Porter Ned A, Xu Libin, Pratt Derek A
Department of Chemistry and Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, TN 37235, USA.
Department of Medicinal Chemistry, University of Washington, Seattle, WA 98195, USA.
Chemistry (Basel). 2020 Jun;2(2):390-417. doi: 10.3390/chemistry2020025. Epub 2020 May 6.
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.
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学研究的焦点。长期以来,脂质过氧化与炎症反应有关,最近,它被确定为称为铁死亡的氧化细胞死亡机制的核心原则。脂质亲电试剂-蛋白质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,但加合蛋白质的身份以及加合对蛋白质功能的影响大多未知。胆固醇和7-脱氢胆固醇(7-DHC,胆固醇的直接生物合成前体)都可被臭氧和以氧为中心的自由基等物质氧化。自由基链反应的产物混合物特别复杂,最近的研究扩展了所形成的亲电化合物的种类。在这里,我们描述了与甾醇衍生亲电试剂的形成以及这些亲电试剂与蛋白质的加合相关的最新进展。本综述介绍了近年来显著发展的理解甾醇过氧化机制的框架以及研究甾醇亲电试剂-蛋白质加合的方法。