Fluorescent Probes for Sensing and Imaging within Specific Cellular Organelles

被引:838
作者
Zhu, Hao [1 ]
Fan, Jiangli [1 ]
Du, Jianjun [1 ]
Peng, Xiaojun [1 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
LARGE STOKES SHIFT; LIVING CELLS; LIVE CELLS; HIGH PHOTOSTABILITY; CANCER-CELLS; IN-VIVO; MITOCHONDRIA; SENSOR; VISCOSITY; DYE;
D O I
10.1021/acs.accounts.6b00292
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fluorescent probes have become powerful tools in biosensing and bioimaging because of their high sensitivity, specificity, fast response, and technical simplicity. In the last decades, researchers have made remarkable progress in developing fluorescent probes that respond to changes in microenvironments (e.g., pH, viscosity, and polarity) or quantities of biomolecules of interest (e.g., ions, reactive oxygen species, and enzymes). All of these analytes are specialized to carry out vital functions and are linked to serious disorders in distinct subcellular organelles. Each of these organelles plays a specific and indispensable role in cellular processes. For example, the nucleus regulates gene expression, mitochondria are responsible for aerobic metabolism, and lysosomes digest macromolecules, for cell recycling. A certain organelle requires specific biological species and the appropriate microenvironment to perform its cellular functions, while breakdown of the homeostasis of biomolecules or microenvironmental mutations leads to organelle malfunctions, which further cause disorders or diseases. Fluorescent probes that can be targeted to both specific organelles and biochemicals/microenvironmental factors are capable of reporting localized bioinformation and are potentially useful for gaining insight into the contributions of analytes to both healthy and diseased states. In this Account, we review our recent work on the development of fluorescent probes for sensing and imaging within specific organelles. We present an overview of the design, photophysical properties, and biological applications of the probes, which can localize to mitochondria, lysosomes, the nucleus, the Golgi apparatus, and the endoplasmic reticulum. Although a diversity of organelle-specific fluorescent stains have been commercially available, our efforts place an emphasis on improvements in terms of low cytotoxicity, high photostability, near-infrared (NIR) emission, two-photon excitation, and long fluorescence lifetimes, which are Crucial for long-time tracking of biological processes, tissue and body imaging with deep penetration and low autofluorescence, and time-resolved fluorescence imaging. Research on fluorescent probes with both analyte responsiveness and organelle targetability is a new and emerging area that has attracted increasing attention over the past few years. We have extended the diversity by developing organelle-specific responsive probes capable of detecting changes in biomolecular levels (reactive oxygen species, fluoride ion, hydrogen sulfide, zinc cation, thiol-containing amino acids, and cyclooxygenase-2) and the microenvironment (viscosity, polarity, and pH). Future research should give more considerations of the "low-concern" organelles, such as the Golgi apparatus, the endoplasmic reticulum, and ribosomes.. In addition, given the tiny sizes of subcellular organelles (20-1000 nm), we anticipate that clearer visulization of the cellular events within specific organelles will rely on super resolution optical microscopy with nanoscopic-scale resolution.
引用
收藏
页码:2115 / 2126
页数:12
相关论文
共 62 条
[1]   Cell biology - A role for lipid shells in targeting proteins to caveolae, rafts, and other lipid domains [J].
Anderson, RGW ;
Jacobson, K .
SCIENCE, 2002, 296 (5574) :1821-1825
[2]  
[Anonymous], 2011, ANGEW CHEM
[3]   γ-Interferon-inducible Lysosomal Thiol Reductase (GILT) Maintains Phagosomal Proteolysis in Alternatively Activated Macrophages [J].
Balce, Dale R. ;
Allan, Euan R. O. ;
McKenna, Neil ;
Yates, Robin M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (46) :31891-31904
[4]   Suppression of Mitochondrial Oxidative Phosphorylation and TCA Enzymes in Discrete Brain Regions of Mice Exposed to High Fluoride: Amelioration by Panax ginseng (Ginseng) and Lagerstroemia speciosa (Banaba) Extracts [J].
Basha, P. Mahaboob ;
Saumya, S. M. .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2013, 33 (03) :453-464
[5]   Mitochondria in the diabetic heart [J].
Bugger, Heiko ;
Abel, E. Dale .
CARDIOVASCULAR RESEARCH, 2010, 88 (02) :229-240
[6]   A highly specific BODIPY-based probe localized in mitochondria for HClO imaging [J].
Cheng, Guanghui ;
Fan, Jiangli ;
Sun, Wen ;
Sui, Kun ;
Jin, Xin ;
Wang, Jingyun ;
Peng, Xiaojun .
ANALYST, 2013, 138 (20) :6091-6096
[7]   ROS as signalling molecules:: mechanisms that generate specificity in ROS homeostasis [J].
D'Autreaux, Benoit ;
Toledano, Michel B. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2007, 8 (10) :813-824
[8]   A targetable fluorescent probe for imaging hydrogen peroxide in the mitochondria of living cells [J].
Dickinson, Bryan C. ;
Chang, Christopher J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (30) :9638-+
[9]   Mitochondrial-targeted fluorescent probes for reactive oxygen species [J].
Dickinson, Bryan C. ;
Srikun, Duangkhae ;
Chang, Christopher J. .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2010, 14 (01) :50-56
[10]   A Targetable Fluorescent Sensor Reveals That Copper-Deficient SCO1 and SCO2 Patient Cells Prioritize Mitochondrial Copper Homeostasis [J].
Dodani, Sheel C. ;
Leary, Scot C. ;
Cobine, Paul A. ;
Winge, Dennis R. ;
Chang, Christopher J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (22) :8606-8616