Targeting Monkeypox Virus Methyltransferase: Virtual Screening of Natural Compounds from Middle-Eastern Medicinal Plants.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Biotechnology Pub Date : 2024-08-03 DOI:10.1007/s12033-024-01246-y
Hayder O Hashim, Jafar M B Al-Shuhaib, Mudher K Mohammed, Mohammed Baqur S Al-Shuhaib
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Abstract

Monkeypox is an infectious disease resulting from the monkeypox virus, and its fatality rate varies depending on the virus clade and the location of the outbreak. In monkeypox virus, methyltransferase (MTase) plays a crucial role in modifying the cap structure of viral mRNA. This alteration assists the virus in evading the host's immune system, enhances viral protein synthesis, and ultimately enables successful infection and replication within host cells. Given the significance of MTase in viral infection and spread within the host, our study aimed to identify a natural inhibitor for this enzyme using docking and molecular dynamic (MD) simulations. We collected a total of 12,971 natural compounds from 200 medicinal plants in the Middle East. After eliminating duplicate compounds, we had 5,749 unique ligand conformers, which we then subjected to high-throughput virtual screening against MTase. The most promising hits were further evaluated using the extra-precision (XP) tool. The affinity of these hits was also assessed by Prime-Molecular Mechanics/Generalized Born Surface Area (MMGBSA) tool. The analysis revealed that two standard controls (sinefungin and TO1119) and two Middle-Eastern compounds (folic acid and 1,2,4,6-tetragalloylglucose) exhibited the best XP docking scores. According to Prime MMGBSA calculations, the Middle-Eastern compounds showed higher affinities, with values of - 60.61 kcal/mol for 1,2,4,6-tetragalloylglucose and - 51.87 kcal/mol for folic acid, surpassing the controls (TO1119 at - 35.71 kcal/mol and sinefungin at - 31.51 kcal/mol). In the majority of Molecular dynamic (MD) simulations, folic acid exhibited demonstrated greater stability than sinefungin. Further investigation revealed that folic acid occupied a critical position in the active site of MTase, which reduced its interaction with the mRNA substrate. Based on these findings, it can be concluded that folic acid is a highly promising natural compound for potential use in the cost-effective treatment of monkeypox virus. The identification of folic acid as a potential antiviral agent highlights the importance of nature in providing new therapeutic uses that have significant implications for global health, particularly in regions where monkeypox viral outbreaks are prevalent. However, it is essential to note that further wet-lab validations are necessary to confirm its efficacy for treatment in a medical context.

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以猴头痘病毒甲基转移酶为靶标:中东药用植物天然化合物的虚拟筛选。
猴痘是由猴痘病毒引起的一种传染病,其致死率因病毒支系和爆发地点而异。在猴痘病毒中,甲基转移酶(MTase)在改变病毒 mRNA 的帽结构方面起着至关重要的作用。这种改变有助于病毒躲避宿主的免疫系统,增强病毒蛋白质的合成,并最终使病毒在宿主细胞内成功感染和复制。鉴于 MT 酶在病毒感染和宿主体内传播中的重要作用,我们的研究旨在利用对接和分子动力学(MD)模拟找出这种酶的天然抑制剂。我们从中东地区的 200 种药用植物中收集了 12971 种天然化合物。剔除重复化合物后,我们得到了 5,749 个独特的配体构象,然后对这些配体进行了针对 MTase 的高通量虚拟筛选。我们使用超精密(XP)工具进一步评估了最有希望的配体。我们还利用分子机理/广义博恩表面积(Prime-Molecular Mechanics/Generalized Born Surface Area,MMGBSA)工具评估了这些配体的亲和力。分析结果显示,两个标准对照组(正银霉素和 TO1119)和两个中东化合物(叶酸和 1,2,4,6-四ragalloyl-glucose)的 XP 对接得分最高。根据 Prime MMGBSA 计算,中东化合物表现出更高的亲和力,1,2,4,6-四ragalloylglucose 和叶酸的亲和力分别为-60.61 kcal/mol 和-51.87 kcal/mol,超过了对照组(TO1119 为-35.71 kcal/mol,正银杏苷为-31.51 kcal/mol)。在大多数分子动力学(MD)模拟中,叶酸都比正银杏苷表现出更高的稳定性。进一步研究发现,叶酸占据了 MT 酶活性位点的一个关键位置,从而降低了它与 mRNA 底物的相互作用。基于这些发现,可以得出结论,叶酸是一种极有潜力的天然化合物,有望用于猴痘病毒的经济有效治疗。叶酸被鉴定为一种潜在的抗病毒剂,这凸显了大自然在提供新的治疗用途方面的重要性,对全球健康具有重要意义,尤其是在猴痘病毒流行的地区。不过,必须指出的是,要确认叶酸在医疗方面的疗效,还需要进一步的湿实验室验证。
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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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