Manifold methods for telomerase activity detection based on various unique probes

被引:18
作者
Wang, Chunlei [1 ]
Yang, Haitang [1 ]
Wu, Shuangshuang [1 ]
Liu, Yuanjian [1 ]
Wei, Wei [1 ]
Zhang, Yuanjian [1 ]
Wei, Min [2 ]
Liu, Songqin [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Jiangsu Engn Lab Smart Carbon Rich Mat & Device, Jiangsu Prov Hitech Key Lab Biomed Res, Nanjing 211189, Jiangsu, Peoples R China
[2] Henan Univ Technol, Coll Food Sci & Technol, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Telomerase; Tumor biomarker; Colorimetric; Fluorescence; Electrochemistry; Electrochemiluminescence; Surface enhanced Raman scattering; Chemiluminescence; Nanoprobe; Nanoparticle; METAL-ORGANIC FRAMEWORKS; FREE ULTRASENSITIVE DETECTION; INTRACELLULAR TELOMERASE; ELECTROCHEMICAL DETECTION; GOLD NANOPARTICLES; AU NANOPARTICLES; BLADDER-CANCER; REAL-TIME; DNA; AMPLIFICATION;
D O I
10.1016/j.trac.2018.06.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Telomerase is a basic nuclear protein reverse transcriptase and responsible for the elongation of telomeres in cells. It has attracted a lot of attentions and acted as an important sally port for cancer diagnosis and clinical therapy. Hence, accurate and efficient determination of telomerase activity is significant. In recent years, numerous sensitive and accurate techniques have been developed for in vitro or in situ detection of telomerase activity. These methods were mainly dependent on three unique properties of elongated telomerase primer (TS primer): 1) Plenty of negative charges play important role to change interactions between biomolecules and signal probes; 2) G-rich sequences have excellent peroxidase-like catalytic activity; 3) They can be used for DNA hybridization or strand displacement reaction, which are beneficial to construct biosensors. In this review, we conclude and enumerate these advanced methods for telomerase activity detection in recent years. Development trends of telomerase detection are also prospected. (c) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:404 / 412
页数:9
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