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基于氧化锌纳米结构油载体的计算机模拟研究,以及 和 的种子提取物作为 SARS-CoV-2 3CL 蛋白酶潜在抑制剂。

In Silico Studies on Zinc Oxide Based Nanostructured Oil Carriers with Seed Extracts of and as Potential Inhibitors of 3CL Protease of SARS-CoV-2.

机构信息

Department of Physics, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh 11671, Saudi Arabia.

Department of Zoology, College of Sciences, King Saud University, Riyadh 11451, Saudi Arabia.

出版信息

Molecules. 2022 Jul 4;27(13):4301. doi: 10.3390/molecules27134301.

Abstract

Coming into the second year of the pandemic, the acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its variants continue to be a serious health hazard globally. A surge in the omicron wave, despite the discovery of the vaccines, has shifted the attention of research towards the discovery and use of bioactive compounds, being potential inhibitors of the viral structural proteins. The present study aimed at the green synthesis of zinc oxide (ZnO) nanoparticles with seed extracts of and -loaded nanostructured oil carriers (NLC)-using a mixture of olive and black seed essential oils. The synthesized ZnO NLC were extensively characterized. In addition, the constituent compounds in ZnO NLC were investigated as a potential inhibitor for the SARS-CoV-2 main protease (3CLpro or Mpro) where 27 bioactive constituents, along with ZnO in the nanostructure, were subjected to molecular docking studies. The resultant high-score compounds were further validated by molecular dynamics simulation. The study optimized the compounds dithymoquinone, δ-hederin, oleuropein, and zinc oxide with high docking energy scores (ranging from -7.9 to -9.9 kcal/mol). The RMSD and RMSF data that ensued also mirrored these results for the stability of proteins and ligands. RMSD and RMSF data showed no conformational change in the protein during the MD simulation. Histograms of every simulation trajectory explained the ligand properties and ligand-protein contacts. Nevertheless, further experimental investigations and validation of the selected candidates are imperative to take forward the applicability of the nanostructure as a potent inhibitor of COVID-19 (Coronavirus Disease 2019) for clinical trials.

摘要

进入大流行的第二年,严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)及其变体继续在全球范围内构成严重的健康威胁。尽管已经发现了疫苗,但由于奥密克戎(omicron)浪潮的出现,研究的重点已经转向发现和使用生物活性化合物,这些化合物可能是病毒结构蛋白的潜在抑制剂。本研究旨在使用橄榄油和黑种草籽油的混合物,通过种子提取物和负载纳米结构油载体(NLC)来绿色合成氧化锌(ZnO)纳米粒子。对合成的 ZnO NLC 进行了广泛的表征。此外,还研究了 ZnO NLC 中的成分化合物作为 SARS-CoV-2 主要蛋白酶(3CLpro 或 Mpro)的潜在抑制剂,其中 27 种生物活性成分以及纳米结构中的 ZnO 都进行了分子对接研究。根据所得高得分化合物进一步进行分子动力学模拟验证。该研究优化了化合物二硫代莫诺苯醌、δ-芹黄素、橄榄苦苷和氧化锌,这些化合物的对接能得分较高(范围为-7.9 至-9.9 kcal/mol)。随之而来的 RMSD 和 RMSF 数据也反映了这些结果,即蛋白质和配体的稳定性。在 MD 模拟过程中,RMSD 和 RMSF 数据显示蛋白质没有构象变化。每个模拟轨迹的柱状图解释了配体的性质和配体-蛋白质的相互作用。然而,为了将纳米结构作为 COVID-19(2019 年冠状病毒病)的潜在抑制剂应用于临床试验,还需要进一步的实验研究和验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d630/9268682/87ede653a577/molecules-27-04301-g001.jpg

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