Monitoring Dynamic Cellular Redox Homeostasis Using Fluorescence-Switchable Graphene Quantum Dots

被引:65
作者
Li, Nan [1 ]
Than, Aung [1 ]
Sun, Chencheng [2 ,3 ]
Tian, Jingqi [1 ]
Chen, Jie [1 ]
Pu, Kanyi [1 ]
Dong, Xiaochen [2 ,3 ]
Chen, Peng [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Div Bioengn, 70 Nanyang Dr, Singapore 637457, Singapore
[2] Nanjing Tech Univ NanjingTech, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, Key Lab Flexible Elect KLOFE, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[3] Nanjing Tech Univ NanjingTech, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, Inst Adv Mat, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
关键词
graphene quantum dots; redox homeostasis; fluorescent probes; live cell imaging; CARBON NANOMATERIALS; EMERGENT NANOLIGHTS; HYDROGEN-PEROXIDE; VITAMIN-C; IMBALANCE; CELLS; CANCER; PROBES; LIVE; GLUTATHIONE;
D O I
10.1021/acsnano.6b07237
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Monitoring cellular redox homeostasis is critical to the understanding of many physiological functions ranging from immune reactions to metabolism, as well as to the understanding of pathological development ranging from tumorigenesis to aging. Nevertheless, there is currently a lack of appropriate probes for this ambition, which should be reversibly, sensitively, and promptly responsive to a wide range of physiological oxidants and reductants. In this work, a redox-sensitive fluorescence-switchable probe is designed based on graphene quantum dots (GQDs) functionalized with a chelated redox Fe2+/Fe3+ couple. The underlying mechanism is investigated and discussed. The high sensitivity and fast response are attributable to the fact that the GQD's photoluminescence is highly sensitive to photon-induced electron transfer because of its ultrasmall size and associated prominent quantum confinement effect. Also taking advantages of GQDs' excellent photostability, biocompatibility, and readiness for cell uptake, our reversibly tunable fluorescence probe is employed to monitor in real time the triggered dynamic change of the intracellular redox state. This addition to the limited arsenal of available redox probes shall be useful to the still poorly understood redox biology, as well as for monitoring environment or chemical processes involving redox reactions.
引用
收藏
页码:11475 / 11482
页数:8
相关论文
共 52 条
[1]   Oxidant/Antioxidant Imbalance and the Risk of Alzheimer's Disease [J].
Abdel Moneim, Ahmed E. .
CURRENT ALZHEIMER RESEARCH, 2015, 12 (04) :335-349
[2]   Interaction of Graphene Quantum Dots with 4-Acetamido-2,2,6,6-Tetramethylpiperidine-Oxyl Free Radicals: A Spectroscopic and Fluorimetric Study [J].
Achadu, Ojodomo J. ;
Nyokong, Tebello .
JOURNAL OF FLUORESCENCE, 2016, 26 (01) :283-295
[3]  
[Anonymous], 1980, PHOTOVOLTAIC PHOTOEL, P266, DOI [10.1007/978-1-4615-9233-4, DOI 10.1007/978-1-4615-9233-4]
[4]   Luminescent Carbon Nanodots: Emergent Nanolights [J].
Baker, Sheila N. ;
Baker, Gary A. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (38) :6726-6744
[5]   Carbon nanomaterials: multi-functional agents for biomedical fluorescence and Raman imaging [J].
Bartelmess, J. ;
Quinn, S. J. ;
Giordani, S. .
CHEMICAL SOCIETY REVIEWS, 2015, 44 (14) :4672-4698
[6]  
Bisquert S. G. J., 2016, PHOTOELECTROCHEMICAL, P12, DOI [10.1007/978-3-319-2964-8, DOI 10.1007/978-3-319-2964-8]
[7]   THE OXIDATION-REDUCTION REACTIONS OF HYDROGEN PEROXIDE AT INERT METAL ELECTRODES AND MERCURY CATHODES [J].
BOCKRIS, JO ;
OLDFIELD, LF .
TRANSACTIONS OF THE FARADAY SOCIETY, 1955, 51 (02) :249-259
[8]   Oxidation reduction potential of ascorbic acid (Vitamin C) [J].
Borsook, H ;
Keighley, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1933, 19 :875-878
[9]  
Brown G.M., 2006, PERCHLORATE, P17, DOI DOI 10.1016/j.atmosenv.2010.07.057
[10]   REACTIVE OXYGEN SPECIES (ROS) - A FAMILY OF FATE DECIDING MOLECULES PIVOTAL IN CONSTRUCTIVE INFLAMMATION AND WOUND HEALING [J].
Bryan, Nicholas ;
Ahswin, Helen ;
Smart, Neil ;
Bayon, Yves ;
Wohlert, Stephen ;
Hunt, John A. .
EUROPEAN CELLS & MATERIALS, 2012, 24 :249-265