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SMALL NEUTRAL LOSSES IN THE ELECTRON CAPTURE DISSOCIATION OF NITRATED PEPTIDES

机译:氮化肽的电子捕获解离中的小中性损失

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In vivo protein nitration is associated with many disease conditions that involve oxidative stress and inflammatory response. Nitration occurs at tyrosine residues. In order to understand the mechanisms and consequences of protein nitration, it is necessary to identify nitrotyrosine-containing proteins and to localize the sites of modification. We have previously shown that the presence of 3-nitrotyrosine within a peptide sequence has a deleterious effect on electron capture dissociation (ECD) backbone cleavage [1]. That effect is particularly severe for doubly-charged precursor ions, and can be explained by the 'electron predator' model proposed by Beauchamp and co-workers [2].
机译:体内蛋白质硝化与许多涉及氧化应激和炎症反应的疾病病症有关。硝化在酪氨酸残留物中发生。为了理解蛋白质硝化的机制和后果,有必要鉴定含硝基甲酰胺的蛋白质并定位改性位点。我们之前表明,在肽序列中存在3-硝基曲霉对电子捕获解离(ECD)骨架裂解的有害影响[1]。这种效果对于双电荷的前体离子特别严重,并且可以通过Beauchamp和Co-Worker提出的“电子捕食者”模型来解释[2]。

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