Guangxi Key Laboratory of Pharmaceutical Precision Detection and Screening, Key Laboratory of Micro-Nanoscale Bioanalysis and Drug Screening of Guangxi Education Department, Pharmaceutical College, State Key Laboratory of Targeting Oncology, Guangxi Medical University, Nanning 530021, China
Funds:
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.
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.