抗SARS-CoV-2病毒RNA依赖性RNA聚合酶复合物(nsp7/nsp8/nsp12)的植物源性天然非核苷类似物抑制剂(NNAIs)

IF 1.9 Q3 NUTRITION & DIETETICS Journal of Dietary Supplements Pub Date : 2023-01-01 DOI:10.1080/19390211.2021.2006387
Sreus A G Naidu, Ghulam Mustafa, Roger A Clemens, A Satyanarayan Naidu
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引用次数: 10

摘要

快速传播的SARS-CoV-2突变体的出现引发了COVID-19大流行的新阶段。目前迫切需要针对SARS-CoV-2上不易突变的高度保守的基因组结构域开发抗病毒药物。nsp12,也被称为rna依赖性rna聚合酶(RdRp),是“SARS-CoV-2复制转录复合体”的核心成分,是一个潜在的保守的可药物抗病毒靶点。fda批准的几种RdRp“核苷酸类似物抑制剂”(NAIs),如remdesivir,已被重新用于治疗COVID-19感染。nai靶向RdRp蛋白的翻译,并竞争性地阻断核苷酸插入RNA链,从而抑制病毒复制。然而,nsp14-ExoN的复制校对功能可以提供对SARS-CoV-2对许多nai的抗性。相反,“非核苷类似物抑制剂(NNAIs)”与病毒聚合酶表面的变构位点结合,改变氧化还原状态;因此,通过改变酶底物与RdRp活性核心催化位点之间的相互作用来发挥抗病毒活性。NNAIs不需要代谢激活(与NAIs不同),也不与细胞内三磷酸核苷酸(NTPs)竞争抗rdrp活性。与合成的nnai相比,来自植物营养素的nnai是潜在的抗病毒候选物。一些计算机上的研究报道了天然植物营养素- nnai的抗病毒谱,如苏拉明、水飞蓟宾(黄酮木质素)、茶黄素(茶多酚)、黄芩素(5,6,7-三羟基黄酮)、花椰菜素(没食子单宁)、橙皮苷(柑橘类生物类黄酮)、石蒜碱(吡啶生物碱),它们比抗病毒药物(如瑞德西韦、法维拉韦)具有更好的氧化还原特性(自由结合能、氢键等)。这些植物营养素- nnai还具有抗炎、抗氧化、免疫调节和心脏保护功能,在COVID-19的临床管理中具有多功能治疗益处。
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Plant-Derived Natural Non-Nucleoside Analog Inhibitors (NNAIs) against RNA-Dependent RNA Polymerase Complex (nsp7/nsp8/nsp12) of SARS-CoV-2.

The emergence of fast-spreading SARS-CoV-2 mutants has sparked a new phase of COVID-19 pandemic. There is a dire necessity for antivirals targeting highly conserved genomic domains on SARS-CoV-2 that are less prone to mutation. The nsp12, also known as the RNA-dependent RNA-polymerase (RdRp), the core component of 'SARS-CoV-2 replication-transcription complex', is a potential well-conserved druggable antiviral target. Several FDA-approved RdRp 'nucleotide analog inhibitors (NAIs)' such as remdesivir, have been repurposed to treat COVID-19 infections. The NAIs target RdRp protein translation and competitively block the nucleotide insertion into the RNA chain, resulting in the inhibition of viral replication. However, the replication proofreading function of nsp14-ExoN could provide resistance to SARS-CoV-2 against many NAIs. Conversely, the 'non-nucleoside analog inhibitors (NNAIs)' bind to allosteric sites on viral polymerase surface, change the redox state; thereby, exert antiviral activity by altering interactions between the enzyme substrate and active core catalytic site of the RdRp. NNAIs neither require metabolic activation (unlike NAIs) nor compete with intracellular pool of nucleotide triphosphates (NTPs) for anti-RdRp activity. The NNAIs from phytonutrient origin are potential antiviral candidates compared to their synthetic counterparts. Several in-silico studies reported the antiviral spectrum of natural phytonutrient-NNAIs such as Suramin, Silibinin (flavonolignan), Theaflavin (tea polyphenol), Baicalein (5,6,7-trihydroxyflavone), Corilagin (gallotannin), Hesperidin (citrus bioflavonoid), Lycorine (pyrrolidine alkaloid), with superior redox characteristics (free binding energy, hydrogen-bonds, etc.) than antiviral drugs (i.e. remdesivir, favipiravir). These phytonutrient-NNAIs also exert anti-inflammatory, antioxidant, immunomodulatory and cardioprotective functions, with multifunctional therapeutic benefits in the clinical management of COVID-19.

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来源期刊
Journal of Dietary Supplements
Journal of Dietary Supplements Agricultural and Biological Sciences-Food Science
CiteScore
6.10
自引率
0.00%
发文量
34
期刊介绍: The Journal of Dietary Supplements (formerly the Journal of Nutraceuticals, Functional & Medical Foods) has been retitled to reflect the bold departure from a traditional scientific journal presentation to a leading voice for anyone with a stake in dietary supplements. The journal addresses important issues that meet the broad range of interests from researchers, regulators, marketers, educators, and health professionals from academic, governmental, industry, healthcare, public health, and consumer education sectors. This vital tool not only presents scientific information but interprets it - helping you more readily pass it on to your students, patients, clients, or company.
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