Departamento de Bioquímica, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay; Center for Free Radical and Biomedical Research, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Departamento de Bioquímica, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay; Center for Free Radical and Biomedical Research, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Free Radic Biol Med. 2018 Nov 20;128:59-68. doi: 10.1016/j.freeradbiomed.2018.02.017. Epub 2018 Feb 15.
In the last two decades, there has been a significant advance in understanding the biochemistry of peroxynitrite, an endogenously-produced oxidant and nucleophile. Its relevance as a mediator in several pathologic states and the aging process together with its transient character and low steady-state concentration, motivated the development of a variety of techniques for its unambiguous detection and estimation. Among these, fluorescence and chemiluminescence approaches have represented important tools with enhanced sensitivity but usual limited specificity. In this review, we analyze selected examples of molecular probes that permit the detection of peroxynitrite by fluorescence and chemiluminescence, disclosing their mechanism of reaction with either peroxynitrite or peroxynitrite-derived radicals. Indeed, probes have been divided into 1) redox probes that yield products by a free radical mechanism, and 2) electrophilic probes that evolve to products secondary to the nucleophilic attack by peroxynitrite. Overall, boronate-based compounds are emerging as preferred probes for the sensitive and specific detection and quantitation. Moreover, novel strategies involving genetically-modified fluorescent proteins with the incorporation of unnatural amino acids have been recently described as peroxynitrite sensors. This review analyzes the most commonly used fluorescence and chemiluminescence approaches for peroxynitrite detection and provides some guidelines for appropriate experimental design and data interpretation, including how to estimate peroxynitrite formation rates in cells.
在过去的二十年中,人们对内源性氧化剂和亲核试剂过氧亚硝酸盐的生物化学有了重大的认识进展。由于它作为几种病理状态和衰老过程中介的相关性,以及其瞬态特征和低稳态浓度,促使人们开发了各种明确检测和估计过氧亚硝酸盐的技术。其中,荧光和化学发光方法已成为具有增强灵敏度但通常特异性有限的重要工具。在这篇综述中,我们分析了允许通过荧光和化学发光检测过氧亚硝酸盐的分子探针的一些示例,揭示了它们与过氧亚硝酸盐或过氧亚硝酸盐衍生自由基反应的机制。实际上,探针已分为 1)通过自由基机制产生产物的氧化还原探针,和 2)通过亲核攻击过氧亚硝酸盐而演变出产物的亲电探针。总体而言,硼酸基化合物作为灵敏和特异检测及定量过氧亚硝酸盐的首选探针而崭露头角。此外,最近还描述了涉及基因修饰的荧光蛋白与非天然氨基酸的掺入的新型策略,作为过氧亚硝酸盐传感器。本文分析了最常用的荧光和化学发光方法用于过氧亚硝酸盐检测,并提供了一些关于适当实验设计和数据解释的指导原则,包括如何估计细胞中过氧亚硝酸盐的形成速率。