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一种基于聚集/单体的探针,用于监测铜死亡过程中线粒体-溶酶体的相互作用。

An Aggregation/Monomer-Based Probe for Monitoring Mitochondria-Lysosome Interactions during Cuproptosis.

作者信息

Zhou Cui, Yan Jia-Tong, Chu Yi-Ting, Wang Jian, Tang Gui-Xue, Chen Shuo-Bin, Huang Zhi-Shu, Tan Jia-Heng, Chen Xiu-Cai

机构信息

Guangdong Provincial Key Laboratory of New Drug Design and Evaluation, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.

School of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou, 510006, China.

出版信息

Anal Chem. 2025 Jul 1;97(25):13168-13175. doi: 10.1021/acs.analchem.5c00971. Epub 2025 Jun 20.

Abstract

The interplay between lysosomes and mitochondria is essential for maintaining cellular function, and disruptions of their interaction have been implicated in the onset of various diseases. Small molecule fluorescent probes are powerful tools for monitoring these biological processes. However, a comprehensive strategy for designing small-molecule probes capable of dual-color visualization of both mitochondria and lysosomes remains lacking. In this study, we introduce , a noninvasive small organic molecular probe, as an effective tool for tracking the dynamic interplay between mitochondria and lysosomes in living cells. Mechanistic studies revealed that targets lysosomes in a monomeric state, exhibiting green fluorescence, and in an aggregated state within mitochondria, displaying red fluorescence. Using , we were able to perform long-term tracking of dynamic mitochondria-lysosome interactions and identified several distinct types of interactions between these organelles. Notably, for the first time, revealed changes in mitochondria-lysosome interactions during cuproptosis, suggesting that the modulation of these interactions may influence this form of cell death. This work presents a valuable tool for real-time monitoring of functional mitochondria-lysosome interactions in living cells and opens avenues for advancing our understanding of related cellular processes and disease mechanisms.

摘要

溶酶体与线粒体之间的相互作用对于维持细胞功能至关重要,它们相互作用的破坏与多种疾病的发生有关。小分子荧光探针是监测这些生物过程的有力工具。然而,目前仍缺乏一种能够对线粒体和溶酶体进行双色可视化的小分子探针设计综合策略。在本研究中,我们引入了一种非侵入性的小分子有机分子探针,作为追踪活细胞中线粒体与溶酶体动态相互作用的有效工具。机理研究表明,该探针以单体状态靶向溶酶体,发出绿色荧光,而在线粒体内以聚集状态存在时,发出红色荧光。利用该探针,我们能够对线粒体 - 溶酶体的动态相互作用进行长期追踪,并确定了这些细胞器之间几种不同类型的相互作用。值得注意的是,该探针首次揭示了铜死亡过程中线粒体 - 溶酶体相互作用的变化,表明对这些相互作用的调节可能影响这种细胞死亡形式。这项工作为实时监测活细胞中功能性线粒体 - 溶酶体相互作用提供了一个有价值的工具,并为增进我们对相关细胞过程和疾病机制的理解开辟了道路。

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