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肽中氧化甲硫氨酸的鉴定。

Identification of oxidized methionine in peptides.

作者信息

Lagerwerf F M, van de Weert M, Heerma W, Haverkamp J

机构信息

Bijvoet Center for Biomolecular Research, Department of Mass Spectrometry, Utrecht University, The Netherlands.

出版信息

Rapid Commun Mass Spectrom. 1996;10(15):1905-10. doi: 10.1002/(SICI)1097-0231(199612)10:15<1905::AID-RCM755>3.0.CO;2-9.

Abstract

The positive- and negative-ion collision-induced dissociation spectra of peptides containing methionine, methionine sulphoxide and methionine sulphone have been studied. Characteristic fragmentations were identified and evaluated as possible indicators for the presence of oxidized methionine residues in peptides. It was found that the elimination of CH3SOH (-64 u) from [M + H]+ is unique for peptides that contain methionine sulphoxide. Sequence ions containing the oxidized methionine undergo the same elimination, allowing unambiguous sequence determination. Methionine sulphone exhibits an analogous elimination of CH3SO2H (-80 u) from the protonated molecule, but not from sequence ions.

摘要

对含有甲硫氨酸、甲硫氨酸亚砜和甲砜的肽的正离子和负离子碰撞诱导解离光谱进行了研究。鉴定并评估了特征性碎裂,将其作为肽中氧化甲硫氨酸残基存在的可能指标。发现从[M + H]+中消除CH3SOH(-64 u)是含有甲硫氨酸亚砜的肽所特有的。含有氧化甲硫氨酸的序列离子会发生相同的消除反应,从而能够明确确定序列。甲砜在质子化分子中表现出类似的消除CH3SO2H(-80 u)的反应,但在序列离子中则不会。

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