Neta Pedatsur, Farahani Mahnaz, Simón-Manso Yamil, Liang Yuxue, Yang Xiaoyu, Stein Stephen E
Biomolecular Measurement Division, National Institute of Standards and Technology, Gaithersburg, MD, 20899, USA.
Rapid Commun Mass Spectrom. 2014 Dec 15;28(23):2645-60. doi: 10.1002/rcm.7055.
Certain product ions in electrospray ionization tandem mass spectrometry are found to react with residual water in the collision cell. This reaction often leads to the formation of ions that cannot be formed directly from the precursor ions, and this complicates the mass spectra and may distort MRM (multiple reaction monitoring) results.
Various drugs, pesticides, metabolites, and other compounds were dissolved in acetonitrile/water/formic acid and studied by electrospray ionization mass spectrometry to record their MS(2) and MS(n) spectra in several mass spectrometers (QqQ, QTOF, IT, and Orbitrap HCD). Certain product ions were found to react with residual water in collision cells. The reaction was confirmed by MS(n) studies and the rate of reaction was determined in the IT instrument using zero collision energy and variable activation times.
Examples of product ions reacting with water include phenyl and certain substituted phenyl cations, benzoyl-type cations formed from protonated folic acid and similar compounds by loss of the glutamate moiety, product ions formed from protonated cyclic siloxanes by loss of methane, product ions formed from organic phosphates, and certain negative ions. The reactions of product ions with residual water varied greatly in their rate constant and in the extent of reaction (due to isomerization).
Various types of product ions react with residual water in mass spectrometer collision cells. As a result, tandem mass spectra may contain unexplained peaks and MRM results may be distorted by the occurrence of such reactions. These often unavoidable reactions must be taken into account when annotating peaks in tandem mass spectra and when interpreting MRM results. Published in 2014. This article is a U.S. Government work and is in the public domain in the USA.
在电喷雾电离串联质谱中,发现某些产物离子会与碰撞池中残留的水发生反应。这种反应常常导致形成无法直接从前体离子形成的离子,这会使质谱图变得复杂,并可能扭曲多反应监测(MRM)结果。
将各种药物、农药、代谢物及其他化合物溶解于乙腈/水/甲酸中,通过电喷雾电离质谱进行研究,以记录它们在几种质谱仪(三重四极杆质谱仪、飞行时间质谱仪、离子阱质谱仪和轨道阱高分辨碰撞诱导解离质谱仪)中的二级质谱(MS(2))和多级质谱(MS(n))谱图。发现某些产物离子会与碰撞池中的残留水发生反应。通过多级质谱研究证实了该反应,并在离子阱质谱仪中使用零碰撞能量和可变激活时间确定了反应速率。
与水发生反应的产物离子示例包括苯基及某些取代苯基阳离子、由质子化叶酸及类似化合物失去谷氨酸部分形成的苯甲酰型阳离子、由质子化环硅氧烷失去甲烷形成的产物离子、由有机磷酸盐形成的产物离子以及某些负离子。产物离子与残留水的反应在速率常数和反应程度(由于异构化)方面差异很大。
各类产物离子会与质谱仪碰撞池中的残留水发生反应。因此,串联质谱图可能包含无法解释的峰,并且此类反应的发生可能会扭曲多反应监测结果。在注释串联质谱图中的峰以及解释多反应监测结果时,必须考虑这些通常不可避免的反应。于2014年发表。本文为美国政府作品,在美国属于公共领域。