TY - JOUR
T1 - Improvement of Sensitivity and Reproducibility for Imaging of Endogenous Metabolites by Matrix-Assisted Laser Desorption/Ionization-Mass Spectrometry
AU - Morikawa-Ichinose, Tomomi
AU - Fujimura, Yoshinori
AU - Murayama, Fusa
AU - Yamazaki, Yuzo
AU - Yamamoto, Takushi
AU - Wariishi, Hiroyuki
AU - Miura, Daisuke
N1 - Funding Information:
This research was supported by the Science and Technology Incubation Program in Advanced Region from the funding program BCreation of Innovation Center for Advanced Interdisciplinary Research Areas^ from the Japan Science and Technology Agency, commissioned by the Ministry of Education, Culture, Sports, Science and Technology. This work was also supported in part by JSPS KAKENHI Grant Numbers 17H03819 (to Yoshinori Fujimura), 26713020 (to Daisuke Miura), and 15K14921 (to Daisuke Miura) and Grant-in-Aid for JSPS fellow 16J40073 (to Tomomi Morikawa-Ichinose).
Publisher Copyright:
© 2019, American Society for Mass Spectrometry.
PY - 2019/8/15
Y1 - 2019/8/15
N2 - Matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry imaging (MSI) is a powerful technique to visualize the distributions of biomolecules without any labeling. In MALDI-MSI experiments, the choice of matrix deposition method is important for acquiring favorable MSI data with high sensitivity and high reproducibility. Generally, manual or automated spray-coating and automated sublimation methods are used, but these methods have some drawbacks with respect to detection sensitivity, spatial resolution, and data reproducibility. Herein, we present an optimized matrix deposition method of sublimation coupled with recrystallization using 9-aminoacridine (9-AA) as a matrix capable of ionizing endogenous metabolites. The matrix recrystallization process after sublimation was optimized for the solvent concentration and reaction temperature for matrix–metabolite co-crystallization. This optimized method showed excellent reproducibility and spatial resolution compared to the automatic spray-coating method. Furthermore, the recrystallization step after sublimation remarkably improved the detectability of metabolites, including amino acids, nucleotide derivatives, and lipids, compared with the conventional sublimation method. To date, there have been no other reports of 9-AA-based sublimation combined with recrystallization. The present method provides an easy, sensitive, and reproducible matrix deposition method for MALDI-MSI of endogenous metabolites. [Figure not available: see fulltext.].
AB - Matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry imaging (MSI) is a powerful technique to visualize the distributions of biomolecules without any labeling. In MALDI-MSI experiments, the choice of matrix deposition method is important for acquiring favorable MSI data with high sensitivity and high reproducibility. Generally, manual or automated spray-coating and automated sublimation methods are used, but these methods have some drawbacks with respect to detection sensitivity, spatial resolution, and data reproducibility. Herein, we present an optimized matrix deposition method of sublimation coupled with recrystallization using 9-aminoacridine (9-AA) as a matrix capable of ionizing endogenous metabolites. The matrix recrystallization process after sublimation was optimized for the solvent concentration and reaction temperature for matrix–metabolite co-crystallization. This optimized method showed excellent reproducibility and spatial resolution compared to the automatic spray-coating method. Furthermore, the recrystallization step after sublimation remarkably improved the detectability of metabolites, including amino acids, nucleotide derivatives, and lipids, compared with the conventional sublimation method. To date, there have been no other reports of 9-AA-based sublimation combined with recrystallization. The present method provides an easy, sensitive, and reproducible matrix deposition method for MALDI-MSI of endogenous metabolites. [Figure not available: see fulltext.].
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U2 - 10.1007/s13361-019-02221-7
DO - 10.1007/s13361-019-02221-7
M3 - Article
C2 - 31044355
AN - SCOPUS:85065331220
SN - 1044-0305
VL - 30
SP - 1512
EP - 1520
JO - Journal of the American Society for Mass Spectrometry
JF - Journal of the American Society for Mass Spectrometry
IS - 8
ER -