用NAMD模拟脂氧合酶与花生四烯酸的相互作用

Zhongwei Li, E. Khosravi, Shuju Bai
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引用次数: 0

摘要

脂氧合酶(LOX)家族通过生物合成白三烯被认为是哮喘病理症状的主要原因。生理功能被认为是首先产生8R-HPETE(来源于花生四烯酸,简称AA),在进一步的酶促步骤中转化为白三烯。然而,关于5-Lox在炎症反应中的作用知之甚少。我们使用野生珊瑚脂氧合酶(8R-LOX)的1.85Å分辨率结构(41%的序列与人类花生四烯酸5-LOX相同)作为基础来模拟8R-LOX与其底物AA之间的相互作用,并使用ICM确定其结合位点。本研究对得到的8R-Lox:AA配合物进行了细化,并采用分子动力学方法(NAMD)进行了分析。利用VMD paratool插件开发了由一系列残基连接的非血红素铁未知结构的参数化方案。所有量子力学计算均采用Gaussian03进行,Becke3LYP泛函为6-31G (d)基集。
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Interaction simulation of Lipoxygenase with arachidonate acid using NAMD
Lipoxygenase (LOX) family is believed as the major cause of pathological symptoms in asthma by biosynthesis of leukotrienes. The physiological function is known as firstly producing 8R-HPETE (derived from arachidonate acid, referred as AA), which is transformed in further enzymatic step into leukotrienes. However, much less detail is known about the role of 5-Lox in the inflammatory reaction. We have used the 1.85Å resolution structure of a wild coral Lipoxygenase (8R-LOX) (with 41% sequence identical to the human arachidonate 5-LOX) as a foundation to model the interactions between 8R-Lox and its substrate AA, and its binding site was identified using ICM. In this research, the 8R-Lox:AA complex obtained was refined and analyzed by molecular dynamic method (NAMD). Parameterization scheme for unknown structure of non-heme iron ligated by a series of residues was developed using VMD paratool plugin. All quantum mechanical calculation were performed by Gaussian03 with the Becke3LYP functional at 6–31G(d) basis set.
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