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Quantitation of Reactive Acyl-CoA Species Mediated Protein Acylation by HPLC-MS/MS

机译:通过HPLC-MS / MS进行反应性酰基-CoA物种的定量介导的蛋白质酰化

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摘要

Recently discovered acylation by reactive acyl-CoA species is considered a novel regulatory mechanism in epigenetics and metabolism. Established analytical methods like Western blotting and proteomics fail to detect the plethora of acylation structures in a single analysis and lack the ability of absolute quantitation. In this paper, we developed an HPLC-MS/MS method for the simultaneous detection and quantitation of 14 acylated lysine species in biological samples. Extensive effort was invested into method validation resulting in recovery rates between 75 and 93% and levels of detection in the nanomolar range. Thus, we were able to quantitate 8 acylation structures in mouse liver, kidney, heart, and brain. Further enrichment by repetitive HPLC fractionation resulted in the quantitation of 6 additional acylation structures including 4 novel modifications: N-6-acetoacetyl lysine, N-6-isovaleryl lysine, N-6-(2-methylbutyryl) lysine, and N-6-tiglyl lysine.
机译:最近发现反应性酰基-CoA物种的酰化被认为是表观遗传学和代谢的新调节机制。 已建立的分析方法,如蛋白质观和蛋白质组学,在单一分析中不能检测到丙烯化结构的血清化结构,缺乏绝对定量的能力。 在本文中,我们开发了一种HPLC-MS / MS方法,用于在生物样品中同时检测和定量14种酰化赖氨酸物种。 广泛的努力投入了方法验证,导致75至93%之间的回收率和纳米摩尔范围内的检测水平。 因此,我们能够定量小鼠肝,肾,心脏和脑中的8个酰化结构。 通过重复性HPLC分级的进一步富集导致6另外的酰化结构的定量,包括4个新型修饰:N-6-乙酰乙酰赖氨酸,N-6-异戊酸赖氨酸,N-6-(2-甲基丁基)赖氨酸和N-6- 蒂格利赖氨酸。

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  • 来源
    《Analytical chemistry》 |2019年第19期|共8页
  • 作者单位

    Martin Luther Univers Halle Wittenberg Food Chem Inst Chem Kurt Mothes Str 2 D-06120 Halle Saale Germany;

    FLI Leibniz Inst Aging Beutenbergstr 11 D-07745 Jena Germany;

    FLI Leibniz Inst Aging Beutenbergstr 11 D-07745 Jena Germany;

    Martin Luther Univers Halle Wittenberg Food Chem Inst Chem Kurt Mothes Str 2 D-06120 Halle Saale Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
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