首页> 外文期刊>International Journal of Molecular Sciences >An Advanced Electron Spin Resonance (ESR) Spin-Trapping and LC/(ESR)/MS Technique for the Study of Lipid Peroxidation
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An Advanced Electron Spin Resonance (ESR) Spin-Trapping and LC/(ESR)/MS Technique for the Study of Lipid Peroxidation

机译:脂质过氧化研究的高级电子自旋共振(ESR)自旋俘获和LC /(ESR)/ MS技术

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摘要

There are two types of nutritionally important polyunsaturated fatty acids (PUFAs), namely ω-6s and ω-3s. PUFAs and their metabolites generated from lipid peroxidation via cyclooxygenase (COX) and lipoxygenase (LOX) are believed to be involved in a variety of physiological and pathological processes in the human body. Both COX- and LOX-catalyzed PUFA peroxidation are complex events that generate a series of radicals, which may then bind proteins, target DNA/RNA, and lead to a number of biological changes. However, due to the lack of an appropriate method, it was not possible until recently to identify the short-lived PUFA-derived radicals in COX-/LOX-catalyzed peroxidation. Failure to characterize free radicals during peroxidation has greatly restricted our knowledge about COX/LOX biology in human health. Here we review the development and refinement of combined ESR spin trapping and LC/ESR/MS to characterize PUFA-derived radicals formed from in vitro (cell-free) peroxidation. We also present the most recent approach for studying peroxidation in cells which allows us to directly assess the potential bioactivity of PUFA-derived free radicals. This advanced technique has resulted in a major breakthrough in radical structural characterization, as well as assessment of free radical-associated cell growth response, thereby greatly improving our knowledge of PUFAs, COX-/LOX-catalyzed lipid peroxidation, and their related biological consequences.
机译:营养上重要的多不饱和脂肪酸(PUFA)有两种类型,即ω-6和ω-3。经由环加氧酶(COX)和脂氧合酶(LOX)由脂质过氧化作用产生的PUFA及其代谢物被认为与人体的各种生理和病理过程有关。 COX和LOX催化的PUFA过氧化都是复杂的事件,它们产生一系列自由基,这些自由基随后可以结合蛋白质,靶向DNA / RNA,并导致许多生物学变化。然而,由于缺乏合适的方法,直到最近才能够在COX / LOX催化的过氧化反应中鉴定短寿命的PUFA衍生的自由基。在过氧化过程中无法表征自由基,极大地限制了我们对人类健康中COX / LOX生物学的了解。在这里,我们审查结合ESR自旋阱和LC / ESR / MS的发展和完善,以表征由体外(无细胞)过氧化作用形成的PUFA衍生的自由基。我们还提出了研究细胞中过氧化反应的最新方法,这使我们能够直接评估PUFA衍生的自由基的潜在生物活性。这项先进的技术在自由基结构表征以及评估自由基相关细胞生长反应方面取得了重大突破,从而大大提高了我们对PUFA,COX / LOX催化脂质过氧化及其相关生物学后果的认识。

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