光漂白
线粒体内膜
活体细胞成像
生物物理学
扫描电镜
线粒体
化学
光漂白后的荧光恢复
共焦显微镜
显微镜
细胞生物学
共焦
细胞
膜
超分辨率
生物
荧光
生物化学
物理
光学
计算机科学
人工智能
图像(数学)
作者
Shuai Zheng,Neville Dadina,Deepto Mozumdar,Lauren Lesiak,Kayli Martinez,Evan W. Miller,Alanna Schepartz
标识
DOI:10.1038/s41589-023-01450-y
摘要
Abstract The inner mitochondrial membrane (IMM) generates power to drive cell function, and its dynamics control mitochondrial health and cellular homeostasis. Here, we describe the cell-permeant, lipid-like small molecule MAO-N 3 and use it to assemble high-density environmentally sensitive (HIDE) probes that selectively label and image the IMM in live cells and multiple cell states. MAO-N 3 pairs with strain-promoted azide–alkyne click chemistry-reactive fluorophores to support HIDE imaging using confocal, structured illumination, single-molecule localization and stimulated emission depletion microscopy, all with significantly improved resistance to photobleaching. These probes generate images with excellent spatial and temporal resolution, require no genetic manipulations, are non-toxic in model cell lines and primary cardiomyocytes (even under conditions that amplify the effects of mitochondrial toxins) and can visualize mitochondrial dynamics for 12.5 h. This probe will enable comprehensive studies of IMM dynamics with high temporal and spatial resolution.
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