Fluorescent Polymer Dot-Based Multicolor Stimulated Emission Depletion Nanoscopy with a Single Laser Beam Pair for Cellular Tracking

• Published in: Analytical chemistry (Washington) 2020-09, Vol.92 (17), p.12088-12096
• Main Authors: Wu, Yayun, Ruan, Hefei, Dong, Zaizai, Zhao, Rong, Yu, Jianqiang, Tang, Xiaojun, Kou, Xiaolong, Zhang, Xing, Wu, Manchen, Luo, Fang, Yuan, Jinghe, Fang, Xiaohong
• Format: Article
• Language: English
• Subjects: Caveolae; Cell Tracking - methods; Chemistry; Clathrin; Color; Confocal microscopy; Crosstalk; Depletion; Emission; Emissions; Endosomes; Fluorene; Fluorescence; Fluorescent Dyes - therapeutic use; Fluorescent indicators; Humans; Interaction models; Laser beams; Lasers; Medical imaging; Microscopy; Organelles; Photobleaching; Polymers; Polymers - chemistry; Probes; Quantum Dots - chemistry; Stimulated emission; Tracking; Wavelengths
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.0c02821

Stimulated emission depletion (STED) nanoscopy provides subdiffraction resolution while preserving the benefits of fluorescence confocal microscopy in live-cell imaging. However, there are several challenges for multicolor STED nanoscopy, including sophisticated microscopy architectures, fast photobleaching, and cross talk of fluorescent probes. Here, we introduce two types of nanoscale fluorescent semiconducting polymer dots (Pdots) with different emission wavelengths: CNPPV (poly­[2-methoxy-5-(2-ethylhexyloxy)-1,4-(1-cyanovinylene-1,4-phenylene)]) Pdots and PDFDP (poly­[{9,9-dihexyl-2,7-bis­(1-cyanovinylene)­fluorene}-alt-co-{2,5-bis (N,N′-diphenylamino)-1,4-phenylene}]) Pdots, for dual-color STED bioimaging and cellular tracking. Besides bright fluorescence, strong photostability, and easy bioconjugation, these Pdots have large Stokes shifts, which make it possible to share both excitation and depletion beams, thus requiring only a single pair of laser beams for the dual-color STED imaging. Long-term tracking of cellular organelles by the Pdots has been achieved in living cells, and the dynamic interaction of endosomes derived from clathrin-mediated and caveolae-mediated endocytic pathways has been monitored for the first time to propose their interaction models. These results demonstrate the promise of Pdots as excellent probes for live-cell multicolor STED nanoscopy.