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Charge-state Resolved Infrared Multiple Photon Dissociation (IRMPD) Spectroscopy of Ubiquitin Ions in the Gas Phase

机译:气相泛素离子的电荷态分辨红外多光子离解(IRMPD)光谱

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摘要

In this study, we obtained for the first time the direct infrared multiple photon dissociation (IRMPD) spectra of ubiquitin ions in the range 2700–3750 cm−1. Ubiquitin ions with different charge states showed absorption in the two regions of 2940–3000 cm−1 and 3280–3400 cm−1. The increase of the charge state of ubiquitin ions broadened the absorption peak on the high-frequency side in the second region, indicating some hydrogen bonds were weakened due to Coulomb interaction. It is also found that the relative intensity of the absorption peak in the first region compared to the absorption peak in the second region increased with increasing charge state, making the IRMPD spectra charge-state resolved. Although it is usually reasonable to suggest the origin of the absorption in the range 2940–3000 cm−1 as the C-H bond stretching modes, the results show significantly reduced absorption after the deuteration of all labile hydrogen atoms. A possible explanation for this is that the coupling coefficients between the C-H vibrational mode and other selective modes decreased greatly after the deuteration, reducing the rate of energy redistribution and probability of consecutive IR absorption.
机译:在本研究中,我们首次获得了泛素离子在2700–3750 cm -1 范围内的直接红外多光子离解(IRMPD)光谱。具有不同电荷状态的泛素离子在2940–3000 cm -1 和3280–3400 cm -1 两个区域显示吸收。泛素离子的电荷态的增加使第二区域中高频侧的吸收峰变宽,表明一些氢键由于库仑相互作用而被削弱。还发现,与第二区域中的吸收峰相比,第一区域中的吸收峰的相对强度随着电荷态的增加而增加,从而使IRMPD光谱的电荷态分解。尽管通常合理地建议吸收的起源为C-H键拉伸模式,其吸收范围为2940–3000 cm -1 ,但结果表明,在所有不稳定的氢原子氘化后,吸收显着降低。对此的可能解释是,氘化后C-H振动模式与其他选择模式之间的耦合系数大大降低,从而降低了能量重新分配的速度和连续IR吸收的可能性。

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