Abstract
Type I topoisomerases (TOPOI), a potential diagnostic biomarker and a target for chemotherapeutic agents, play essential roles in DNA replication, transcription, chromosome segregation, and recombination. It is essential to develop analytical methods for accurate detection of TOPOI in biological fluids for early diagnosis of diseases. Here we show an assay for TOPOI on the basis of the target-induced self-assembly of graphene oxide (GO) sheets onto hydroxycamptothecin-functionalized upconversion nanoparticles (HCPT-UCNPs). The dipole-dipole coupling of HCPT-UCNPs (donor) and GO (acceptor) regulated by TOPOI enables Förster resonance energy transfer between the donor and the acceptor. Integration of minimal autofluorescence and highly specific affinity into the developed nanosensor allows reliable detection of TOPOI in the nanomolar range with the detection limit of 0.29 nM. The detection of TOPOI in breast cancer cells with recoveries from 96.3 to 103.7% shows the availability of the proposed assay in complicated samples.
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Funding
This study received financial support from the National Natural Science Foundation of China (Nos. 21435001 and 81401471), the China Postdoctoral Science Foundation (No. 2015 M581306), the Natural Science Foundation of Tianjin (No. 17JCYBJC20700), the Natural Science Foundation of Tianjin Medical University (No. 2014KYQ14), and the National First-class Discipline Program of Food Science and Technology (No. JUFSTR20180301).
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Published in the topical collection New Insights into Analytical Science in China with guest editors Lihua Zhang, Hua Cui, and Qiankun Zhuang.
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Wang, X., Yan, XP. Analyte-driven self-assembly of graphene oxide sheets onto hydroxycamptothecin-functionalized upconversion nanoparticles for the determination of type I topoisomerases in cell extracts. Anal Bioanal Chem 410, 6761–6769 (2018). https://doi.org/10.1007/s00216-018-1234-0
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DOI: https://doi.org/10.1007/s00216-018-1234-0