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首页> 外文期刊>Methods: A Companion to Methods in Enzymology >Use of spin traps to detect superoxide production in living cells by electron paramagnetic resonance (EPR) spectroscopy
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Use of spin traps to detect superoxide production in living cells by electron paramagnetic resonance (EPR) spectroscopy

机译:使用旋转陷阱通过电子顺磁共振(EPR)光谱检测活细胞中的超氧化物生产

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摘要

Detection of superoxide produced by living cells has been an on-going challenge in biology for over forty years. Various methods have been proposed to address this issue, among which spin trapping with cyclic nitrones coupled to EPR spectroscopy, the gold standard for detection of radicals. This technique is based on the nucleophilic addition of superoxide to a diamagnetic cyclic nitrone, referred to as the spin trap, and the formation of a spin adduct, i.e. a persistent radical with a characteristic EPR spectrum. The first application of spin trapping to living cells dates back 1979. Since then, considerable improvements of the method have been achieved both in the structures of the spin traps, the EPR methodology, and the design of the experiments including appropriate controls. Here, we will concentrate on technical aspects of the spin trapping/EPR technique, delineating recent breakthroughs, inherent limitations, and potential artifacts. (C) 2016 Elsevier Inc. All rights reserved.
机译:通过生物细胞产生的超氧化物的检测在生物学超过四十多年来一直是对生物学的持续挑战。 已经提出了各种方法来解决该问题,其中旋转亚硝酸核苷酸与EPR光谱,用于检测基团的金标准。 该技术基于过氧化物的亲核加入到二磁环状亚硝酮,称为旋转阱,以及旋转加合物的形成,即具有特征EPR光谱的持续自由基。 旋转捕获到活细胞的第一次应用于1979年。从那时起,在旋转陷阱,EPR方法和实验的设计中,已经实现了该方法的大大改进,包括适当对照的实验的设计。 在这里,我们将专注于自旋捕获/ EPR技术的技术方面,划定近期突破,固有局限性和潜在伪影。 (c)2016年Elsevier Inc.保留所有权利。

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