• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

鉴定生物膜拮抗蛋白的潜在抑制剂以促进生物膜形成:虚拟筛选和分子动力学模拟方法。

Identifying potential inhibitors of biofilm-antagonistic proteins to promote biofilm formation: a virtual screening and molecular dynamics simulations approach.

机构信息

WATER Laboratory, Department of Biosciences, Sri Sathya Sai Institute of Higher Learning, Prasanthi Nilayam, Puttaparthi, Andhra Pradesh, 515134, India.

出版信息

Mol Divers. 2022 Aug;26(4):2135-2147. doi: 10.1007/s11030-021-10320-5. Epub 2021 Sep 21.

DOI:10.1007/s11030-021-10320-5
PMID:34546549
Abstract

Microbial biofilms play a critical role in environmental biotechnology and associated applications. Biofilm production can be enhanced by inhibiting the function of proteins that negatively regulate their formation. With this objective, an in silico approach was adopted to identify competitive inhibitors of eight biofilm-antagonistic proteins, namely AbrB and SinR (from Bacillus subtilis) and AmrZ, PDE (EAL), PslG, RetS, ShrA and TpbA (from Pseudomonas aeruginosa). Fifteen inhibitors that structurally resembled the natural ligand of each protein were shortlisted using ligand-based and structure-based virtual screening. The top four inhibitors obtained from molecular docking using Autodock Vina were further docked using SwissDock and DOCK 6.9 to obtain a consensus hit for each protein based on different scoring functions. Further analysis of the protein-ligand complexes revealed that these top inhibitors formed significant non-covalent interactions with their respective protein binding sites. The eight protein-ligand complexes were then subjected to molecular dynamics simulations for 30 ns using GROMACS. RMSD and radius of gyration values of 0.1-0.4 nm and 1.0-3.5 nm, respectively, along with hydrogen bond formation throughout the trajectory indicated that all the complexes remained stable, compact and intact during the simulation period. Binding energy values between -20 and -77 kJ/mol obtained from MM-PBSA calculations further confirmed the high affinities of the eight inhibitors for their respective receptors. The outcome of this study holds great promise to enhance biofilms that are central to biotechnological processes associated with microbial electrochemical technologies, wastewater treatment, bioremediation and the industrial production of value-added products.

摘要

微生物生物膜在环境生物技术及相关应用中起着至关重要的作用。通过抑制负调控其形成的蛋白质的功能,可以增强生物膜的产生。为此,采用了一种计算方法来识别八种生物膜拮抗蛋白(即来自枯草芽孢杆菌的 AbrB 和 SinR 以及来自铜绿假单胞菌的 AmrZ、PDE(EAL)、PslG、RetS、ShrA 和 TpbA)的竞争性抑制剂。使用基于配体和基于结构的虚拟筛选,从短名单中筛选出了 15 种结构上与每种蛋白质天然配体相似的抑制剂。使用 Autodock Vina 进行分子对接获得的前四个抑制剂,进一步使用 SwissDock 和 DOCK 6.9 进行对接,根据不同的评分函数为每种蛋白质获得共识命中。对蛋白质-配体复合物的进一步分析表明,这些顶级抑制剂与各自的蛋白质结合位点形成了重要的非共价相互作用。然后,将这 8 个蛋白质-配体复合物使用 GROMACS 进行 30ns 的分子动力学模拟。0.1-0.4nm 和 1.0-3.5nm 范围内的 RMSD 和旋转半径值以及整个轨迹中氢键的形成表明,在模拟过程中,所有复合物都保持稳定、紧凑和完整。从 MM-PBSA 计算得出的-20 到-77kJ/mol 之间的结合能值进一步证实了这 8 种抑制剂与各自受体的高亲和力。这项研究的结果有望增强与微生物电化学技术、废水处理、生物修复和增值产品工业生产相关的生物技术过程中的生物膜。

相似文献

1
Identifying potential inhibitors of biofilm-antagonistic proteins to promote biofilm formation: a virtual screening and molecular dynamics simulations approach.鉴定生物膜拮抗蛋白的潜在抑制剂以促进生物膜形成:虚拟筛选和分子动力学模拟方法。
Mol Divers. 2022 Aug;26(4):2135-2147. doi: 10.1007/s11030-021-10320-5. Epub 2021 Sep 21.
2
Virtual screening of flavonoids as potential RIPK1 inhibitors for neurodegeneration therapy.作为神经退行性疾病治疗潜在RIPK1抑制剂的黄酮类化合物的虚拟筛选。
PeerJ. 2024 Jan 22;12:e16762. doi: 10.7717/peerj.16762. eCollection 2024.
3
A novel identification approach for discovery of 5-HydroxyTriptamine 2A antagonists: combination of 2D/3D similarity screening, molecular docking and molecular dynamics.一种用于发现 5-羟色胺 2A 拮抗剂的新型鉴定方法:二维/三维相似性筛选、分子对接和分子动力学的组合。
J Biomol Struct Dyn. 2019 Mar;37(4):931-943. doi: 10.1080/07391102.2018.1444509. Epub 2018 Mar 5.
4
Inhibition and disintegration of biofilm with small molecule inhibitors identified through virtual screening for targeting TasA, the major protein component of ECM.通过虚拟筛选鉴定出的针对胞外基质主要蛋白质成分TasA的小分子抑制剂对生物膜的抑制和瓦解作用
J Biomol Struct Dyn. 2023 Apr;41(6):2431-2447. doi: 10.1080/07391102.2022.2033135. Epub 2022 Jan 31.
5
Molecular docking and simulation studies against nucleoside diphosphate kinase (NDK) of with secondary metabolite identified by genome mining from .利用基因组挖掘从 中鉴定的次生代谢产物对核苷二磷酸激酶(NDK)进行分子对接和模拟研究。
J Biomol Struct Dyn. 2023;41(22):12610-12619. doi: 10.1080/07391102.2023.2167118. Epub 2023 Jan 18.
6
Synthesis, Molecular Docking, Molecular Dynamics Studies, and Biological Evaluation of 4H-Chromone-1,2,3,4-tetrahydropyrimidine-5-carboxylate Derivatives as Potential Antileukemic Agents.4H-色酮-1,2,3,4-四氢嘧啶-5-羧酸衍生物的合成、分子对接、分子动力学研究及作为潜在抗白血病药物的生物学评价。
J Chem Inf Model. 2017 Jun 26;57(6):1246-1257. doi: 10.1021/acs.jcim.6b00138. Epub 2017 May 25.
7
Response regulator GacA and transcriptional activator RhlR proteins involved in biofilm formation of Pseudomonas aeruginosa are prospective targets for natural lead molecules: Computational modelling, molecular docking and dynamic simulation studies.参与铜绿假单胞菌生物膜形成的反应调节蛋白 GacA 和转录激活蛋白 RhlR 是天然铅分子的潜在靶点:计算建模、分子对接和动态模拟研究。
Infect Genet Evol. 2020 Nov;85:104448. doi: 10.1016/j.meegid.2020.104448. Epub 2020 Jul 1.
8
Computational screening of natural compounds as putative quorum sensing inhibitors targeting drug resistance bacteria: Molecular docking and molecular dynamics simulations.计算筛选天然化合物作为针对耐药细菌的群体感应抑制剂的研究:分子对接和分子动力学模拟。
Comput Biol Med. 2022 Jun;145:105517. doi: 10.1016/j.compbiomed.2022.105517. Epub 2022 Apr 12.
9
Identification of New Potential Inhibitors of Quorum Sensing through a Specialized Multi-Level Computational Approach.通过一种专门的多层次计算方法鉴定群体感应的新型潜在抑制剂。
Molecules. 2021 Apr 29;26(9):2600. doi: 10.3390/molecules26092600.
10
Carboxylic acid derivatives display potential selectivity for human histone deacetylase 6: Structure-based virtual screening, molecular docking and dynamics simulation studies.羧酸衍生物对人组蛋白去乙酰化酶 6 具有潜在的选择性:基于结构的虚拟筛选、分子对接和动力学模拟研究。
Comput Biol Chem. 2018 Aug;75:131-142. doi: 10.1016/j.compbiolchem.2018.05.004. Epub 2018 May 16.

引用本文的文献

1
Beneficial Biofilms: a Minireview of Strategies To Enhance Biofilm Formation for Biotechnological Applications.有益生物膜:促进生物膜形成的生物技术应用策略简述
Appl Environ Microbiol. 2022 Feb 8;88(3):e0199421. doi: 10.1128/AEM.01994-21. Epub 2021 Dec 1.

本文引用的文献

1
Identification of bioactive compounds from as possible inhibitor of SARS-CoV-2 spike glycoprotein and non-structural protein-15: a pharmacoinformatics study.从 中鉴定出的生物活性化合物可能是 SARS-CoV-2 刺突糖蛋白和非结构蛋白 15 的抑制剂:一项基于计算药理学的研究。
J Biomol Struct Dyn. 2021 Aug;39(13):4686-4700. doi: 10.1080/07391102.2020.1779132. Epub 2020 Jun 18.
2
An investigation into the identification of potential inhibitors of SARS-CoV-2 main protease using molecular docking study.利用分子对接研究鉴定 SARS-CoV-2 主蛋白酶潜在抑制剂的研究。
J Biomol Struct Dyn. 2021 Jun;39(9):3347-3357. doi: 10.1080/07391102.2020.1763201. Epub 2020 May 13.
3
Molecular docking and molecular dynamics simulation approach to screen natural compounds for inhibition of by targeting peptide deformylase.
采用分子对接和分子动力学模拟方法筛选针对肽基脱甲酰酶的天然化合物抑制 。
J Biomol Struct Dyn. 2021 Feb;39(3):823-840. doi: 10.1080/07391102.2020.1719200. Epub 2020 Jan 30.
4
Identification of Zika Virus NS2B-NS3 Protease Inhibitors by Structure-Based Virtual Screening and Drug Repurposing Approaches.基于结构的虚拟筛选和药物再利用方法鉴定 Zika 病毒 NS2B-NS3 蛋白酶抑制剂。
J Chem Inf Model. 2020 Feb 24;60(2):731-737. doi: 10.1021/acs.jcim.9b00933. Epub 2019 Dec 31.
5
Identification of the potential dual inhibitor of protein tyrosine phosphatase sigma and leukocyte common antigen-related phosphatase by virtual screen, molecular dynamic simulations and post-analysis.通过虚拟筛选、分子动力学模拟和后分析鉴定蛋白酪氨酸磷酸酶 sigma 和白细胞共同抗原相关磷酸酶的潜在双重抑制剂。
J Biomol Struct Dyn. 2021 Jan;39(1):45-62. doi: 10.1080/07391102.2019.1705913. Epub 2019 Dec 27.
6
Helix Cracking Regulates the Critical Interaction between RetS and GacS in Pseudomonas aeruginosa.螺旋破解调控铜绿假单胞菌中 RetS 和 GacS 的关键相互作用。
Structure. 2019 May 7;27(5):785-793.e5. doi: 10.1016/j.str.2019.02.006. Epub 2019 Mar 14.
7
Electroactive microorganisms in bioelectrochemical systems.生物电化学系统中的电活性微生物。
Nat Rev Microbiol. 2019 May;17(5):307-319. doi: 10.1038/s41579-019-0173-x.
8
Serine Hydroxymethyltransferase ShrA (PA2444) Controls Rugose Small-Colony Variant Formation in .丝氨酸羟甲基转移酶ShrA(PA2444)控制……中粗糙小菌落变体的形成 。 (原文中“in”后面缺少具体内容)
Front Microbiol. 2018 Feb 27;9:315. doi: 10.3389/fmicb.2018.00315. eCollection 2018.
9
DrugBank 5.0: a major update to the DrugBank database for 2018.DrugBank 5.0:2018 年 DrugBank 数据库的重大更新。
Nucleic Acids Res. 2018 Jan 4;46(D1):D1074-D1082. doi: 10.1093/nar/gkx1037.
10
Subminimal inhibitory concentration (sub-MIC) of antibiotic induces electroactive biofilm formation in bioelectrochemical systems.抗生素的亚最小抑菌浓度(sub-MIC)会在生物电化学系统中诱导具有电活性的生物膜形成。
Water Res. 2017 Nov 15;125:280-287. doi: 10.1016/j.watres.2017.08.059. Epub 2017 Aug 29.