A dual-colored ratiometric-fluorescent oligonucleotide probe for the detection of human telomerase RNA in cell extracts

被引:15
作者
Ning, Dianhua [1 ,2 ]
He, Changtian [1 ,2 ]
Liu, Zhengjie [1 ,2 ]
Liu, Cui [1 ,2 ]
Wu, Qilong [1 ,2 ]
Zhao, TingTing [1 ,3 ]
Liu, Renyong [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Intelligent Machines, Hefei 230031, Anhui, Peoples R China
[2] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China
[3] Chinese Acad Sci, State Key Lab Transducer Technol, Hefei 230031, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
RESONANCE ENERGY-TRANSFER; MESSENGER-RNA; QUANTUM DOTS; DNA; CANCER; HTERT; FRET; HTR; ELECTROPHORESIS; NANOFLARES;
D O I
10.1039/c7an00150a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Human telomerase RNA (hTR), which is one component of telomerase, was deemed to be a biomarker to monitor tumor cells due to its different expression levels in tumor cells and normal somatic cells. Thus far, plentiful fluorescent probes have been designed to investigate nucleic acids. However, most of them are limited since they are time-consuming, require professional operators and even result in false positive signals in the cellular environment. Herein, we report a dual-colored ratiometric-fluorescent oligonucleotide probe to achieve the reliable detection of human telomerase RNA in cell extracts. The probe is constructed using a dual-labeled fluorescent oligonucleotide hybridized with target-complemented Dabcyl-labeled oligonucleotide. In the presence of the target, the dual-labeled fluorescent oligonucleotide translates into a hairpin structure, which leads to the generation of the fluorescence resonance energy transfer (FRET) phenomenon under UV excitation. Compared to conventional methods, this strategy could effectively avoid false positive signals, and it not only possesses the advantages of simplicity and high specificity but also has the merits of signal stability and distinguishable color variation. Moreover, the quantitative assay of hTR would have a far-reaching impact on the telomerase mechanism and even tumor diagnosis research.
引用
收藏
页码:1697 / 1702
页数:6
相关论文
共 45 条
[1]   Quantitative assessment of telomerase components in cancer cell lines [J].
Akincilar, Semih Can ;
Low, Kee Chung ;
Liu, Chia Yi ;
Yan, Ting Dong ;
Oji, Asami ;
Ikawa, Masahito ;
Li, Shang ;
Tergaonkar, Vinay .
FEBS LETTERS, 2015, 589 (09) :974-984
[2]  
Avilion AA, 1996, CANCER RES, V56, P645
[3]   ARCHITECTURE OF TELOMERASE RNA [J].
BHATTACHARYYA, A ;
BLACKBURN, EH .
EMBO JOURNAL, 1994, 13 (23) :5721-5731
[4]   STRUCTURE AND FUNCTION OF TELOMERES [J].
BLACKBURN, EH .
NATURE, 1991, 350 (6319) :569-573
[5]   Telomere shortening and tumor formation by mouse cells lacking telomerase RNA [J].
Blasco, MA ;
Lee, HW ;
Hande, MP ;
Samper, E ;
Lansdorp, PM ;
DePinho, RA ;
Greider, CW .
CELL, 1997, 91 (01) :25-34
[6]   Telomerase redefined: Integrated regulation of hTR and hTERT for telomere maintenance and telomerase activity [J].
Cairney, C. J. ;
Keith, W. N. .
BIOCHIMIE, 2008, 90 (01) :13-23
[7]   Increased copy number of the TERT and TERC telomerase subunit genes in cancer cells [J].
Cao, Ying ;
Bryan, Tracy M. ;
Reddel, Roger R. .
CANCER SCIENCE, 2008, 99 (06) :1092-1099
[8]   Simultaneous non-invasive analysis of DNA condensation and stability by two-step QD-FRET [J].
Chen, Hunter H. ;
Ho, Yi-Ping ;
Jiang, Xuan ;
Mao, Hai-Quan ;
Wang, Tza-Huei ;
Leong, Kam W. .
NANO TODAY, 2009, 4 (02) :125-134
[9]   Single-Stranded DNA Assisted Cell Penetrating Peptide-DNA Conjugation Strategy for Intracellular Imaging of Nucleases [J].
Chen, Lu ;
Fang, Simin ;
Xiao, Xianjin ;
Zheng, Bo ;
Zhao, Meiping .
ANALYTICAL CHEMISTRY, 2016, 88 (23) :11306-11309
[10]   Enzyme-free detection of DNA based on hybridization chain reaction amplification and fluorescence resonance energy transfer [J].
Chen, Ying ;
Chen, Ling ;
Ou, Yidian ;
Guo, Liangqia ;
Fu, Fengfu .
SENSORS AND ACTUATORS B-CHEMICAL, 2016, 233 :691-696