期刊
ANALYTICA CHIMICA ACTA
卷 1097, 期 -, 页码 135-143出版社
ELSEVIER
DOI: 10.1016/j.aca.2019.10.069
关键词
Fluorescence; Telomerase; Signal amplification; Metal enhanced fluorescence; Graphene oxide; Gold nanoparticles
资金
- National Natural Science Foundation of China [21675078, 21475056, 21105044]
- Natural Science Foundation of Jiangxi Province [20165BCB18022, 20171BAB203016, 2018ACB21008]
- Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education
Telomerase, as a potential biomarker for early cancer diagnostics and therapies, has attracted considerable interests concerning its detection and monitoring. Herein, we develop a novel method for sensitive detection of telomerase activity by designing a gold nanoparticles/graphene oxide (AuNPs/GO) probe. The AuNPs were functionalized with a telomerase substrate (TS) primer and a 6-carboxy-fluorescein (FAM)-modified complementary DNA (P1). In the absence of telomerase, P1 exists in the randomcoiled conformation, and the fluorescence resonance energy transfer (FRET) from FAM to AuNPs and GO results in efficient fluorescence quenching. In the presence of telomerase, the multiple hybridization between TS extension products and P1 leads to the conformation transition of P1 from single-stranded DNA to double-stranded rigid structure, and thus the FRET process can be prevented with the efficient fluorescence recovery. The metal enhanced fluorescence (MEF) effect between FAM and AuNPs can further effectively enhance the fluorescence of FAM, and thus the sensitivity and specificity of telomerase detection can be remarkably improved. It is worth mentioning that the proposed strategy does not need to design complex hairpin structure and allows the measurement of telomerase activity in three crude cell extracts equivalent to 7 HeLa cells, 8 A549 cells and 8 L929 cells in 1 h. In addition, the present sensing platform can be applied to inhibitor screening, in situ telomerase imaging, and intracellular drug delivery. (C) 2019 Elsevier B.V. All rights reserved.
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