Lin Xiangpeng, Pang Xuelei, Huang Yue, Duan Xinxin, Wei Yunfei, Jing Ning, Zhang Meng, Zhang Yu-Hui
MOE Key Laboratory for Biomedical Photonics, Advanced Biomedical Imaging Facility-Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, Hubei 430070, China.
ACS Cent Sci. 2025 Jul 29;11(9):1700-1714. doi: 10.1021/acscentsci.5c00695. eCollection 2025 Sep 24.
Delineating intricate mitochondrial dynamic changes over extended time scales through combined fluorescent probes and super-resolution microscopy is pivotal for deciphering the pathogenesis of mitochondrial-related diseases. However, a major challenge lies in the scarcity of probes that simultaneously exhibit robust labeling stability, exceptional photostability, and minimal cytotoxicity. Herein, rational design and screening yielded a novel covalent mitochondrial probe, HZ Mito Red. Due to its exceptional covalent labeling efficiency, HZ Mito Red exhibits superior mitochondrial labeling stability, with a 10-fold improvement compared to Mito Tracker Red (MTR). Furthermore, it exhibits remarkable photostability, retaining over 80% fluorescence after 300 SIM images, and negligible phototoxicity, preserving mitochondrial integrity even after 400 SIM images of continuous imaging. These advantageous properties facilitated the pioneering of high signal-to-noise, long-term dynamic SIM super-resolution imaging of mitochondria during ferroptosis, apoptosis, and autophagy, achieving unprecedented detailed delineation of mitochondrial morphology. Additionally, engineered for multichannel mitochondrial imaging, HZ Mito Deep Red mirrors the exceptional labeling stability of HZ Mito Red, achieving near-phototoxicity-free dynamic tracking with 60% fluorescence retention after 300 SIM images. Significantly, both HZ Mito Red and HZ Mito Deep Red are compatible with cell immunofluorescence staining. This study provides a robust and versatile tool for the in-depth analysis of mitochondrial dynamics in disease states.
通过组合荧光探针和超分辨率显微镜来描绘长时间尺度上复杂的线粒体动态变化,对于阐明线粒体相关疾病的发病机制至关重要。然而,一个主要挑战在于缺乏同时具有强大标记稳定性、出色光稳定性和最小细胞毒性的探针。在此,通过合理设计和筛选产生了一种新型共价线粒体探针HZ Mito Red。由于其出色的共价标记效率,HZ Mito Red表现出卓越的线粒体标记稳定性,与Mito Tracker Red(MTR)相比提高了10倍。此外,它具有显著的光稳定性,在300张结构光照明显微镜(SIM)图像后仍保留超过80%的荧光,并且光毒性可忽略不计,即使在连续成像400张SIM图像后仍能保持线粒体完整性。这些有利特性促进了在铁死亡、凋亡和自噬过程中线粒体的高信噪比、长期动态SIM超分辨率成像的开拓,实现了线粒体形态前所未有的详细描绘。此外,为多通道线粒体成像而设计的HZ Mito Deep Red反映了HZ Mito Red的出色标记稳定性,在300张SIM图像后实现了近无光照毒性的动态跟踪,荧光保留率为60%。重要的是,HZ Mito Red和HZ Mito Deep Red都与细胞免疫荧光染色兼容。这项研究为深入分析疾病状态下的线粒体动态提供了一种强大且通用的工具。