次卤酸与蛋白质的比较反应性:化学、生物效应和后果

Els A. Hartsema , Helen Hemmling , Clare L. Hawkins
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引用次数: 0

摘要

次卤酸(HOX)是由不同的哺乳动物血红素过氧化物酶产生的化学氧化剂,可被激活的免疫细胞释放。这些氧化剂在先天免疫中发挥重要作用,因为它们能够迅速杀死和解毒病原体。然而,由于许多炎症病理中免疫细胞的丰富和过度激活,HOX也与驱动宿主组织损伤有关。蛋白质在生物系统中非常丰富,是HOX的关键靶点。这些反应导致氨基酸侧链的修饰,以及蛋白质的展开、断裂和聚集,具有显著的结构和功能效应。这导致了一项重要的研究工作,重点是获得有关hox诱导的蛋白质损伤的分子机制的详细了解,以及它如何促进疾病的进展和死亡。本文综述了HOX与蛋白质的反应性,包括特定氨基酸残基修饰的机制,以及这如何促进结构和功能的变化。我们描述了HOX修饰蛋白质导致疾病的潜在途径,并概述了一些在治疗上调节这种损伤的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative reactivity of hypohalous acids with proteins: Chemistry, biological effects and consequences
Hypohalous acids (HOX) are chemical oxidants that are produced by different mammalian heme peroxidases, which can be released by activated immune cells. These oxidants play an important role in innate immunity, owing to their ability to rapidly kill and detoxify pathogens. However, HOX are also implicated in driving host tissue damage, due to the abundance and over-activation of immune cells in many inflammatory pathologies. Proteins are highly abundant in biological systems and constitute key targets for HOX. These reactions lead to the modification of amino acid side chains, together with protein unfolding, fragmentation and aggregation, which have significant structural and functional effects. This has led to a significant research effort focused on gaining a detailed understanding of the molecular mechanisms involved in HOX-induced protein damage, and how it contributes to the progression of disease and mortality. This review describes the reactivity of HOX with proteins, including the mechanisms involved in the modification of specific amino acid residues, and how this contributes to structural and functional changes. We describe potential pathways by which modification of proteins by HOX contribute to disease and outline some strategies to modulate this type of damage therapeutically.
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来源期刊
CiteScore
2.60
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