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Furao Li, Chunyan Liang, Xifeng Mo, Xiaohuan Xu, Yongbiao Wei, Chunyan Zhou, Ting Meng, Hui Zhang, Fan Yang. Cuproptosis tracker: Visualizing organelle dynamics with a dual-targeted fluorescent probe[J]. Journal of Pharmaceutical Analysis. doi: 10.1016/j.jpha.2025.101500
Citation: Furao Li, Chunyan Liang, Xifeng Mo, Xiaohuan Xu, Yongbiao Wei, Chunyan Zhou, Ting Meng, Hui Zhang, Fan Yang. Cuproptosis tracker: Visualizing organelle dynamics with a dual-targeted fluorescent probe[J]. Journal of Pharmaceutical Analysis. doi: 10.1016/j.jpha.2025.101500

Cuproptosis tracker: Visualizing organelle dynamics with a dual-targeted fluorescent probe

doi: 10.1016/j.jpha.2025.101500
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This work was supported by the Natural Science Foundation of Guangxi (Grant Nos.: AD23026319, 2021GXNSFFA220003 and 2022GXNSFDA035072), the Guangxi Science and Technology Major Program (Grant No: AA24011005), the National Natural Science Foundation of China (Grant Nos: 22468016 and 22264007), First-class discipline innovation-driven talent program of Guangxi Medical University, Guangxi Major Talent Program, and Guangxi Medical University Training Program for Distinguished Young Scholars.

  • Received Date: May 13, 2025
  • Accepted Date: Nov. 27, 2025
  • Rev Recd Date: Nov. 24, 2025
  • Available Online: Nov. 29, 2025
  • Cuproptosis often interacts with mitochondrial (Mito) dysfunction and lipid droplets (LDs) metabolism disturbances, thus resulting in programmed cell death, whereas their dynamic interaction lacks a rational analyzing tool. Herein, we show a Mito-LDs dual-targeted fluorescent reporter (MLR) for tracking the Mito-LDs interaction during cuproptosis by dynamic monitoring of intracellular sulfur dioxide (SO2) dynamics. MLR integrates a coumarin-derived SO2-responsive core linked via piperazine to a benzopyronium Mitol anchor, enabling one-step synthesis with exceptional sensitivity (0.34 μM) and rapid response (<10 s). Live-cell imaging demonstrated MLR’s SO2-triggered translocation from Mito to LDs during cuproptosis, directly visualizing inter-organelle communication. Dual fluorescence channel imaging associated SO2 fluctuations with Mito-LDs targeting, revealing the interaction between LDs-Mito during Cu2+ and elesclomol induced apoptosis. In addition to imaging, MLR-based test strips and hydrogels can achieve rapid (< 1 min) on-site SO2 detection. As a dual-organelle tracer for cuproptosis, MLR overcomes single-target probe limitations, offering a transformative platform to analyze spatiotemporal organelle dynamics for advancing diagnostic tools development.
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