Reactive Sterol Electrophiles: Mechanisms of Formation and Reactions with Proteins and Amino Acid Nucleophiles.

IF 2.4 Q3 CHEMISTRY, MULTIDISCIPLINARY Chemistry-Switzerland Pub Date : 2020-06-01 DOI:10.3390/chemistry2020025
Ned A Porter, Libin Xu, Derek A Pratt
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引用次数: 14

Abstract

Radical-mediated lipid oxidation and the formation of lipid hydroperoxides has been a focal point in the investigation of a number of human pathologies. Lipid peroxidation has long been linked to the inflammatory response and more recently, has been identified as the central tenet of the oxidative cell death mechanism known as ferroptosis. The formation of lipid electrophile-protein adducts has been associated with many of the disorders that involve perturbations of the cellular redox status, but the identities of adducted proteins and the effects of adduction on protein function are mostly unknown. Both cholesterol and 7-dehydrocholesterol (7-DHC), which is the immediate biosynthetic precursor to cholesterol, are oxidizable by species such as ozone and oxygen-centered free radicals. Product mixtures from radical chain processes are particularly complex, with recent studies having expanded the sets of electrophilic compounds formed. Here, we describe recent developments related to the formation of sterol-derived electrophiles and the adduction of these electrophiles to proteins. A framework for understanding sterol peroxidation mechanisms, which has significantly advanced in recent years, as well as the methods for the study of sterol electrophile-protein adduction, are presented in this review.

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反应性甾醇亲电试剂:形成机制及与蛋白质和氨基酸亲核试剂的反应。
自由基介导的脂质氧化和脂质氢过氧化物的形成一直是许多人类病理研究的焦点。脂质过氧化长期以来一直与炎症反应有关,最近已被确定为氧化细胞死亡机制的核心原则,即铁下垂。脂类亲电蛋白加合物的形成与许多涉及细胞氧化还原状态扰动的疾病有关,但加合蛋白的特性以及加合对蛋白质功能的影响大多是未知的。胆固醇和7-脱氢胆固醇(7-DHC)都可被臭氧和氧中心自由基等物质氧化。7-DHC是胆固醇的直接生物合成前体。自由基链反应的产物混合物特别复杂,最近的研究扩大了形成的亲电化合物的集合。在这里,我们描述了与固醇衍生的亲电试剂的形成和这些亲电试剂对蛋白质的内聚有关的最新进展。本文综述了近年来对甾醇过氧化机制的研究进展,以及甾醇亲电-蛋白内合反应的研究方法。
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来源期刊
Chemistry-Switzerland
Chemistry-Switzerland CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.20
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0.00%
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0
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hERG Blockade Prediction by Combining Site Identification by Ligand Competitive Saturation and Physicochemical Properties. The Non-Anhydrous, Minimally Basic Synthesis of the Dopamine D2 Agonist [18F]MCL-524. Reactive Sterol Electrophiles: Mechanisms of Formation and Reactions with Proteins and Amino Acid Nucleophiles.
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