用分子动力学模拟比较分析三柱和四柱合成葡萄糖受体:一个案例研究。

IF 2.4 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rajesh Kondabala, Vijay Kumar, Amjad Ali
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引用次数: 0

摘要

计算分子模型的进步极大地促进了合成葡萄糖受体的发展,解决了葡萄糖识别中最具挑战性的问题之一。本研究探讨了三柱和四柱合成葡萄糖受体的设计和分析。利用极性(1,2-二(3-甲基脲)苯)柱结合苯、联苯和菲片段作为极性表面,我们设计了新的受体。我们的分子动力学模拟表明,苯是最有利的极性片段创造合成葡萄糖受体。进一步的模拟将三聚三甲、三甲基三聚三甲、三乙基三聚三甲和三甲酰基三聚三甲作为极性片段与(1,2-二(3-甲基脲)苯)极性柱结合,表明具有三乙基三聚三甲和三甲酰基三聚三甲的受体具有稳定的构象。合成葡萄糖受体代表了葡萄糖相关疾病和疾病治疗的未来。这些受体具有广泛的应用,包括作为葡萄糖载体和葡萄糖提取物。使用3D Builder工具构建受体的三维结构,然后通过MacroModel应用程序进行能量最小化。葡萄糖-受体相互作用姿势使用GLIED工具预测。使用Berendsen恒温器和气压调节器进行计算。采用基于gpu的DESMOND软件,采用OPLS2005力场和TIP3P溶剂模型,采用Langevin系综方法进行了分子动力学(MD)模拟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative analysis of three-pillared and four-pillared synthetic glucose receptor using molecular dynamics simulations: a case study.

The advancement of computational molecular modeling has significantly enhanced the development of synthetic glucose receptors, addressing one of the most challenging problems in glucose recognition. This study explores the design and analysis of both three-pillared and four-pillared synthetic glucose receptors. Using polar (1,2-Bis(3-methylureido)benzene) pillars combined with benzene, biphenyl, and phenanthrene fragments as apolar surfaces, we have designed novel receptors. Our molecular dynamics simulations reveal that benzene is the most favorable apolar fragment for creating synthetic glucose receptors. Further simulations incorporating Mesitylene, Trimethylmesitylene, Triethylmesitylene, and Triptopylmesitylene as apolar fragments with (1,2-Bis(3-methylureido)benzene) polar pillars demonstrate that receptors with Triethylmesitylene and Triptopylmesitylene exhibit stable conformations. Synthetic glucose receptors represent the future of therapeutics for glucose-related disorders and conditions. These receptors have wide-ranging applications, including functioning as glucose carriers and glucose extractors. The 3D structures of the receptors were constructed using the 3D Builder tool, followed by energy minimization via the MacroModel application. The glucose-receptor interaction poses were predicted using the GLIED tool. Calculations were performed using the Berendsen thermostat and barostat. Molecular dynamics (MD) simulations were conducted with the Langevin ensemble method, utilizing GPU-based DESMOND software with the OPLS2005 force field and the TIP3P solvent model.

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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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