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木质素衍生的低聚物作为有前景的mTOR抑制剂:动力学模拟的见解

Lignin-Derived Oligomers as Promising mTOR Inhibitors: Insights from Dynamics Simulations.

作者信息

Gabellone Sofia, Carotenuto Giovanni, Arcieri Manuel, Bottoni Paolo, Sbanchi Giulia, Castrignanò Tiziana, Piccinino Davide, Liverani Chiara, Saladino Raffaele

机构信息

IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori"-IRST Srl, 47014 Meldola, Italy.

Department of Ecological and Biological Sciences, Tuscia University, Viale dell'Università s.n.c., 01100 Viterbo, Italy.

出版信息

Int J Mol Sci. 2025 Sep 7;26(17):8728. doi: 10.3390/ijms26178728.

Abstract

The mammalian target of rapamycin pathway, mTOR, is a crucial signaling pathway that regulates cell growth, proliferation, metabolism, and survival. Due to its dysregulation it is involved in several ailments such as cancer or age-related diseases. The discovery of mTOR and the understanding of its biological functions were greatly facilitated by the use of rapamycin, an antibiotic of natural origin, which allosterically inhibits mTORC1, effectively blocking its function. In this entirely computational study, we investigated mTOR's interaction with seven ligands: two clinically established inhibitors (everolimus and rapamycin) and five lignin-derived oligomers, a renewable natural polyphenol recently used for the drug delivery of everolimus. The seven complexes were analyzed through all-atom molecular dynamics simulations in explicit solvent using a high-performance computing platform. Trajectory analyses revealed stable interactions between mTOR and all ligands, with lignin-derived compounds showing comparable or enhanced binding stability relative to reference drugs. To evaluate the stability of the molecular complex and the behavior of the ligand over time, we analyzed key parameters including root mean square deviation, root mean square fluctuation, number of hydrogen bonds, binding free energy, and conformational dynamics assessed through principal component analysis. Our results suggest that lignin fragments are a promising, sustainable scaffold for developing novel mTOR inhibitors.

摘要

雷帕霉素作用的哺乳动物靶点(mTOR)是一条关键的信号通路,可调节细胞生长、增殖、代谢和存活。由于其失调,它与多种疾病有关,如癌症或与年龄相关的疾病。雷帕霉素(一种天然来源的抗生素)的使用极大地促进了mTOR的发现及其生物学功能的理解,雷帕霉素可别构抑制mTORC1,有效阻断其功能。在这项完全基于计算的研究中,我们研究了mTOR与七种配体的相互作用:两种临床应用的抑制剂(依维莫司和雷帕霉素)以及五种木质素衍生的低聚物,木质素是一种可再生的天然多酚,最近被用于依维莫司的药物递送。使用高性能计算平台,通过在显式溶剂中的全原子分子动力学模拟对这七种复合物进行了分析。轨迹分析揭示了mTOR与所有配体之间的稳定相互作用,与参考药物相比,木质素衍生的化合物显示出相当或更高的结合稳定性。为了评估分子复合物的稳定性和配体随时间的行为,我们分析了包括均方根偏差、均方根波动、氢键数量、结合自由能以及通过主成分分析评估的构象动力学等关键参数。我们的结果表明,木质素片段是开发新型mTOR抑制剂的一种有前景的、可持续的支架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d995/12429072/674418a6a3b7/ijms-26-08728-g001.jpg

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