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On-tissue Direct Monitoring of Global Hydrogen/Deuterium Exchange by MALDI Mass Spectrometry: Tissue Deuterium Exchange Mass Spectrometry (TDXMS)

机译:通过MALDI质谱对组织中的氢/氘交换进行直接监测:组织氘交换质谱(TDXMS)

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摘要

Hydrogen/deuterium exchange mass spectrometric (H/DXMS) methods for protein structural analysis are conventionally performed in solution. We present Tissue Deuterium Exchange Mass Spectrometry (TDXMS), a method to directly monitor deuterium uptake on tissue, as a means to better approximate the deuterium exchange behavior of proteins in their native microenvironment. Using this method, a difference in deuterium uptake behavior was observed when the same proteins were monitored in solution and on tissue. The higher maximum deuterium uptake at equilibrium for all proteins analyzed in solution suggests a more open conformation in the absence of interacting partners normally observed on tissue. We also demonstrate a difference in the deuterium uptake behavior of a few proteins across different morphological regions of the same tissue section. Modifications of the total number of hydrogens exchanged, as well as the kinetics of exchange, were both observed. These results provide information on the implication of protein interactions with partners as well as on the conformational changes related to these interactions, and illustrate the importance of examining protein deuterium exchange behavior in the presence of its specific microenvironment directly at the level of tissues.
机译:蛋白质结构分析的氢/氘交换质谱法(H / DXMS)通常在溶液中进行。我们提出组织氘交换质谱法(TDXMS),一种直接监测组织上氘的摄取的方法,以更好地近似其天然微环境中蛋白质的氘交换行为。使用这种方法,当在溶液中和组织上监测相同的蛋白质时,观察到氘的吸收行为有所不同。在溶液中分析的所有蛋白质在平衡状态下较高的最大氘吸收量表明在缺乏通常在组织上观察到的相互作用伴侣的情况下,构象更为开放。我们还证明了在相同组织切片的不同形态区域中,几种蛋白质的氘吸收行为存在差异。均观察到交换的氢总数的变化以及交换的动力学。这些结果提供了有关蛋白质与伴侣之间相互作用的含义以及与这些相互作用有关的构象变化的信息,并说明了直接在组织水平上检查存在特定微环境的蛋白质氘交换行为的重要性。

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