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单个线粒体的阴影电化学发光显微镜观察

Shadow Electrochemiluminescence Microscopy of Single Mitochondria.

机构信息

University of Bordeaux, Bordeaux INP, ISM, UMR CNRS 5255, 33607, Pessac, France.

Present address: Univ. Bordeaux, CNRS, Bordeaux INP, CBMN UMR 5248, Allée Geoffroy Saint Hilaire, 33600, Pessac, France.

出版信息

Angew Chem Int Ed Engl. 2021 Aug 16;60(34):18742-18749. doi: 10.1002/anie.202105867. Epub 2021 Jul 16.

Abstract

Mitochondria are the subcellular bioenergetic organelles. The analysis of their morphology and topology is essential to provide useful information on their activity and metabolism. Herein, we report a label-free shadow electrochemiluminescence (ECL) microscopy based on the spatial confinement of the ECL-emitting reactive layer to image single living mitochondria deposited on the electrode surface. The ECL mechanism of the freely-diffusing [Ru(bpy) ] dye with the sacrificial tri-n-propylamine coreactant restrains the light-emitting region to a micrometric thickness allowing to visualize individual mitochondria with a remarkable sharp negative optical contrast. The imaging approach named "shadow ECL" (SECL) reflects the negative imprint of the local diffusional hindrance of the ECL reagents by each mitochondrion. The statistical analysis of the colocalization of the shadow ECL spots with the functional mitochondria revealed by classical fluorescent biomarkers, MitoTracker Deep Red and the endogenous intramitochondrial NADH, validates the reported methodology. The versatility and extreme sensitivity of the approach are further demonstrated by visualizing single mitochondria, which remain hardly detectable with the usual biomarkers. Finally, by alleviating problems of photobleaching and phototoxicity associated with conventional microscopy methods, SECL microscopy should find promising applications in the imaging of subcellular structures.

摘要

线粒体是细胞内的生物能量细胞器。分析其形态和拓扑结构对于提供有关其活性和代谢的有用信息至关重要。在此,我们报告了一种无标记的阴影电化学发光(ECL)显微镜,该显微镜基于 ECL 发光反应层的空间限制,可对沉积在电极表面上的单个活线粒体进行成像。带有牺牲三丙胺共反应物的自由扩散[Ru(bpy)]染料的 ECL 机制将发光区域限制在微米厚度内,从而可以用显著的负光学对比度对单个线粒体进行可视化。这种成像方法称为“阴影 ECL”(SECL),反映了 ECL 试剂通过每个线粒体的局部扩散阻碍的负印记。通过与经典荧光生物标志物(MitoTracker Deep Red 和内源性线粒体 NADH)进行功能线粒体的共定位的统计分析,验证了所报道的方法。该方法的多功能性和极高的灵敏度通过可视化单个线粒体得到了进一步证明,而通常的生物标志物几乎无法检测到这些线粒体。最后,通过缓解与传统显微镜方法相关的光漂白和光毒性问题,SECL 显微镜应该在亚细胞结构成像中找到有前途的应用。

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