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一种采用分子对接和分子动力学模拟的免疫信息学方法,用于评估由……产生的L-天冬酰胺酶。 (注:原文句末不完整)

An immunoinformatic approach employing molecular docking and molecular dynamics simulation for evaluation of l-asparaginase produced by .

作者信息

Hozoorbakhsh Fereshteh, Ghiasian Mozhgan, Ghandehari Fereshte, Emami-Karvani Zarrindokht, Khademi Dehkordi Maryam

机构信息

Department of Microbiology, Falavarjan Branch, Islamic Azad University, Isfahan, Iran.

Department of Biology, Falavarjan Branch, Islamic Azad University, Isfahan, Iran.

出版信息

J Biomol Struct Dyn. 2023 Oct-Nov;41(18):9057-9071. doi: 10.1080/07391102.2022.2139765. Epub 2022 Nov 15.

DOI:10.1080/07391102.2022.2139765
PMID:36377397
Abstract

l-Asparaginase is one of the most important treatments for acute lymphoblastic leukemia. In this study, l-asparaginase-producing bacteria were isolated from the effluent and soil of the Isfahan slaughterhouse using M9 specific medium. Isolates were identified by 16SrRNA phylogenetic analysis. The immune characteristics were predicted. Molecular docking was performed between l-asparaginase and l-asparagine substrate using AutoDock tools 4.2 and AutoDock Vina. Molecular dynamics simulation studies were fulfilled using GROMACS. Five l-asparaginase-producing bacteria isolated that belonging to , sp. , and . Predictions showed has better immune characteristics than . The binding energies of the docked complex were calculated to be -4.34 and -4.9 kcal/mol. Molecular docking confirmed the interaction of l-asparaginase with its substrate. It was observed that the residues Thr36, Tyr50, Ala47, Thr116, Asp117, Met142, Thr193 and Thr192 were fundamental in protein-ligand complexation. Also, RMSD, RMSF, Rg, DSSP, SASA and MM-PBSA analysis showed that when l-asparaginase is bound to l-asparagine, it did not lose stability, secondary structure and compactness. Slaughterhouse soils and effluents are a potential source of l-asparaginase-producing bacteria that probably can probably produce l-asparaginase with more favorable immune properties than commercial enzymes.Communicated by Ramaswamy H. Sarma.

摘要

L-天冬酰胺酶是急性淋巴细胞白血病最重要的治疗方法之一。在本研究中,使用M9特异性培养基从伊斯法罕屠宰场的废水和土壤中分离出产L-天冬酰胺酶的细菌。通过16SrRNA系统发育分析对分离株进行鉴定。预测其免疫特性。使用AutoDock tools 4.2和AutoDock Vina对L-天冬酰胺酶和L-天冬酰胺底物进行分子对接。使用GROMACS进行分子动力学模拟研究。分离出五株产L-天冬酰胺酶的细菌,分别属于 、 属、 属和 属。预测表明 具有比 更好的免疫特性。对接复合物的结合能计算为-4.34和-4.9千卡/摩尔。分子对接证实了L-天冬酰胺酶与其底物的相互作用。观察到Thr36、Tyr50、Ala47、Thr116、Asp117、Met142、Thr193和Thr192残基在蛋白质-配体络合中起重要作用。此外,RMSD、RMSF、Rg、DSSP、SASA和MM-PBSA分析表明,当L-天冬酰胺酶与L-天冬酰胺结合时,它不会失去稳定性、二级结构和紧密性。屠宰场的土壤和废水是产L-天冬酰胺酶细菌的潜在来源,这些细菌可能产生比商业酶具有更有利免疫特性的L-天冬酰胺酶。由拉马斯瓦米·H·萨尔马传达。

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