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熊去氧胆酸和鹅去氧胆酸的虚拟再利用作为针对 SARS-CoV2-包膜蛋白的先导候选药物:分子动力学研究。

Virtual repurposing of ursodeoxycholate and chenodeoxycholate as lead candidates against SARS-Cov2-Envelope protein: A molecular dynamics investigation.

机构信息

Department of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Department of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

J Biomol Struct Dyn. 2022 Jul;40(11):5147-5158. doi: 10.1080/07391102.2020.1868339. Epub 2020 Dec 31.

Abstract

Drug repurposing is an apt choice to combat the currently prevailing global threat of COVID-19, caused by SARS-Cov2in absence of any specific medication/vaccine. The present work employs state of art computational methods like homology modelling, molecular docking and molecular dynamics simulations to evaluate the potential of two widely used surfactant drugs namely chenodeoxycholate(CDC) and ursodeoxycholate (UDC), to bind to the envelope protein of SARS-Cov2(SARS-Cov2-E).The monomeric unit of SARS-Cov2-E was modelled from a close homologue (>90% sequence identity) and a pentameric assembly was modelled using symmetric docking, followed by energy minimization in a DPPC membrane environment. The minimized structure was used to generate best scoring SARS-Cov2-E-CDC/UDC complexes through blind docking. These complexes were subjected to 230 ns molecular dynamics simulations in triplicates in a DPPC membrane environment. Comparative analyses of structural properties and molecular interaction profiles from the MD trajectories revealed that, both CDC and UDC could stably bind to SARS-Cov2-E through H-bonds, water-bridges and hydrophobic contacts with the transmembrane-channelresidues.T30 was observed to be a key residue for CDC/UDC binding. CDC/UDC binding affected the H-bonding pattern between adjacent monomeric chains, slackening the compact transmembrane region of SARS-Cov2-E. Additionally, the polar functional groups of CDC/UDC facilitated entry of a large number of water molecules into the channel. These observations suggest CDC/UDC as potential candidates to hinder the survival of SARS-Cov2 by disrupting the structure of SARS-Cov2-E and facilitating the entry of solvents/polar inhibitors inside the viral cell.Communicated by Ramaswamy H. Sarma.

摘要

药物重用以对抗当前全球由 SARS-CoV-2 引起的 COVID-19 大流行是一个恰当的选择,因为目前还没有针对这种病毒的特效药物或疫苗。本研究采用同源建模、分子对接和分子动力学模拟等最先进的计算方法,评估两种广泛使用的表面活性剂药物——鹅去氧胆酸(CDC)和熊去氧胆酸(UDC)与 SARS-CoV-2 包膜蛋白(SARS-CoV-2-E)结合的潜力。SARS-CoV-2-E 的单体单元是根据一个密切同源物(>90%序列同一性)建模的,使用对称对接构建五聚体组装体,然后在 DPPC 膜环境中进行能量最小化。使用最小化结构通过盲目对接生成得分最高的 SARS-CoV-2-E-CDC/UDC 复合物。这些复合物在 DPPC 膜环境中进行了 230ns 的分子动力学模拟重复 3 次。通过 MD 轨迹的结构特性和分子相互作用分析比较,发现 CDC 和 UDC 都可以通过氢键、水桥和疏水相互作用与跨膜通道残基稳定结合 SARS-CoV-2-E。T30 被观察到是 CDC/UDC 结合的关键残基。CDC/UDC 结合影响相邻单体链之间氢键的形成模式,使 SARS-CoV-2-E 的紧凑跨膜区域松弛。此外,CDC/UDC 的极性官能团促进了大量水分子进入通道。这些观察结果表明,CDC/UDC 可能通过破坏 SARS-CoV-2-E 的结构并促进溶剂/极性抑制剂进入病毒细胞,成为阻碍 SARS-CoV-2 存活的潜在候选药物。由 Ramaswamy H. Sarma 传达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ab7/7784831/c710069ff8af/TBSD_A_1868339_UF0001_C.jpg

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