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通过分子对接和分子动力学模拟靶向抑制ACE2来研究基于潜在免疫营养的运动补充剂对抗COVID-19的作用。

study of potential immunonutrient-based sports supplements against COVID-19 via targeting ACE2 inhibition using molecular docking and molecular dynamics simulations.

作者信息

Banitalebi Ebrahim, Abdizadeh Tooba, Khademi Dehkordi Maryam, Saghaei Elham, Mardaniyan Ghahfarrokhi Majid

机构信息

Department of Sport Sciences, Shahrekord University, Shahrekord, Iran.

Clinical Biochemistry Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

出版信息

J Biomol Struct Dyn. 2023 Feb;41(3):1041-1061. doi: 10.1080/07391102.2021.2016489. Epub 2021 Dec 21.

Abstract

Use of some sports supplements can inhibit angiotensin-converting enzyme II (ACE2), a receptor for the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), as reviewed through molecular docking and sequent molecular dynamics (MD) simulations against this condition. The crystal structures of ACE2 receptors of SARS-CoV-2 and SARS-CoV, applied in docking analysis, were taken from the Protein Data Bank (PDB). The receptors were then prepared using the Molecular Operating Environment (MOE), as a drug-discovery software platform for docking. Supplements such as quercetin and beta glucan (β-glucan) were the top docked compounds to ACE2 receptor though they strongly interacted with CoV target protein. The study data showed that immune responses to immunonutrient-based sports compounds (viz. quercetin and β-glucan) in Coronavirus disease 2019 (COVID-19) were essential in mounting successful immune responses by athletes. While awaiting the development of an effective vaccine, there is a need to focus on immunonutrient-based sports supplements as preventive and therapeutic options that can be implemented in a safe and quick manner to bolster immune responses in athletes.Communicated by Ramaswamy H. Sarma.

摘要

通过针对这种情况的分子对接和后续分子动力学(MD)模拟研究发现,某些运动补剂的使用可能会抑制血管紧张素转换酶II(ACE2),而ACE2是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的一种受体。对接分析中使用的SARS-CoV-2和SARS-CoV的ACE2受体晶体结构取自蛋白质数据库(PDB)。然后使用分子操作环境(MOE)对受体进行制备,MOE是一种用于对接的药物发现软件平台。槲皮素和β-葡聚糖等补剂是与ACE2受体对接得分最高的化合物,尽管它们与冠状病毒靶蛋白有强烈相互作用。研究数据表明,2019冠状病毒病(COVID-19)中基于免疫营养的运动化合物(即槲皮素和β-葡聚糖)引发的免疫反应对于运动员成功产生免疫反应至关重要。在等待有效疫苗研发的过程中,有必要将重点放在基于免疫营养的运动补剂上,将其作为可以安全、快速实施的预防和治疗选择,以增强运动员的免疫反应。由拉马斯瓦米·H·萨尔马传达。

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