Gentle Rhodamines for Live-Cell Fluorescence Microscopy

被引:3
|
作者
Liu, Tianyan [1 ,2 ]
Kompa, Julian [3 ]
Ling, Jing [1 ,2 ]
Lardon, Nicolas [3 ]
Zhang, Yuan [1 ]
Chen, Jingting [1 ]
Reymond, Luc [4 ]
Chen, Peng [5 ,6 ]
Tran, Mai [3 ]
Yang, Zhongtian [1 ,2 ]
Zhang, Haolin [1 ,2 ]
Liu, Yitong [1 ,2 ]
Pitsch, Stefan [7 ]
Zou, Peng [2 ,8 ]
Wang, Lu [9 ]
Johnsson, Kai [3 ,4 ]
Chen, Zhixing [1 ,2 ,5 ,6 ]
机构
[1] Peking Univ, Inst Mol Med, Beijing Key Lab Cardiometab Mol Med, Coll Future Technol,Natl Biomed Imaging Ctr, Beijing 100871, Peoples R China
[2] Peking Univ, Acad Adv Interdisciplinary Studies, Peking Tsinghua Ctr Life Sci, State Key Lab Membrane Biol, Beijing 100871, Peoples R China
[3] Max Planck Inst Med Res, Dept Chem Biol, D-69120 Heidelberg, Germany
[4] Ecole Polytech Fed Lausanne EPFL, Biomol Screening Facil, CH-1015 Lausanne, Switzerland
[5] PKU Nanjing Inst Translat Med, Nanjing 211800, Peoples R China
[6] GenVivo Tech, Nanjing 211800, Peoples R China
[7] Spirochrome AG, Chalberweidstr 4, CH-8260 Stein, Switzerland
[8] Peking Univ, Coll Chem & Mol Engn, Synthet & Funct Biomol Ctr, Beijing Natl Lab Mol Sci,PKU IDG McGovern Inst Bra, Beijing 100871, Peoples R China
[9] Fudan Univ, Sch Pharm, Key Lab Smart Drug Delivery, Minist Educ, Shanghai 201203, Peoples R China
基金
国家重点研发计划;
关键词
GENERAL-METHOD; IMPROVE FLUOROPHORES; FLUOROGENIC PROBES; OXYGEN; PHOTOTOXICITY; PHOTODAMAGE; NANOSCOPY; CANCER; DYES;
D O I
10.1021/acscentsci.4c00616
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rhodamines have been continuously optimized in brightness, biocompatibility, and color to fulfill the demands of modern bioimaging. However, the problem of phototoxicity caused by the excited fluorophore under long-term illumination has been largely neglected, hampering their use in time-lapse imaging. Here we introduce cyclooctatetraene (COT) conjugated rhodamines that span the visible spectrum and exhibit significantly reduced phototoxicity. We identified a general strategy for the generation of Gentle Rhodamines, which preserved their outstanding spectroscopic properties and cell permeability while showing an efficient reduction of singlet-oxygen formation and diminished cellular photodamage. Paradoxically, their photobleaching kinetics do not go hand in hand with reduced phototoxicity. By combining COT-conjugated spirocyclization motifs with targeting moieties, these Gentle Rhodamines compose a toolkit for time-lapse imaging of mitochondria, DNA, and actin, and synergize with covalent and exchangeable HaloTag labeling of cellular proteins with less photodamage than their commonly used precursors. Taken together, the Gentle Rhodamines generally offer alleviated phototoxicity and allow advanced video recording applications, including voltage imaging.
引用
收藏
页码:1933 / 1944
页数:12
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