{"title":"Influence of acceleration field and inlet temperature on ion yields of small molecules in atmospheric pressure MALDI","authors":"Eugene Moskovets","doi":"10.1016/j.ijms.2025.117535","DOIUrl":null,"url":null,"abstract":"<div><div>The optimization of the accelerating electric field near a target plate as well as temperature of the inlet capillary in a mass spectrometer is essential for achieving a high ion yield in atmospheric pressure matrix-assisted laser desorption ionization (AP/MALDI) and atmospheric pressure/laser desorption ionization (AP/LDI). The yields of protonated rhodamine 6G ions, protonated matrix ions (M + H)<sup>+</sup>, matrix radical ions (M•)<sup>+</sup>, as well as protonated reserpine ions were studied as a function of the inlet capillary temperature in Orbitrap and electric field applied across the inlet and MALDI target plate. The findings indicated that 2,5-dihydroxybenzoic acid (DHB) generated predominantly cation radicals (M•)<sup>+</sup> rather than protonated ions. This trend is not common for most MALDI matrices used for positive-mode MALDI-MS analysis. By changing capillary temperature, it has been found that the temperature trends observed for the (DHB + H)<sup>+</sup>/(DHB•)<sup>+</sup> ratios in both AP/MALDI and electrospray ionization (ESI) are similar. The ion yield dependence on the electric field strength in AP/MALDI as well as low-pressure MALDI sources proved to be more complex than that suggested in the previously developed model accounting for charge neutralization in the plume mitigated by the field-driven separation of opposite charges. The laser photoionization of the matrix molecules within a thin surface layer of a matrix microcrystal followed by thermally activated proton transfer from the matrix radical cation to adjacent matrix molecules has been discussed.</div></div>","PeriodicalId":338,"journal":{"name":"International Journal of Mass Spectrometry","volume":"519 ","pages":"Article 117535"},"PeriodicalIF":1.7000,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Mass Spectrometry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1387380625001393","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHYSICS, ATOMIC, MOLECULAR & CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The optimization of the accelerating electric field near a target plate as well as temperature of the inlet capillary in a mass spectrometer is essential for achieving a high ion yield in atmospheric pressure matrix-assisted laser desorption ionization (AP/MALDI) and atmospheric pressure/laser desorption ionization (AP/LDI). The yields of protonated rhodamine 6G ions, protonated matrix ions (M + H)+, matrix radical ions (M•)+, as well as protonated reserpine ions were studied as a function of the inlet capillary temperature in Orbitrap and electric field applied across the inlet and MALDI target plate. The findings indicated that 2,5-dihydroxybenzoic acid (DHB) generated predominantly cation radicals (M•)+ rather than protonated ions. This trend is not common for most MALDI matrices used for positive-mode MALDI-MS analysis. By changing capillary temperature, it has been found that the temperature trends observed for the (DHB + H)+/(DHB•)+ ratios in both AP/MALDI and electrospray ionization (ESI) are similar. The ion yield dependence on the electric field strength in AP/MALDI as well as low-pressure MALDI sources proved to be more complex than that suggested in the previously developed model accounting for charge neutralization in the plume mitigated by the field-driven separation of opposite charges. The laser photoionization of the matrix molecules within a thin surface layer of a matrix microcrystal followed by thermally activated proton transfer from the matrix radical cation to adjacent matrix molecules has been discussed.
期刊介绍:
The journal invites papers that advance the field of mass spectrometry by exploring fundamental aspects of ion processes using both the experimental and theoretical approaches, developing new instrumentation and experimental strategies for chemical analysis using mass spectrometry, developing new computational strategies for data interpretation and integration, reporting new applications of mass spectrometry and hyphenated techniques in biology, chemistry, geology, and physics.
Papers, in which standard mass spectrometry techniques are used for analysis will not be considered.
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