对 SARS-CoV-2 和根瘤蚜的 IMPDH 酶和 RNA 依赖性 RNA 聚合酶进行三重硅学靶向。

IF 2.4 4区 生物学 Q3 MICROBIOLOGY Future microbiology Pub Date : 2024-01-01 Epub Date: 2024-01-31 DOI:10.2217/fmb-2023-0103
Abdel-Moniem S Hassan, Abdo A Elfiky, Alaa M Elgohary
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引用次数: 0

摘要

目的:去年,粘孢子菌病与 SARS-CoV-2 感染有关。本研究的目的是对病毒和真菌 RNA 依赖性 RNA 聚合酶(RdRps)和人单磷酸肌苷脱氢酶(IMPDH)进行三重检测。材料与方法:利用分子对接和分子动力学模拟测试了针对 SARS-CoV-2 的 RdRps 和根瘤菌 RdRp 的核苷酸抑制剂(NIs)。这些抑制剂的目标也是 IMPDH。结果四种 NIs 与雷米替韦和索非布韦这两种药物的结合亲和力相当。在 100-ns 分子动力学模拟后,利用 RdRps 最丰富的构象计算出了结合能。结论我们提出了四种 NIs 对致病性 RdRps 和 IMPDH 的三重抑制潜力,值得进行实验验证。
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Triple in silico targeting of IMPDH enzyme and RNA-dependent RNA polymerase of both SARS-CoV-2 and Rhizopus oryzae.

Aim: Mucormycosis has been associated with SARS-CoV-2 infections during the last year. The aim of this study was to triple-hit viral and fungal RNA-dependent RNA polymerases (RdRps) and human inosine monophosphate dehydrogenase (IMPDH). Materials & methods: Molecular docking and molecular dynamics simulation were used to test nucleotide inhibitors (NIs) against the RdRps of SARS-CoV-2 and Rhizopus oryzae RdRp. These same inhibitors targeted IMPDH. Results: Four NIs revealed a comparable binding affinity to the two drugs, remdesivir and sofosbuvir. Binding energies were calculated using the most abundant conformations of the RdRps after 100-ns molecular dynamics simulation. Conclusion: We suggest the triple-inhibition potential of four NIs against pathogenic RdRps and IMPDH, which is worth experimental validation.

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来源期刊
Future microbiology
Future microbiology 生物-微生物学
CiteScore
4.90
自引率
3.20%
发文量
134
审稿时长
6-12 weeks
期刊介绍: Future Microbiology delivers essential information in concise, at-a-glance article formats. Key advances in the field are reported and analyzed by international experts, providing an authoritative but accessible forum for this increasingly important and vast area of research.
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