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SARS-CoV-2 非结构蛋白 9(NSP9)的结构、能量和脂溶性分析。

Structural, energetic and lipophilic analysis of SARS-CoV-2 non-structural protein 9 (NSP9).

机构信息

Laboratório de Planejamento e Desenvolvimento de Fármacos, Instituto de Ciências Exatas e Naturais, Universidade Federal do Pará, Rua Augusto Corrêa 01, 66075-110, Belém, Pará, Brasil.

School of Chemistry & Faculty of Pharmacy, University of Costa Rica, San Pedro, San José, Costa Rica.

出版信息

Sci Rep. 2021 Nov 26;11(1):23003. doi: 10.1038/s41598-021-02366-0.

Abstract

In SARS-CoV-2 replication complex, the Non-structural protein 9 (Nsp9) is an important RNA binding subunit in the RNA-synthesizing machinery. The dimeric forms of coronavirus Nsp9 increase their nucleic acid binding affinity and the N-finger motif appears to play a critical role in dimerization. Here, we present a structural, lipophilic and energetic study about the Nsp9 dimer of SARS-CoV-2 through computational methods that complement hydrophobicity scales of amino acids with molecular dynamics simulations. Additionally, we presented a virtual N-finger mutation to investigate whether this motif contributes to dimer stability. The results reveal for the native dimer that the N-finger contributes favorably through hydrogen bond interactions and two amino acids bellowing to the hydrophobic region, Leu45 and Leu106, are crucial in the formation of the cavity for potential drug binding. On the other hand, Gly100 and Gly104, are responsible for stabilizing the α-helices and making the dimer interface remain stable in both, native and mutant (without N-finger motif) systems. Besides, clustering results for the native dimer showed accessible cavities to drugs. In addition, the energetic and lipophilic analysis reveal that the higher binding energy in the native dimer can be deduced since it is more lipophilic than the mutant one, increasing non-polar interactions, which is in line with the result of MM-GBSA and SIE approaches where the van der Waals energy term has the greatest weight in the stability of the native dimer. Overall, we provide a detailed study on the Nsp9 dimer of SARS-CoV-2 that may aid in the development of new strategies for the treatment and prevention of COVID-19.

摘要

在 SARS-CoV-2 复制复合物中,非结构蛋白 9(Nsp9)是 RNA 合成机制中重要的 RNA 结合亚基。冠状病毒 Nsp9 的二聚体形式增加了其核酸结合亲和力,而 N 指模体似乎在二聚化中起着关键作用。在这里,我们通过计算方法对 SARS-CoV-2 的 Nsp9 二聚体进行了结构、亲脂性和能量研究,这些方法通过分子动力学模拟补充了氨基酸的疏水性尺度。此外,我们还提出了一种虚拟的 N 指突变,以研究该模体是否有助于二聚体稳定性。结果表明,对于天然二聚体,N 指通过氢键相互作用有利地贡献,并且位于疏水区下方的两个氨基酸(Leu45 和 Leu106)对于形成潜在药物结合的空腔至关重要。另一方面,Gly100 和 Gly104 负责稳定α-螺旋,并使二聚体界面在天然和突变(无 N 指模体)系统中保持稳定。此外,天然二聚体的聚类结果显示出可接近药物的空腔。此外,能量和亲脂性分析表明,天然二聚体的结合能更高,可以推断出它比突变体更亲脂,增加了非极性相互作用,这与 MM-GBSA 和 SIE 方法的结果一致,其中范德华能项在天然二聚体的稳定性中具有最大权重。总的来说,我们对 SARS-CoV-2 的 Nsp9 二聚体进行了详细的研究,这可能有助于开发 COVID-19 的治疗和预防新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17f1/8626507/2b1439d33e6d/41598_2021_2366_Fig1_HTML.jpg

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