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Enhanced specificity for phosphatidylcholine analysis by positive ion mode matrix‐assisted laser desorption/ionization imaging mass spectrometry
Author(s) -
Zaima Nobuhiro,
Yoshioka Sayaka,
Sato Yayoi,
Shinano Saki,
Ikeda Yoshihiko,
Moriyama Tatsuya
Publication year - 2014
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.6917
Subject(s) - chemistry , mass spectrometry imaging , ammonium acetate , mass spectrometry , desorption , matrix assisted laser desorption/ionization , potassium , chromatography , phosphatidylcholine , matrix (chemical analysis) , maldi imaging , quantitative analysis (chemistry) , analytical chemistry (journal) , ion , high performance liquid chromatography , biochemistry , phospholipid , organic chemistry , adsorption , membrane
RATIONALE Visualization of the spatial distribution of phosphatidylcholine (PC) in tissues by matrix‐assisted laser desorption/ionization imaging mass spectrometry (MALDI‐IMS) provides insights into key physiological and pathophysiological processes. In MALDI‐IMS analysis, the heterogeneity of adduct ions formed from PC lowers the specificity of detection of PC molecular species and poses a challenge in the identification of these species. To solve this problem, modified matrix solution and desalting with ammonium acetate (NH 4 Ac) buffer have been employed. However, the utility of these methods is limited to the analysis of brain sections. METHODS The MALDI signal intensities of [PC+H], [PC+Na] and [PC+K] were compared after three different pretreatments (modified matrix solution, desalting with 150 mM ammonium acetate, treatment with 150 mM potassium acetate). RESULTS Pretreatment of tissue sections with 150 mM potassium acetate resulted in an increase in the signal intensity of [PC+K] ions produced from cryosections of the pancreas, brain, and liver tissues. CONCLUSIONS Pretreatment with potassium acetate can be a simple, improved, and highly useful method for the reliable analysis of PC in tissues. Copyright © 2014 John Wiley & Sons, Ltd.

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