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Fragmentation of phosphorylated and singly charged peptide ions via interaction with metastable atoms

机译:通过与亚稳原子的相互作用使磷酸化和单电荷的肽离子断裂

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摘要

Fragmentation of phosphorylated peptide ions via interaction with electronically excited metastable argon atoms was studied in a linear trap – time-of-flight mass spectrometer. Doubly charged ions of phosphorylated peptides from an Enolase digest were produced by electrospray ionization and subjected to a metastable atom beam in the linear trap. The metastable argon atoms were generated using a glow-discharge source. An intensive series of c- and z- ions were observed in all cases, with the phosphorylation group intact. The formation of molecular radical cations with reduced charge indicated that an electron transfer from a highly excited metastable state of argon to the peptide cation occurred. Additionally, singly charged Bradykinin, Substance P and Fibrinopeptide A molecular ions were fragmented via interaction with electronically excited metastable helium atoms. The fragmentation mechanism was different in this case and involved Penning ionization.
机译:在线性阱-飞行时间质谱仪中研究了通过与电子激发的亚稳态氩原子相互作用而使磷酸化的肽离子碎裂。来自烯醇酶消化物的磷酸化肽的双电荷离子通过电喷雾电离产生,并在线性阱中受到亚稳原子束的作用。使用辉光放电源产生亚稳氩原子。在所有情况下均观察到一系列强烈的c和z离子,且磷酸化基团完好无损。带有减少电荷的分子自由基阳离子的形成表明发生了电子从氩的高度激发的亚稳态转移到肽阳离子的过程。此外,单电荷缓激肽,P物质和纤维蛋白肽A分子离子通过与电子激发的亚稳态氦原子相互作用而破碎。在这种情况下,碎裂机理是不同的,涉及潘宁电离。

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