Gas-Phase Stability of Negatively Charged Organophosphate Metabolites Produced by Electrospray Ionization and Matrix-Assisted Laser Desorption/Ionization

被引:10
作者
Asakawa, Daiki [1 ]
Mizuno, Hajime [2 ]
Toyo'oka, Toshimasa [2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Tsukuba Cent 2,Umezono 1-1-1, Tsukuba, Ibaraki 3058568, Japan
[2] Univ Shizuoka, Sch Pharmaceut Sci, Lab Analyt & Bioanalyt Chem, Suruga Ku, 52-1 Yada, Shizuoka 4228526, Japan
关键词
Charge state; Fragmentation; ADP; ATP; Density functional theory; MASS-SPECTROMETRY; INTERNAL ENERGY; PROTEINS; SOLVENT; ANIONS; STABILIZATION; DISTRIBUTIONS; BIOMOLECULES; STATES;
D O I
10.1007/s13361-017-1795-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The formation mechanisms of singly and multiply charged organophosphate metabolites by electrospray ionization (ESI) and their gas phase stabilities were investigated. Metabolites containing multiple phosphate groups, such as adenosine 5'-diphosphate (ADP), adenosine 5'-triphosphate (ATP), and D-myo-inositol-1,4,5-triphosphate (IP3) were observed as doubly deprotonated ions by negative-ion ESI mass spectrometry. Organophosphates with multiple negative charges were found to be unstable and often underwent loss of PO3 (-), although singly deprotonated analytes were stable. The presence of fragments due to the loss of PO3 (-) in the negative-ion ESI mass spectra could result in the misinterpretation of analytical results. In contrast to ESI, matrix-assisted laser desorption ionization (MALDI) produced singly charged organophosphate metabolites with no associated fragmentation, since the singly charged anions are stable. The stability of an organophosphate metabolite in the gas phase strongly depends on its charge state. The fragmentations of multiply charged organophosphates were also investigated in detail through density functional theory calculations.
引用
收藏
页码:2561 / 2568
页数:8
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