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通过离子Z态操纵实现前体解析:一种用于分析多电荷离子混合物的串联质谱方法。

Precursor Resolution via Ion Z-State Manipulation: A Tandem Mass Spectrometry Approach for the Analysis of Mixtures of Multiply-Charged Ions.

作者信息

Pizzala Nicolas J, Chao Hsi-Chun, Faye Boukar K S, McLuckey Scott A

机构信息

Department of Chemistry, Purdue University, West Lafayette, Indiana, USA.

Beckman Institute for Advanced Science and Technology, University of Illinois, Urbana-Champaign, Illinois, USA.

出版信息

J Mass Spectrom. 2025 May;60(4):e5124. doi: 10.1002/jms.5124.

DOI:10.1002/jms.5124
PMID:40159668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11955721/
Abstract

Electrospray ionization (ESI) is often the ionization method of choice, particularly for high-mass polar molecules and complexes. However, when analyzing mixtures of analytes, charge state ambiguities and overlap in mass-to-charge (m/z) can arise from species with different masses and charges. While solution-phase conditions can sometimes be optimized to produce relatively low charge states-thereby reducing charge-state ambiguity and m/z overlap-gas-phase methods offer greater control over charge state reduction. For complex mixtures, however, charge state reduction alone often fails to resolve individual components in the mixture. Incorporating a mass-selection step prior to charge state manipulation can simplify the mixture and significantly improve the separation of the components. This general tandem mass spectrometry approach is referred to here as precursor resolution via ion z-state manipulation (PRIZM). Examples of variations of PRIZM experiments date back roughly 25 years and have involved ion/molecule proton transfer reactions, ion/ion proton transfer reactions, ion/ion electron transfer reactions, electron capture reactions, and multiply-charged ion attachment reactions. This tutorial review describes the PRIZM approach and provides illustrative examples using each of the charge state manipulation approaches mentioned above.

摘要

电喷雾电离(ESI)通常是首选的电离方法,特别是对于高质量的极性分子和复合物。然而,在分析分析物混合物时,不同质量和电荷的物种可能会导致电荷状态的模糊性以及质荷比(m/z)的重叠。虽然有时可以优化溶液相条件以产生相对较低的电荷状态,从而减少电荷状态的模糊性和m/z重叠,但气相方法对电荷状态的降低提供了更大的控制。然而,对于复杂混合物,仅靠电荷状态降低往往无法解析混合物中的各个组分。在进行电荷状态操纵之前加入质量选择步骤可以简化混合物并显著改善组分的分离。这种一般的串联质谱方法在这里被称为通过离子z态操纵的前体分辨率(PRIZM)。PRIZM实验变体的例子可以追溯到大约25年前,涉及离子/分子质子转移反应、离子/离子质子转移反应、离子/离子电子转移反应、电子捕获反应和多电荷离子附着反应。本教程综述描述了PRIZM方法,并提供了使用上述每种电荷状态操纵方法的示例。

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本文引用的文献

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To 200,000 / and Beyond: Native Electron Capture Charge Reduction Mass Spectrometry Deconvolves Heterogeneous Signals in Large Biopharmaceutical Analytes.至200,000及以上:原生电子捕获电荷减少质谱法解析大型生物制药分析物中的异质信号。
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Surface Activity of Amines Provides Evidence for the Combined ESI Mechanism of Charge Reduction for Protein Complexes.胺的表面活性为蛋白质复合物的 ESI 电荷还原的联合机制提供了证据。
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Characterization of Homopolymer Distributions via Direct Infusion ESI-MS/MS using Wide Mass-to-Charge Windows and Gas-Phase Ion/Ion Reactions.通过使用宽质量电荷窗口和气相离子/离子反应的直接注入电喷雾质谱/质谱法对均聚物分布进行表征。
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