Investigating anti-inflammatory actions of marine algal compound against lipoxygenase concentrating on therapeutic applications through computational approach.

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biomolecular Structure & Dynamics Pub Date : 2024-10-01 Epub Date: 2023-08-29 DOI:10.1080/07391102.2023.2249115
Akanksha Dubey, Jayanthi Sivaraman
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Abstract

Inflammation is the preliminary response given to any possible harmful stimuli including infections, injury or stress by immune system where neutrophils and macrophages gets activated and produces mediators, such as nitric oxide and cytokines that serves as biomarkers of inflammation. Lipoxygenases are enzymes that peroxidises lipids and are involved in the pathogenesis of several diseases including inflammatory diseases. These are oxidative enzymes comprising a non-heme iron atom in active site and are convoluted in inflammatory reactions. Fucoidan is sulphated polysaccharide that has numerous pharmacological implications. Implications of fucoidan on inflammatory diseases are still an objective of rigorous research. Therefore, this study focusses on investigating lipoxygenase inhibitory activities of fucoidan. The mechanism of lipoxygenase inhibitory activities of fucoidan was studied via molecular docking and molecular dynamics simulations. The docking score produced by the binding of the fucoidan to the lipoxygenase was - 6.69 kcal/mol whereas, the docking score in case of Aspirin and Zileuton were -5.8 kcal/mol and -7.0 kcal/mol and it was found that fucoidan makes hydrogen bonds with lipoxygenase protein through polar amino acid glutamine at GLN 514. The results obtained from molecular dynamics simulations proposed the development of a stable complex between fucoidan and lipoxygenase due to the establishment of favourable interactions with amino acid residues and indicated efficient results when compared with Aspirin and Zileuton. This study suggested that fucoidan had anti-inflammatory potentials and thus can be used as a promising drug candidate against inflammation.Communicated by Ramaswamy H. Sarma.

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通过计算方法研究海洋藻类化合物对脂氧合酶的抗炎作用,集中于治疗应用。
炎症是免疫系统对任何可能的有害刺激(包括感染、损伤或压力)做出的初步反应,中性粒细胞和巨噬细胞在此过程中被激活,并产生一氧化氮和细胞因子等介质,作为炎症的生物标志物。脂氧合酶是一种能使脂质过氧化的酶,与包括炎症性疾病在内的多种疾病的发病机制有关。这些氧化酶的活性位点含有一个非血红素铁原子,在炎症反应中起着重要作用。褐藻糖胶是一种硫酸化多糖,具有多种药理作用。褐藻糖胶对炎症性疾病的影响仍是严谨研究的目标。因此,本研究重点研究褐藻糖胶的脂氧合酶抑制活性。通过分子对接和分子动力学模拟研究了褐藻糖胶抑制脂氧合酶活性的机制。褐藻糖胶与脂氧合酶结合产生的对接分数为-6.69 kcal/mol,而阿司匹林和齐鲁通的对接分数分别为-5.8 kcal/mol 和-7.0 kcal/mol。分子动力学模拟的结果表明,由于褐藻糖胶与氨基酸残基建立了有利的相互作用,褐藻糖胶与脂氧合酶之间形成了稳定的复合物,与阿司匹林和齐鲁通相比,效果显著。这项研究表明,褐藻糖胶具有抗炎潜力,因此可作为一种有前途的抗炎候选药物。
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来源期刊
Journal of Biomolecular Structure & Dynamics
Journal of Biomolecular Structure & Dynamics 生物-生化与分子生物学
CiteScore
8.90
自引率
9.10%
发文量
597
审稿时长
2 months
期刊介绍: The Journal of Biomolecular Structure and Dynamics welcomes manuscripts on biological structure, dynamics, interactions and expression. The Journal is one of the leading publications in high end computational science, atomic structural biology, bioinformatics, virtual drug design, genomics and biological networks.
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