Using HBmito Crimson to Observe Mitochondrial Cristae Through STED Microscopy

Authors:

Xichuan Ge, Wei Ren, Chunyan Shan, Peng Xi, Baoxiang Gao

Keywords:

Live cell imaging; Super-resolution imaging; Mitochondria cristae; Low-saturation power; Fluorescence labeling

Abstract:

Mitochondrial cristae, formed by folding the mitochondrial inner membrane (IM), are essential for cellular energy supply. However, the observation of the IM is challenging due to the limitations in spatiotemporal resolution offered by conventional microscopy and the absence of suitable in vitro probes speciﬁcally targeting the IM. Here, we describe a detailed imaging protocol for the mitochondrial inner membrane using the Si-rhodamine dye HBmito Crimson, which has excellent photophysical properties, to label live cells for imaging via stimulated emission depletion (STED) microscopy. This allows for STED imaging over more than 500 frames (approximately one hour), with a spatial resolution of 40 nm, enabling the observation of cristae dynamics during various mitochondrial processes. The protocol includes detailed steps for cell staining, image acquisition, image processing, and resolution analysis. Utilizing the superior resolution of STED microscopy, the structure and complex dynamic changes of cristae can be visualized.

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