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
相关论文
共 50 条
  • [11] Live-cell microscopy - tips and tools
    Frigault, Melanie M.
    Lacoste, Judith
    Swift, Jody L.
    Brown, Claire M.
    JOURNAL OF CELL SCIENCE, 2009, 122 (06) : 753 - 767
  • [12] Live-cell microscopy of meiosis in spermatocytes
    Shibuya, Hiroki
    Watanabe, Yoshinori
    MITOSIS AND MEIOSIS, PT B, 2018, 145 : 269 - 277
  • [13] QUANTITATIVE COMPARISON OF SPOT DETECTION METHODS IN LIVE-CELL FLUORESCENCE MICROSCOPY IMAGING
    Smal, Ihor
    Loog, Marco
    Niessen, Wiro
    Meijering, Erik
    2009 IEEE INTERNATIONAL SYMPOSIUM ON BIOMEDICAL IMAGING: FROM NANO TO MACRO, VOLS 1 AND 2, 2009, : 1178 - +
  • [14] Live-cell imaging of macrophage phagocytosis of asbestos fibers under fluorescence microscopy
    Takenori Ishida
    Nobutoshi Fujihara
    Tomoki Nishimura
    Hisakage Funabashi
    Ryuichi Hirota
    Takeshi Ikeda
    Akio Kuroda
    Genes and Environment, 41
  • [15] Live-Cell Fluorescence Microscopy with Molecular Biosensors: What Are We Really Measuring?
    Haugh, Jason M.
    BIOPHYSICAL JOURNAL, 2012, 102 (09) : 2003 - 2011
  • [16] Dynamics of Intracellular Processes in Live-Cell Systems Unveiled by Fluorescence Correlation Microscopy
    Gonzalez Bardeci, Nicolas
    Francisco Angiolini, Juan
    Cecilia De Rossi, Maria
    Bruno, Luciana
    Levi, Valeria
    IUBMB LIFE, 2017, 69 (01) : 8 - 15
  • [17] ENERGY MINIMIZATION METHODS FOR CELL MOTION CORRECTION AND INTRACELLULAR ANALYSIS IN LIVE-CELL FLUORESCENCE MICROSCOPY
    Dzyubachyk, Oleh
    van Cappellen, Wiggert A.
    Essers, Jeroen
    Niessen, Wiro
    Meijering, Erik
    2009 IEEE INTERNATIONAL SYMPOSIUM ON BIOMEDICAL IMAGING: FROM NANO TO MACRO, VOLS 1 AND 2, 2009, : 1127 - +
  • [18] Live-Cell Fluorescence Microscopy to Investigate Subcellular Protein Localization and Cell Morphology Changes in Bacteria
    Brzozowski, Robert S.
    White, Maria L.
    Eswara, Prahathees J.
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2019, (153):
  • [19] Sparse deconvolution improves the resolution of live-cell super-resolution fluorescence microscopy
    Zhao, Weisong
    Zhao, Shiqun
    Li, Liuju
    Huang, Xiaoshuai
    Xing, Shijia
    Zhang, Yulin
    Qiu, Guohua
    Han, Zhenqian
    Shang, Yingxu
    Sun, De-En
    Shan, Chunyan
    Wu, Runlong
    Gu, Lusheng
    Zhang, Shuwen
    Chen, Riwang
    Xiao, Jian
    Mo, Yanquan
    Wang, Jianyong
    Ji, Wei
    Chen, Xing
    Ding, Baoquan
    Liu, Yanmei
    Mao, Heng
    Song, Bao-Liang
    Tan, Jiubin
    Liu, Jian
    Li, Haoyu
    Chen, Liangyi
    NATURE BIOTECHNOLOGY, 2022, 40 (04) : 606 - +
  • [20] Live-cell Microscopy and Fluorescence-based Measurement of Luminal pH in Intracellular Organelles
    Ma, Li
    Ouyang, Qing
    Werthmann, Gordon C.
    Thompson, Heather M.
    Morrow, Eric M.
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2017, 5