Nanoscale Zeolitic Imidazolate Framework-8 for Ratiometric Fluorescence Imaging of MicroRNA in Living Cells

被引:142
作者
Yi, Jin-Tao [1 ]
Chen, Ting-Ting [1 ]
Huo, Jia [1 ]
Chu, Xia [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC-FRAMEWORK; DRUG-DELIVERY; IN-VITRO; CANCER; EXPRESSION; GOLD; NANOPARTICLES; PROLIFERATION; STORAGE; DNAZYME;
D O I
10.1021/acs.analchem.7b03369
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
MicroRNAs (miRNAs) play important roles in cell differentiation, proliferation, and apoptosis and have been recognized as valuable biomarkers for clinical disease diagnosis. Here, we adopt for the first time zeolitic imidazolate framework-8 (ZIF-8) as a nanocarrier to efficiently deliver a nucleic acid probe to living cells and develop a novel ratiometric fluorescence strategy based on DNAzyme for miRNA-21 imaging. A Cy5-labeled 8-17 DNAzyme strand and a Cy3-labeled substrate strand containing a segment complementary to the target miRNA-21 first form a duplex probe, and fluorescence resonance energy transfer (FRET) takes place. After adsorption on the ZIF-8 surface and cellular uptake, the probe/ZIF-8 nanocomplex degrades in acidic endosome and releases duplex probes and Zn2+, and the latter can act as an effective cofactor for 8-17 DNAzyme. The intracellular miRNA-21 hybridizes with the complementary segment of the substrate strand and results in dissociation from the DNAzyme substrate duplex probe after DNAzyme cleaves the substrate into two fragments, accompanied by the change in the FRET signal. The proposed method has been applied to image miRNA-21 expression levels in MCF-7, HeLa, and L02 cells with high contrast and reliability. The fluctuation of miRNA-21 expression level induced by miRNA-21 mimic or inhibitor can also be monitored through the obvious imaging color change. Taken together, the proposed method provides a powerful tool for cancer diagnosis and miRNA-associated biological study.
引用
收藏
页码:12351 / 12359
页数:9
相关论文
共 51 条
[1]   Luminescent metal-organic frameworks [J].
Allendorf, M. D. ;
Bauer, C. A. ;
Bhakta, R. K. ;
Houk, R. J. T. .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (05) :1330-1352
[2]   A lead-dependent DNAzyme with a two-step mechanism [J].
Brown, AK ;
Li, J ;
Pavot, CMB ;
Lu, Y .
BIOCHEMISTRY, 2003, 42 (23) :7152-7161
[3]   Aptamer-Conjugated Graphene Quantum Dots/Porphyrin Derivative Theranostic Agent for Intracellular Cancer-Related MicroRNA Detection and Fluorescence-Guided Photothermal/Photodynamic Synergetic Therapy [J].
Cao, Yu ;
Dong, Haifeng ;
Yang, Zhou ;
Zhong, Xiangmin ;
Chen, Yi ;
Dai, Wenhao ;
Zhang, Xueji .
ACS APPLIED MATERIALS & INTERFACES, 2017, 9 (01) :159-166
[4]   MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells [J].
Chan, JA ;
Krichevsky, AM ;
Kosik, KS .
CANCER RESEARCH, 2005, 65 (14) :6029-6033
[5]   The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation [J].
Chen, JF ;
Mandel, EM ;
Thomson, JM ;
Wu, QL ;
Callis, TE ;
Hammond, SM ;
Conlon, FL ;
Wang, DZ .
NATURE GENETICS, 2006, 38 (02) :228-233
[6]   Highly selective detection of microRNA based on distance-dependent electrochemiluminescence resonance energy transfer between CdTe nanocrystals and Au nanoclusters [J].
Cheng, Yan ;
Lei, Jianping ;
Chen, Yunlong ;
Ju, Huangxian .
BIOSENSORS & BIOELECTRONICS, 2014, 51 :431-436
[7]   Multifunctional Poly(L-lactide)-Polyethylene Glycol-Grafted Graphene Quantum Dots for Intracellular MicroRNA Imaging and Combined Specific-Gene-Targeting Agents Delivery for Improved Therapeutics [J].
Dong, Haifeng ;
Dai, Wenhao ;
Ju, Huangxian ;
Lu, Huiting ;
Wang, Shiyan ;
Xu, Liping ;
Zhou, Shu-Feng ;
Zhang, Yue ;
Zhang, Xueji .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (20) :11015-11023
[8]  
Farha OK, 2010, NAT CHEM, V2, P944, DOI [10.1038/NCHEM.834, 10.1038/nchem.834]
[9]  
Horcajada P, 2010, NAT MATER, V9, P172, DOI [10.1038/NMAT2608, 10.1038/NMAT260B, 10.1038/nmat2608]
[10]   The let-7 MicroRNA represses cell proliferation pathways in human cells [J].
Johnson, Charles D. ;
Esquela-Kerscher, Aurora ;
Stefani, Giovanni ;
Byrom, Nlike ;
Kelnar, Kevin ;
Ovcharenko, Dmitriy ;
Wilson, Mike ;
Wang, Xiaowei ;
Shelton, Jeffrey ;
Shingara, Jaclyn ;
Chin, Lena ;
Brown, David ;
Slack, Frank J. .
CANCER RESEARCH, 2007, 67 (16) :7713-7722