A multi-recycling amplification-based sensor for label-free and highly sensitive detection of telomerase from cancer cells

被引:6
作者
Liu, Xiaoxia [1 ]
Li, Xia [1 ]
Li, Jin [2 ]
Jiang, Bingying [2 ]
Yuan, Ruo [1 ]
Xiang, Yun [1 ]
机构
[1] Southwest Univ, Sch Chem & Chem Engn, Key Lab Luminescent & Real Time Analyt Chem, Minist Educ, Chongqing 400715, Peoples R China
[2] Chongqing Univ Technol, Sch Chem & Chem Engn, Chongqing 400054, Peoples R China
基金
中国国家自然科学基金;
关键词
Telomerase; Nicking endonuclease; Cascade recycling cycles; G-quadruplex; Fluorescence; ELECTROCHEMICAL BIOSENSOR; ULTRASENSITIVE DETECTION; MOLECULAR BEACON; FLUORESCENCE; NANOPARTICLES; INTEGRATION; GRAPHENE;
D O I
10.1016/j.aca.2019.08.033
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The development of methods that can detect telomerase with high selectivity and sensitivity is critical for early diagnosis and treatment of telomerase-related cancers. In this regard, we describe in this work the establishment of a telomerase-initiated and nicking endonuclease-assisted cascade recycling signal amplification approach for non-label and highly sensitive fluorescent detection of telomerase from cancer cells. The target telomerase triggers the elongation of one strand in a partial dsDNA duplex with a pre-designed sequence to induce the release of a ssDNA, which can initiate three cascaded recycling cycles for the generation of many G-quadruplex sequences by cleaving two hairpin signal probes with the assistance of the Nt.AlwI endonuclease. The thioflavin dye further binds these G-quadruplex sequences to exhibit substantial fluorescence enhancement for sensitive detection of telomerase at 8.93 x 10(-11) IU. Moreover, this developed method is capable of differentiating telomerase activity among different cancer cells and screening telomerase inhibitors for anticancer drugs. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:116 / 121
页数:6
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