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通过监督分子动力学揭示亚千道尔顿大环肽对凝血酶的分子识别

Shedding Light on the Molecular Recognition of Sub-Kilodalton Macrocyclic Peptides on Thrombin by Supervised Molecular Dynamics.

作者信息

Hassankalhori Mahdi, Bolcato Giovanni, Bissaro Maicol, Sturlese Mattia, Moro Stefano

机构信息

Molecular Modeling Section (MMS), Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.

出版信息

Front Mol Biosci. 2021 Aug 31;8:707661. doi: 10.3389/fmolb.2021.707661. eCollection 2021.

Abstract

Macrocycles are attractive structures for drug development due to their favorable structural features, potential in binding to targets with flat featureless surfaces, and their ability to disrupt protein-protein interactions. Moreover, large novel highly diverse libraries of low-molecular-weight macrocycles with therapeutically favorable characteristics have been recently established. Considering the mentioned facts, having a validated, fast, and accurate computational protocol for studying the molecular recognition and binding mode of this interesting new class of macrocyclic peptides deemed to be helpful as well as insightful in the quest of accelerating drug discovery. To that end, the ability of the in-house supervised molecular dynamics protocol called SuMD in the reproduction of the X-ray crystallography final binding state of a macrocyclic non-canonical tetrapeptide-from a novel library of 8,988 sub-kilodalton macrocyclic peptides-in the thrombin active site was successfully validated. A comparable binding mode with the minimum root-mean-square deviation (RMSD) of 1.4 Å at simulation time point 71.6 ns was achieved. This method validation study extended the application domain of the SuMD sampling method for computationally cheap, fast but accurate, and insightful macrocycle-protein molecular recognition studies.

摘要

大环化合物因其有利的结构特征、与无特征平面表面靶点结合的潜力以及破坏蛋白质-蛋白质相互作用的能力,成为药物开发中具有吸引力的结构。此外,最近已经建立了大量具有治疗有利特性的新型低分子量大环化合物高度多样化文库。考虑到上述事实,拥有一个经过验证的、快速且准确的计算方案来研究这类有趣的新型大环肽的分子识别和结合模式,在加速药物发现的探索中被认为是有帮助且有洞察力的。为此,名为SuMD的内部监督分子动力学方案在重现一种大环非经典四肽(来自一个包含8988个低于千道尔顿的大环肽的新型文库)在凝血酶活性位点的X射线晶体学最终结合状态方面的能力得到了成功验证。在模拟时间点71.6纳秒时实现了具有1.4埃最小均方根偏差(RMSD)的可比结合模式。这项方法验证研究扩展了SuMD采样方法在计算成本低、快速但准确且有洞察力的大环-蛋白质分子识别研究中的应用领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a675/8438215/bc821eff5ee3/fmolb-08-707661-g001.jpg

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