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Live-Cell Imaging Analysis of the Intracellular Behavior of the C-Type Lectin Receptor Mincle and Its Ligand Using Newly Developed Fluorescence-Labeled Molecular Probes Based on Trehalose Diester
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Live-Cell Imaging Analysis of the Intracellular Behavior of the C-Type Lectin Receptor Mincle and Its Ligand Using Newly Developed Fluorescence-Labeled Molecular Probes Based on Trehalose Diester

Takanori Matsumaru, Kana Okubo, Juri Takayama, Yuki Hirano, Yi-Ren Huo, Satomi Toguchi, Kenji Yoshida, Ayumi Fujii, Takehiro Suzuki, Chun-Cheng Lin, …
ACS chemical biology, 卷.21(3), 頁碼.519-526
20/03/2026
PMID: 41693385
Web of Science ID: WOS:001691786500001

摘要

Animals Cord Factors - chemistry Fluorescent Chemosensor Compounds Fluorescent Dyes - chemistry Humans Lectins, C-Type - analysis Lectins, C-Type - metabolism Ligands Membrane Proteins Receptors, Immunologic Trehalose - chemistry Trehalose - metabolism
Mincle, a member of the C-type lectin receptor (CLR) family, detects various glycolipids and glycerolipids such as trehalose dimycolate (TDM) from , leading to the activation of the innate immune system. In this study, we developed new fluorescence-labeled molecular probes, TDE-Fluor-Ligand and TDE-Reactive-Probe, based on the structure of trehalose diester to elucidate the intracellular behavior of Mincle and its ligands. TDE-Fluor-Ligand was prepared for the ligand analysis, and TDE-Reactive-Probe was specifically designed to label Mincle by turn-on fluorescent affinity labeling. Live-cell imaging analysis using these probes revealed that TDE-Fluor-Ligand internalizes into the cell in a Mincle-dependent manner. Furthermore, imaging analysis using TDE-Reactive-Probe successfully detected Mincle in cells in a Mincle expression-dependent manner.

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