Dynamic tracking of the spatiotemporal coordination among various organelles to in-depth understanding of the mechanism of autophagy have attracted considerable attentions. However, the monitor of nucleoli participation in autophagy was… Click to show full abstract
Dynamic tracking of the spatiotemporal coordination among various organelles to in-depth understanding of the mechanism of autophagy have attracted considerable attentions. However, the monitor of nucleoli participation in autophagy was somehow neglected. Herein, we report a RNA-targeted bio-probe (ADAP) with high selective permeability into nuclear pore complexes, which induced two-photon (TP) fluorescence "off-on" response by groove combination with RNA, dynamically monitoring the autophagy process among multi-organelles (nucleoli, mitochondria and mitochondria-containing lysosomes). This work provides a simple and convenient way to observe the dynamic behavior of multi-organelles during the autophagy process, which benefits for the understanding of cellular metabolism.
               
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