Highly photostable fluorescent probes for multi-color and super-resolution imaging of cell organelles

被引:11
作者
Byun, Gyuwon [1 ]
Kim, Soh-Youn [2 ,3 ]
Choi, Min-Woo [1 ]
Yang, Jin-Kyoung [2 ]
Kwon, Ji Eon [4 ]
Kim, Sehoon [2 ,3 ]
Park, Soo Young [1 ]
机构
[1] Seoul Natl Univ, Dept Mat Sci & Engn, Seoul 151744, South Korea
[2] Korea Inst Sci & Technol, Ctr Theragnosis, Hwarang Ro 14 Gil 5, Seoul 136791, South Korea
[3] Korea Univ, KU KIST Grad Sch Converging Sci & Technol, Anam Ro 145, Seoul 02841, South Korea
[4] Korea Inst Sci & Technol KIST, Funct Composite Mat Res Ctr, Jeonbuk 55324, South Korea
关键词
Photostability; Fluorescent probe; Cell organelle imaging; Multi-color imaging; Super-resolution imaging; FLUOROPHORES; EMISSION; LYSOSOME;
D O I
10.1016/j.dyepig.2022.110427
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
High-performance microscopy with organelle-targeting fluorescent probes has been an indispensable bioimaging tool for cell biology. Confocal or super-resolution imaging often requires highly magnified and/or longitudinal scanning conditions, necessitating the advent of photostable fluorophores. Herein, we report novel organelle targeting fluorescent probes derived from a highly photostable fluorophoric skeleton, i.e., 1,5-naphthyridine2,6-dione (NTD). With organelle-specific derivatization and pi-conjugation extention, we developed NTD-based molecular probes with blue-to-red fluorescence tunability and intracellular organelle selectivity for staining, as well as minimal cytotoxicity, which allowed us to demonstrate intracellular differentiation of lysosomes and mitochondria by multi-color confocal imaging. Under the condition of longitudinal microscopic examination, these new probes showed excellent photostability of fluorescent signals as opposed to the rapid photobleaching of commercial trackers. By virtue of these beneficial properties, the NTD-based probes were successfully applied to super-resolution cell imaging by enduring the high-power illumination conditions of sub-diffraction microscopic techniques including stimulated emission depletion (STED) and structured illumination microscopy (SIM).
引用
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页数:9
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