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治疗性液体混合物及其与分枝杆菌结合的分子动力学研究

Molecular Dynamics Studies of Therapeutic Liquid Mixtures and Their Binding to Mycobacteria.

作者信息

Monteiro Hugo, Santos Filipa, Paiva Alexandre, Duarte Ana Rita C, Ferreira Ricardo J

机构信息

LAQV, REQUIMTE, Chemistry Department of NOVA School of Science and Technology, Caparica, Portugal.

Red Glead Discovery AB, Lund, Sweden.

出版信息

Front Pharmacol. 2021 Apr 20;12:626735. doi: 10.3389/fphar.2021.626735. eCollection 2021.

Abstract

Tuberculosis is an highly contagious disease still considered by the WHO as one of most infectious diseases worldwide. The therapeutic approach, used to prevent and treat tuberculosis targets the complex, comprises a combination of drugs administrated for long periods of time, which, in many cases, could cause several adverse effects and, consequently, low compliance of the patient to the treatment and drug-resistance. Therefore, therapeutic liquid mixtures formulated with anti-tuberculosis drugs and/or adjuvants in tuberculosis therapy are an interesting approach to prevent toxic effects and resistance to anti-tuberculosis drugs. The herein formulated therapeutic liquid mixtures, including ethambutol, arginine, citric acid and water under different molar ratios, were studied through a molecular dynamics approach to understand how ethambutol and arginine could be stabilized by the presence of citric acid and/or water in the mixture. To gain insights on how the uptake of these mixtures into the mycobacteria cell may occur and how a mycobacterial ABC transporter could contribute to this transport, multiple simultaneous ligand docking was performed. Interactions between citric acid and ethambutol involving the carboxyl and hydroxyl groups of citric acid with the amines of ethambutol were identified as the most critical ones. Water molecules present in the mixture provides the necessary network of hydrogen bonds that stabilize the mixture. Molecular docking additionally provided an interesting hypothesis on how the different mixture components may favor binding of ethambutol to an ABC importer. The data presented in this work helps to better understand these mixtures as well as to provide cues on the mechanisms that allow them to cross the mycobacterial cell membrane.

摘要

结核病是一种高度传染性疾病,世界卫生组织仍将其视为全球最具传染性的疾病之一。用于预防和治疗结核病的治疗方法针对该复合体,包括长时间联合使用多种药物,在许多情况下,这可能会导致多种不良反应,进而导致患者对治疗的依从性低和产生耐药性。因此,在结核病治疗中用抗结核药物和/或佐剂配制治疗性液体混合物是一种预防抗结核药物毒性作用和耐药性的有趣方法。本文配制的治疗性液体混合物,包括不同摩尔比的乙胺丁醇、精氨酸、柠檬酸和水,通过分子动力学方法进行了研究,以了解柠檬酸和/或水的存在如何使乙胺丁醇和精氨酸稳定。为了深入了解这些混合物如何进入分枝杆菌细胞以及分枝杆菌ABC转运蛋白如何促进这种转运,进行了多重同时配体对接。柠檬酸与乙胺丁醇之间涉及柠檬酸羧基和羟基与乙胺丁醇胺基的相互作用被确定为最关键的相互作用。混合物中存在的水分子提供了稳定混合物所需的氢键网络。分子对接还提供了一个有趣的假设,即不同的混合物成分如何促进乙胺丁醇与ABC进口蛋白的结合。这项工作中呈现的数据有助于更好地理解这些混合物,并为它们穿越分枝杆菌细胞膜的机制提供线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b98/8096353/76b4a93960f4/fphar-12-626735-g001.jpg

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