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分析显示,zonulin抑制剂醋酸兰瑞肽具有潜在的抗SARS-CoV-2主要蛋白酶活性。

Analysis Revealed Potential Anti-SARS-CoV-2 Main Protease Activity by the Zonulin Inhibitor Larazotide Acetate.

作者信息

Di Micco Simone, Musella Simona, Scala Maria C, Sala Marina, Campiglia Pietro, Bifulco Giuseppe, Fasano Alessio

机构信息

European Biomedical Research Institute of Salerno (EBRIS), Salerno, Italy.

Department of Pharmacy, University of Salerno, Salerno, Italy.

出版信息

Front Chem. 2021 Jan 15;8:628609. doi: 10.3389/fchem.2020.628609. eCollection 2020.

Abstract

The most severe outcome of COVID-19 infection is the development of interstitial pneumonia causing acute lung injury (ALI) and/or acute respiratory distress syndrome (ARDS), both responsible for the infected patients' mortality. ALI and ARDS are characterized by a leakage of plasma components into the lungs, compromising their ability to expand and optimally engage in gas exchange with blood, resulting in respiratory failure. We have previously reported that zonulin, a protein dictating epithelial and endothelial permeability in several districts, including the airways, is involved in ALI pathogenesis in mouse models, and that its peptide inhibitor Larazotide acetate (also called AT1001) ameliorated ALI and subsequent mortality by decreasing mucosal permeability to fluid and extravasation of neutrophils into the lungs. With the recent crystallographic resolution of the SARS-CoV-2 main protease (M), an enzyme fundamental in the viral lifecycle, bound to peptidomimetic inhibitors N3 and 13b, we were able to perform molecular modeling investigation showing that AT1001 presents structural motifs similar to co-crystallized ligands. Specifically, molecular docking, MM-GBSA-based predictions and molecular dynamics showed that AT1001 docks extremely well in the M catalytic domain through a global turn conformational arrangement without any unfavorable steric hindrance. Finally, we have observed that AT1001 can be superimposed onto the crystallized structures of N3 and 13b, establishing a higher number of interactions and accordingly a tighter binding. studies confirmed AT1001 anti-M and preliminary investigation indicted an anti-viral activity. Combined, these studies suggest that AT1001, besides its well-demonstrated effect in ameliorating mucosal permeability in ALI/ARDS, may also exert a direct anti-SARS-CoV-2 effect by blocking the M. AT1001 has been used extensively in a variety of animal models of ALI demonstrating robust safety and efficacy; it is currently in phase 3 trials in celiac subjects showing strong safety and efficacy profiles. We therefore propose its use as a specific anti-SARS-CoV-2 multitargeting treatment for the current pandemic.

摘要

新型冠状病毒肺炎(COVID-19)感染最严重的后果是发展为间质性肺炎,导致急性肺损伤(ALI)和/或急性呼吸窘迫综合征(ARDS),这两者都是感染患者死亡的原因。ALI和ARDS的特征是血浆成分渗漏到肺部,损害了肺部扩张以及与血液进行最佳气体交换的能力,从而导致呼吸衰竭。我们之前报道过,zonulin这种在包括气道在内的多个区域决定上皮和内皮通透性的蛋白质,参与了小鼠模型中ALI的发病机制,并且其肽抑制剂醋酸拉佐替德(也称为AT1001)通过降低黏膜对液体的通透性以及中性粒细胞向肺部的渗出,改善了ALI及随后的死亡率。随着最近对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)主要蛋白酶(M)(一种在病毒生命周期中起关键作用的酶)与拟肽抑制剂N3和13b结合的晶体结构解析,我们能够进行分子模拟研究,结果表明AT1001呈现出与共结晶配体相似的结构基序。具体而言,分子对接、基于MM-GBSA的预测以及分子动力学表明,AT1001通过一种全局扭转构象排列在M催化结构域中对接得非常好,没有任何不利的空间位阻。最后,我们观察到AT1001可以叠加到N3和13b的晶体结构上,建立更多的相互作用,从而实现更紧密的结合。研究证实了AT1001对M的作用,初步研究表明其具有抗病毒活性。综合来看,这些研究表明,AT1001除了在改善ALI/ARDS中的黏膜通透性方面有充分证明的效果外,还可能通过阻断M发挥直接的抗SARS-CoV-2作用。AT1001已在多种ALI动物模型中广泛使用,显示出强大的安全性和有效性;它目前正在乳糜泻患者中进行3期试验,显示出良好的安全性和有效性。因此,我们建议将其用作针对当前大流行的特异性抗SARS-CoV-2多靶点治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/414c/7843458/786fa027bf8c/fchem-08-628609-g0001.jpg

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