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Visualization of Phospholipid Synthesis on Tissue Sections Using Functional Mass Spectrometry Imaging.
Iwama, Taiga; Kano, Kuniyuki; Kawana, Hiroki; Shindou, Hideo; Shimizu, Takao; Kono, Nozomu; Aoki, Junken.
Afiliação
  • Iwama T; Department of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.
  • Kano K; Department of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.
  • Kawana H; Department of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.
  • Shindou H; Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology. Nara 630-0192, Japan.
  • Shimizu T; Department of Lipid Life Science, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
  • Kono N; Department of Medical Lipid Science, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan.
  • Aoki J; Department of Lipid Signaling, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
Anal Chem ; 2024 Jul 12.
Article em En | MEDLINE | ID: mdl-38995673
ABSTRACT
Functional mass spectrometry imaging (fMSI) is a potent tool for elucidating the spatial distribution of enzyme activities in tissues at high resolution. In this study, we applied fMSI to probe the intricate biosynthesis of phospholipids, which exist as thousands of molecular species in tissues and exhibit a unique distribution specific to cell type. By using deuterium- and 13C-labeled substrates, we visualized the activities of key enzymes involved in phospholipid synthesis, including glycerol 3-phosphate acyltransferase (GPAT), lysophosphatidic acid acyltransferases (LPAAT), lysophospholipid acyltransferases (LPLAT), and long-chain acyl-CoA synthetase (ACSL). Additionally, we were able to visualize a two-step sequential enzyme reaction involving ACSL and LPLAT. This novel approach unveiled significant variations in enzyme activity distribution depending on the type of fatty acids used as substrates. It will also help to reveal the mechanisms underlying the formation of numerous phospholipid species.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Anal Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Anal Chem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão
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