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A selective and sensitive method for quantification of endogenous polysulfide production in biological samples

机译:一种选择性灵敏的生物样品中内生多硫化物产量定量方法

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摘要

Hydrogen sulfide (H2S) is a gasotransmitter that regulates cellular homeostasis and impacts on multiple physiological and pathophysiological processes. However, it exerts many of its biological actions indirectly via the formation of H2S-derived sulfane sulfur species/polysulfides. Because of the high reactivity of sulfur species, the detection of H2S-derived polysulfides in biological systems is challenging and currently used methods are neither sensitive nor quantitative. Herein, we describe a LC-MS/MS-based method that makes use of Sulfane Sulfur Probe 4 to detect endogenously generated polysulfides in biological samples in a selective, sensitive and quantitative manner. The results indicate a large variability in the activity of the H2S-generating enzymes in different murine organs, but the method described was able to detect intracellular levels of polysulfides in the nanomolar range and identify cystathionine γ-lyase as the major intracellular source of sulfane sulfur species/polysulfides in murine endothelial cells and hearts. The protocol described can be applied to a variety of biological samples for the quantification of the H2S-derived polysulfides and has the potential to increase understanding on the control and consequences of this gaseous transmitter.
机译:硫化氢(H2S)是一种气体递质,可调节细胞体内稳态并影响多种生理和病理生理过程。但是,它通过形成H2S衍生的亚砜硫物种/多硫化物间接发挥其许多生物学作用。由于硫物种的高反应活性,在生物系统中检测H2S衍生的多硫化物具有挑战性,当前使用的方法既不灵敏也不定量。在本文中,我们描述了一种基于LC-MS / MS的方法,该方法利用硫磺硫探针4以选择性,灵敏和定量的方式检测生物样品中内生的多硫化物。结果表明不同鼠器官中生成H2S的酶的活性差异很大,但是所描述的方法能够检测纳摩尔浓度范围内的多硫化物的细胞内水平,并确定胱硫醚γ-裂合酶是硫丹的主要细胞内来源鼠内皮细胞和心脏中的物种/多硫化物。可以将所描述的方案应用于各种生物样品中,以量化H2S衍生的多硫化物,并有可能增进人们对该气体变送器的控制和后果的了解。

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