用基质辅助激光解吸/电离质谱法对5-硝基水杨酸和1,5-二氨基萘进行腺嘌呤、鸟嘌呤和黄嘌呤衍生物的结构分类

IF 3.1 2区 化学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of the American Society for Mass Spectrometry Pub Date : 2025-01-04 DOI:10.1021/jasms.4c00405
Tohru Yamagaki, Mika Nobuhara
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引用次数: 0

摘要

本研究以α-氰基-4-羟基肉桂酸(CHCA)、1,5-二氨基萘(DAN)、5-甲酰水杨酸(FSA)和5-硝基水杨酸(NSA)为基质,采用多基质变异基质辅助激光解吸电离质谱法(MALDI MS)分析嘌呤衍生物。此外,我们重点研究了从分析物中提取/附着氢,并在含有氮和/或羰基氧的化合物的MALDI质谱中检测到[M - H]+, [M + 2H]+•和/或[M + 3H]+。虽然用传统基质在MALDI质谱中生成[M - H]+嘌呤化合物具有挑战性,但与CHCA、FSA和DAN相比,NSA-MALDI质谱有效地生成了[M - H]+类嘌呤衍生物,且[M - H]+/[M + H]+比值反映了嘌呤衍生物的结构,如取代基和位置。我们推测,在胺基α-碳上通过NSA基质生成了分子离子[M]+•并进行了随后的氢自由基提取。在光化学反应中,NSA的硝基(-NO2)具有清除氢自由基的作用。腺苷、鸟苷和肌苷的[M - H]+表明氢的提取发生在核糖单元。利用NSA-MALDI质谱法将副黄嘌呤的黄嘌呤同分异构体与茶碱和可可碱的黄嘌呤同分异构体的[M - H]+/[M + H]+比值进行了区分。此外,由于黄嘌呤衍生物的羰基,在DAN-MALDI质谱法中生成了[M + 2H]+•。黄嘌呤衍生物的[M + 2H]+•的相对丰度远高于其他嘌呤衍生物,如腺嘌呤衍生物在其DAN- maldi ms中生成[M + 3H]+, DAN诱导嘌呤化合物的氢附着是因为DAN的胺基(-NH2)在光化学反应中可以产生氢自由基。NSA-和DAN-MALDI质谱对嘌呤衍生物进行了表征,并对其结构进行了分类。
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Structural Categorization of Adenine, Guanine, and Xanthine Derivatives Using Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry with 5-Nitrosalicylic Acid and 1,5-Diaminonaphtalene.

In this study, we analyzed purine derivatives using multimatrix variation matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) with α-cyano-4-hydroxycinnamic acid (CHCA), 1,5-diaminonaphtalene (DAN), 5-formylsalicylic acid (FSA), and 5-nitrosalicylic acid (NSA) as matrices. Further, we focused on the abstraction/attachment of hydrogen from/to analytes and detected [M - H]+, [M + 2H]+• and/or [M + 3H]+ in MALDI MS spectra of compounds containing nitrogen and/or carbonyl oxygen. Although [M - H]+ generation of purine compounds in MALDI MS with conventional matrices was challenging, NSA-MALDI MS effectively yielded the [M - H]+species of purine derivatives compared with CHCA, FSA, and DAN, and the [M - H]+/[M + H]+ ratios reflected their structures, such as the substituting groups and positions. We speculated that the molecular ion [M]+• generated and the subsequent hydrogen radical abstraction proceeded by NSA matrix from the α-carbon of the amine group. The nitro group (-NO2) of NSA can withdraw hydrogen radicals in photochemical reactions. The [M - H]+ of adenosine, guanosine, and inosine suggested that hydrogen abstraction occurred in the ribose unit. The xanthine isomer of paraxanthine was distinguished from those of theophylline and theobromine using their [M - H]+/[M + H]+ ratios obtained with NSA-MALDI MS. Additionally, [M + 2H]+• generated in DAN-MALDI MS of xanthine derivatives due to their carbonyl groups. The relative abundances of [M + 2H]+• of xanthine derivatives were much higher than those of the other purine derivatives such as adenine derivatives which generated [M + 3H]+ in their DAN-MALDI MS. DAN induced the hydrogen attachment of purine compounds because the amine group (-NH2) of DAN can give hydrogen radicals in photochemical reactions. NSA- and DAN-MALDI MS characterized purine derivatives and were useful for their structure categorization.

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来源期刊
CiteScore
5.50
自引率
9.40%
发文量
257
审稿时长
1 months
期刊介绍: The Journal of the American Society for Mass Spectrometry presents research papers covering all aspects of mass spectrometry, incorporating coverage of fields of scientific inquiry in which mass spectrometry can play a role. Comprehensive in scope, the journal publishes papers on both fundamentals and applications of mass spectrometry. Fundamental subjects include instrumentation principles, design, and demonstration, structures and chemical properties of gas-phase ions, studies of thermodynamic properties, ion spectroscopy, chemical kinetics, mechanisms of ionization, theories of ion fragmentation, cluster ions, and potential energy surfaces. In addition to full papers, the journal offers Communications, Application Notes, and Accounts and Perspectives
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