Characterisation of hydrophobic interactions of ubiquinol with AtAOX and EsAOX isoforms by site-directed mutagenesis, molecular dynamics and docking.

IF 2.5 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Varsha Venugopalan, Rajesh Parsanathan, Dinakar Challabathula, Kavya Bakka
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引用次数: 0

Abstract

Alternative oxidase (AOX) is cyanide insensitive terminal oxidase of plant mitochondrial electron transport chain serving as important bypass from classical cytochrome pathway for reduction in generation of reactive oxygen species (ROS) and for maintenance of redox homeostasis under diverse stress conditions. While many studies have emphasised on AOX structure in premature form, the mitochondria localised mature form which is biologically relevant for substrate interaction is not much explored. In the current study, we have performed comparative structural and molecular docking analysis of mature AOX isoforms from stress-sensitive Arabidopsis thaliana and extremophile Eutrema salsugineum to elucidate molecular determinants of ubiquinol binding and stress tolerance. Homology models of AOX isoforms were constructed and validated through SWISS-MODEL, GalaxyWEB, and Ramachandran plot. Docking of activators (pyruvate, glyoxylate, oxaloacetate, 2-oxoglutarate) and substrate (ubiquinol) revealed strong hydrophobic interactions, predominantly Pi-Pi alkyl bonds, within conserved catalytic domains. Among all isoforms, AtAOX1a and EsAOX1a exhibited highest binding affinities with ubiquinol. In-silico site-directed mutagenesis and molecular dynamics simulations demonstrated that substitution of conserved hydrophobic residues, Val184 in AtAOX1a and Val118 in EsAOX1a, with aspartic acid (V→D) did not alter structural stability but significantly disrupted ubiquinol-binding pocket and reduced binding affinity indicating conserved valine residues as hydrophobic anchors crucial for substrate stabilisation. The study underscores hydrophobic interactions as key determinant of AOX function proposing valine as potential site for in-vitro mutagenesis to modulate AOX-mediated stress responses. The findings serve as foundation for future experimental studies addressing AOX mediated stress responses and exploring strategies for improving plant stress tolerance.

泛醇与AtAOX和EsAOX异构体疏水相互作用的位点定向诱变、分子动力学和对接表征。
替代氧化酶(Alternative oxidase, AOX)是植物线粒体电子传递链上对氰化物不敏感的末端氧化酶,是植物在不同胁迫条件下减少活性氧(ROS)生成和维持氧化还原稳态的重要旁路途径。虽然许多研究都强调过早形式的AOX结构,但与底物相互作用相关的线粒体局部成熟形式的探索并不多。在目前的研究中,我们对胁迫敏感的拟南芥和极端微生物Eutrema salsugineum的成熟AOX异构体进行了比较结构和分子对接分析,以阐明泛醇结合和胁迫耐受性的分子决定因素。通过SWISS-MODEL、GalaxyWEB和Ramachandran图构建并验证AOX同型异构体的同源性模型。激活剂(丙酮酸酯、乙醛酸酯、草酰乙酸酯、2-氧戊二酸酯)与底物(泛醇)的对接显示出在保守的催化区域内强烈的疏水相互作用,主要是Pi-Pi烷基键。在所有亚型中,AtAOX1a和EsAOX1a与泛醇的结合亲和力最高。硅基定向诱变和分子动力学模拟表明,用天冬氨酸(V→D)取代保守的疏水残基AtAOX1a中的Val184和EsAOX1a中的Val118不会改变结构稳定性,但会显著破坏泛醇结合囊并降低结合亲和力,这表明保守的缬氨酸残基是对底物稳定至关重要的疏水锚。该研究强调疏水相互作用是AOX功能的关键决定因素,建议缬氨酸作为体外诱变的潜在位点来调节AOX介导的应激反应。该研究结果为进一步研究AOX介导的胁迫反应和探索植物抗逆性策略奠定了基础。
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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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