是,我们的模拟结果清楚地表明,在整个模拟期间,化合物 Phyllantidine 与目标复合物的结合能力强大而持久。研究结果进一步证实了 APOE4 和 NLRP3 是导致 SARS-CoV 和 AD 发病的主要假说。因此,这项研究为理解 AD 和 SARS-CoV 之间复杂的相互作用建立了一个范例,并为这一领域的进一步研究奠定了基础。
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In-silico modeling of the interplay between APOE4, NLRP3, and ACE2-SPIKE complex in neurodegeneration between Alzheimer and SARS-CoV: implications for understanding pathogenesis and developing therapeutic strategies.

The multifaceted interplay between neurodegenerative pathologies, including Alzheimer's disease (AD), and the highly virulent severe acute respiratory syndrome coronavirus (SARS-CoV), is implicated in various conditions. AD and SARS-CoV pathogenesis involve the APOE4 allele, NLRP3 inflammasome, and ACE2-SPIKE complex. APOE4, a genetic polymorphism of the APOE gene, is associated with an increased susceptibility to AD. NLRP3, an inflammatory protein of the innate immune system, plays a pivotal role in immune response cascades. In SARS-CoV, the ACE2 receptor serves as the principal portal for cellular entry, while APOE4 intricately interacts with the ACE2-spike protein complex, enhancing viral internalization process. The interaction of NLRP3 with the ACE2-spike protein complex leads to increased inflammatory signaling. The convergence of APOE4/NLRP3 and ACE2-spike protein complex interactions suggests a possible link between SARS and AD. Therefore, the current research centralizes the association between by utilizing SARS-CoV datasets to explore possible mechanisms that account for the pathogenesis of SARS-CoV and AD. The work is further extended to unveil the molecular interactions of APOE4 and NLRP3 with the ACE2-Spike protein complex at the molecular level by employing molecular dynamics simulation techniques. The therapeutic efficacy of Chyawanprash nutraceuticals is evaluated as their inhibitory potential towards APOE4-ACE2-Spike protein and NLRP3-ACE2-Spike protein complexes. Notably, our simulations unequivocally demonstrate the robust and enduring binding capability of the compound Phyllantidine with the target complexes throughout the simulation period. The findings of the studies further corroborate the primary hypothesis of APOE4 and NLRP3 as driver factors in the pathogenesis of both SARS-CoV and AD. Therefore, this research establishes a paradigm for comprehending the complex interaction between AD and SARS-CoV and lays the groundwork for further study in this domain.Communicated by Ramaswamy H. Sarma.

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来源期刊
Journal of Biomolecular Structure & Dynamics
Journal of Biomolecular Structure & Dynamics 生物-生化与分子生物学
CiteScore
8.90
自引率
9.10%
发文量
597
审稿时长
2 months
期刊介绍: The Journal of Biomolecular Structure and Dynamics welcomes manuscripts on biological structure, dynamics, interactions and expression. The Journal is one of the leading publications in high end computational science, atomic structural biology, bioinformatics, virtual drug design, genomics and biological networks.
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