Khalili Saeed, Jahangiri Abolfazl, Hashemi Zahra Sadat, Khalesi Bahman, Mard-Soltani Maysam, Amani Jafar
Applied Microbiology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Department of Medical Biotechnology, School of Advanced Medical Technologies, Tehran University of Medical Science, Tehran, Iran.
Toxicon. 2017 Mar 1;127:90-99. doi: 10.1016/j.toxicon.2017.01.010. Epub 2017 Jan 12.
Epsilon toxin of the Clostridium perfringens garnered a lot of attention due to its potential for toxicity in humans, extreme potency for cytotoxicity in mice and lack of any approved therapeutics prescribed for human. However, the intricacies of the Epsilon toxin action mechanism are yet to be understood. In this regard, various in silico tools have been exploited to model and refine the 3D structure of the toxin and its two receptors. The receptor proteins were embedded into designed lipid membranes within an aqueous and ionized environment. Thereafter, the modeled structures subjected to series of consecutive molecular dynamics runs to achieve the most natural like coordination for each model. Ultimately, protein-protein interaction analyses were performed to understand the probable action mechanism. The obtained results successfully confirmed the accuracy of employed methods to achieve high quality models for the toxin and its receptors within their lipid bilayers. Molecular dynamics analyses lead the structures to a more native like coordination. Moreover, the results of previous empirical studies were confirmed, while new insights for action mechanisms including the detailed roles of Hepatitis A virus cellular receptor 1 (HAVCR1) and Myelin and lymphocyte protein (MAL) proteins were achieved. In light of previous and our observations, we suggested novel models which elucidated the existing interplay between potential players of Epsilon toxin action mechanism with detailed structural evidences. These models would pave the way to have more robust understanding of the Epsilon toxin biology, more precise vaccine construction and more successful drug (inhibitor) design.
产气荚膜梭菌的ε毒素因其对人类的潜在毒性、对小鼠细胞毒性的极高效力以及缺乏任何获批用于人类的治疗方法而备受关注。然而,ε毒素作用机制的复杂性仍有待了解。在这方面,已利用各种计算机工具对毒素及其两种受体的三维结构进行建模和优化。受体蛋白被嵌入水相和离子化环境中的设计脂质膜内。此后,对建模结构进行一系列连续的分子动力学运行,以实现每个模型最接近天然的配位。最终,进行蛋白质-蛋白质相互作用分析以了解可能的作用机制。获得的结果成功证实了所采用方法的准确性,能够在脂质双层中为毒素及其受体实现高质量模型。分子动力学分析使结构达到更接近天然的配位。此外,先前实证研究的结果得到了证实,同时获得了关于作用机制的新见解,包括甲型肝炎病毒细胞受体1(HAVCR1)和髓磷脂与淋巴细胞蛋白(MAL)蛋白的详细作用。根据先前的观察和我们的观察结果,我们提出了新的模型,这些模型通过详细的结构证据阐明了ε毒素作用机制潜在参与者之间现有的相互作用。这些模型将为更深入地理解ε毒素生物学、更精确的疫苗构建和更成功的药物(抑制剂)设计铺平道路。