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Shan, C.

Publications and source records attributed to Shan, C..

2 recordsLinked to original sources

Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe

Mitochondria play a critical role in generating energy to support the entire lifecycle of biological cells, yet it is still unclear how their morphological structures evolve to regulate their functionality. Conventional fluorescence microscopy can only provide [~]300 nm resolution, which is insufficient to visualize mitochondrial cristae. Here, we developed an enhanced squaraine variant dye (MitoESq-635) to study the dynamic structures of mitochondrial cristae in live cells at superresolution. The low saturation intensity and high photostability make it ideal for long-term, high-resolution STED nanoscopy. We demonstrate the time-lapsed imaging of the mitochondrial inner membrane over 50 minutes in living HeLa cells at 35.2 nm resolution for the first time. The forms of the cristae during mitochondrial fusion and fission can be clearly resolved. Our study demonstrates the emerging capability of optical STED nanoscopy to investigate intracellular physiological processes at nanoscale resolution for long periods of time with minimal phototoxicity.

biophysics

Fast, Accurate Polarization and Polarity Imaging withPolarized Structured Illumination

The orientation and wobbling behavior of the fluorescent dipoles are of great significance in revealing the structure and state of cells. Due to the poor optical sectioning capability of wide-field microscopy, the polarization modulation signals are susceptible to the neighboring fluorophores. The missing cone of wide field optical transfer function induces vast out-of-focus background, resulting in biased polarization orientation and decrease polarization factor. Here, we apply polarized structured illumination to achieve polarization modulation imaging with optical sectioning, and simultaneously measure the lipid polarity with two-color ratiometric imaging. Our results demonstrate a significant increase in measurement accuracy of not only the dipole orientations but also the wobbling behavior of the ensemble dipole. Compared to the conventional confocal polarization imaging, our method obtains an order-of-magnitude faster imaging speed, capturing the fast dynamics of subcellular structures in live cells.

biophysics