Development of a highly efficient solubilization method for mass spectrometric analysis of phospholipids in living single cells.

Detergent Lipidomics Phospholipid Single cell Single-cell mass spectrometry Trehalose C14 nanoESI

Journal

Analytical sciences : the international journal of the Japan Society for Analytical Chemistry
ISSN: 1348-2246
Titre abrégé: Anal Sci
Pays: Switzerland
ID NLM: 8511078

Informations de publication

Date de publication:
28 Mar 2024
Historique:
received: 11 12 2023
accepted: 20 02 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: aheadofprint

Résumé

Phospholipids are vital constituents of the cell membrane and aid in signal transduction. Phospholipid profiles vary distinctively with the cell type. Notably, specific phospholipid molecules are present in significantly higher or lower concentrations in cancer cells versus normal cells. In this study, live single-cell mass spectrometry (MS) was developed for analyzing phospholipids at the single-cell level. This method facilitates rapid molecular analysis of cells under microscopic observation. For nanoelectrospray ionization, phospholipids were extracted from single cells isolated in a glass capillary through a high-efficiency process. Cell-derived phosphatidylcholines were detected with high sensitivity when trehalose C14 was added as a solubilizing reagent. Trehalose C14 can solubilize cells at low concentrations owing to its low critical micelle concentration, and exerts minimal matrix effects (such as suppressing ionization and causing peak overlap) in the MS analysis of cellular molecules. Analyses of phospholipids in Raji and HEV0070 cells using the developed method revealed specific peaks of phosphatidylcholine and sphingomyelin in the respective cells. The developed technique not only affords phospholipid profiles at the single-cell level, but also holds promise for identifying biomarkers associated with various diseases, particularly cancer.

Identifiants

pubmed: 38546806
doi: 10.1007/s44211-024-00542-6
pii: 10.1007/s44211-024-00542-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Ministry of Education, Culture, Sports, Science and Technology
ID : 19K07028
Organisme : Ministry of Education, Culture, Sports, Science and Technology
ID : 22K06551

Informations de copyright

© 2024. The Author(s), under exclusive licence to The Japan Society for Analytical Chemistry.

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Auteurs

Jo Sakata (J)

School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-Ku, Shizuoka, Shizuoka, 422-8526, Japan.

Aogu Furusho (A)

School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-Ku, Shizuoka, Shizuoka, 422-8526, Japan.

Eiji Sugiyama (E)

School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-Ku, Shizuoka, Shizuoka, 422-8526, Japan.

Iwao Sakane (I)

Central Research Institute, ITO EN, Ltd., 21 Mekami, Makinohara, Shizuoka, 421-0516, Japan.

Kenichiro Todoroki (K)

School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-Ku, Shizuoka, Shizuoka, 422-8526, Japan.

Hajime Mizuno (H)

School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-Ku, Shizuoka, Shizuoka, 422-8526, Japan. hmizuno@meijo-u.ac.jp.
Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Tempaku-Ku, Nagoya, Aichi, 468-8503, Japan. hmizuno@meijo-u.ac.jp.

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