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首页> 外文期刊>Journal of the American Society for Mass Spectrometry >Extensive Charge Reduction and Dissociation of Intact Protein Complexes Following Electron Transfer on a Quadrupole-Ion Mobility-Time-of-Flight MS
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Extensive Charge Reduction and Dissociation of Intact Protein Complexes Following Electron Transfer on a Quadrupole-Ion Mobility-Time-of-Flight MS

机译:在四极离子淌度飞行时间质谱仪上进行电子转移后,完整蛋白质复合物的大量电荷减少和解离

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摘要

Non-dissociative charge reduction, typically considered to be an unwanted side reaction in electron transfer dissociation (ETD) experiments, can be enhanced significantly in order to reduce the charge state of intact protein complexes to as low as 1+ on a commercially available Q-IM-TOF instrument. This allows for the detection of large complexes beyond 100,000 m/z, while at the same time generating top-down ETD fragments, which provide sequence information from surface-exposed parts of the folded structure. Optimization of the supplemental activation has proven to be crucial in these experiments and the charge-reduced species are most likely the product of both proton transfer (PTR) and non-dissociative electron transfer (ETnoD) reactions that occur prior to the ion mobility cell. Applications of this approach range from deconvolution of complex spectra to the manipulation of charge states of gas-phase ions.
机译:非解离电荷减少通常被认为是电子转移解离(ETD)实验中不希望有的副反应,为了使完整蛋白质复合物的电荷状态在市售Q-上降低至低至1+,可以显着提高非解离电荷减少IM-TOF仪器。这允许检测超过100,000 m / z的大型复合物,同时生成自上而下的ETD片段,该片段提供来自折叠结构的表面暴露部分的序列信息。在这些实验中,补充活化的优化已被证明是至关重要的,而减少电荷的物质极有可能是在离子迁移池之前发生的质子转移(PTR)和非离解电子转移(ETnoD)反应的产物。这种方法的应用范围从复杂光谱的去卷积到气相离子电荷状态的操纵。

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