ATP-triggered highly sensitive probes for super-resolution mitochondrial imaging and low-dose bioimaging

被引:6
作者
Han, Taihe [1 ]
Zhang, Jinlong [1 ]
Mu, Shuai [2 ]
Li, Huihui [3 ]
Wu, Shuangtong [1 ]
Liu, Xiaoyan [1 ]
Zhang, Haixia [1 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Coll Vet Med, State Key Lab Vet Etiol Biol, Lanzhou 730000, Peoples R China
[3] Hainan Univ, Coll Sci, Key Lab Adv Mat Trop Isl Resources, Minist Educ, Haikou 570228, Peoples R China
基金
中国国家自然科学基金;
关键词
ADENOSINE 5'-TRIPHOSPHATE; GENERAL-METHOD; LIVE-CELL; FLUOROPHORES; FLUORESCENCE; SYSTEM; DYES;
D O I
10.1039/d3tb00534h
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Adenosine triphosphate (ATP), mainly produced in mitochondria, plays an important role in various pathological processes such as inflammation and acute liver injury. Fluorescence imaging is a powerful tool for imaging tissue structure and function in vivo. To date, the lack of biocompatible ATP probes with bright fluorescence emission has hindered their application in basic research and clinical trials. Here, we report a method for preparing ATP probes using a ZIF-90 potting dye, which produces bright ATP probes by encapsulating a modified high fluorescence quantum yield dye into a ZIF-90 skeleton. The nanoprobe does not fluoresce due to the coating. ATP can cooperate with Zn2+ to decompose the nanoprobe structure, release the dye and restore the fluorescence. Both nanoprobes ORhBSO2@ZIF-90 and SiRhBSO2@ZIF-90 showed higher sensitivity than the reported ATP nanoprobes with detection limits of 7.56 mu M and 6.6 mu M, and with lower doses (10 mu g mL(-1)) of probes for cell imaging. In addition, SiRhBSO2@ZIF-90 has also been successfully used in the liver injury model. The ZIF-90 encapsulation strategy can retain the high fluorescence quantum yield and improve the biocompatibility of the dye.
引用
收藏
页码:4776 / 4784
页数:9
相关论文
共 34 条
[1]   Cystic fibrosis transmembrane conductance regulator and adenosine triphosphate [J].
Abraham, EH ;
Okunieff, P ;
Scala, S ;
Vos, P ;
Oosterveld, MJS ;
Chen, AY ;
Shrivastav, B ;
Guidotti, G .
SCIENCE, 1997, 275 (5304) :1324-1325
[2]   Adenosine 5′-triphosphate and adenosine as endogenous signaling molecules in immunity and inflammation [J].
Bours, M. J. L. ;
Swennen, E. L. R. ;
Di Virgilio, F. ;
Cronstein, B. N. ;
Dagnelie, P. C. .
PHARMACOLOGY & THERAPEUTICS, 2006, 112 (02) :358-404
[3]   Mitochondria Targeted Nanoscale Zeolitic Imidazole Framework-90 for ATP Imaging in Live Cells [J].
Deng, Jingjing ;
Wang, Kai ;
Wang, Ming ;
Yu, Ping ;
Mao, Lanqun .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (16) :5877-5882
[4]   Mammalian TOR: A homeostatic ATP sensor [J].
Dennis, PB ;
Jaeschke, A ;
Saitoh, M ;
Fowler, B ;
Kozma, SC ;
Thomas, G .
SCIENCE, 2001, 294 (5544) :1102-1105
[5]  
Di Virgilio F., 2003, DRUG DEVELOP RES, V59, P171
[6]   Cisplatin induces acute renal failure by impairing antioxidant system in guinea pigs:: Effects of antioxidant supplementation on the cisplatin nephrotoxicity [J].
Durak, I ;
Özbek, H ;
Karaayvaz, M ;
Öztürk, HS .
DRUG AND CHEMICAL TOXICOLOGY, 2002, 25 (01) :1-8
[7]   MECHANISMS OF DISEASE Purinergic Signaling during Inflammation [J].
Eltzschig, Holger K. ;
Sitkovsky, Michail V. ;
Robson, Simon C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (24) :2322-2333
[8]  
Grimm JB, 2017, NAT METHODS, V14, P987, DOI [10.1038/NMETH.4403, 10.1038/nmeth.4403]
[9]  
Grimm JB, 2016, NAT METHODS, V13, P985, DOI [10.1038/NMETH.4034, 10.1038/nmeth.4034]
[10]  
Grimm JB, 2015, NAT METHODS, V12, P244, DOI [10.1038/NMETH.3256, 10.1038/nmeth.3256]