4.8 Article

Nanoscaled Porphyrinic Metal-Organic Frameworks for Electrochemical Detection of Telomerase Activity via Telomerase Triggered Conformation Switch

Journal

ANALYTICAL CHEMISTRY
Volume 88, Issue 21, Pages 10680-10686

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.6b03131

Keywords

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Funding

  1. National Natural Science Foundation of China [21375060, 21135002, 21675084]
  2. Priority development areas of the National Research Foundation for the Doctoral Program of Higher Education of China [20130091130005]

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In this work, we designed a nanoscaled porphyrinic metal-organic framework (PorMOF) with iron porphyrin as linker and zirconium ion as node for electrochemical detection of telomerase activity. The as-prepared PorMOF was characterized with scanning electron microscopy, powder X-ray diffraction, and spectroscopic techniques and demonstrated excellent electrocatalytic activity toward O2 reduction. Sequentially, the functionalization of PorMOF with streptavidin results in a water-stable electrochemical tracer for detection of telomerase. Upon the telomerase-triggered extension, the assistant DNA 1 (aDNA1)-assistant DNA 2 (aDNA2) duplex could switch into a hairpin structure, and thus, the aDNA2 was released and then hybridized with the capture DNA. Therefore, the PorMOF@SA tracer could be introduced on the electrode surface via biotin-streptavidin recognition, leading to the strong electrochemical signal for readout. The developed approach displayed desirable dynamic range and limitation of detection down to 30 HeLa cells mL-1. The telomerase activity was 2.2 X 10(-11) IU in a single HeLa cell with good reproducibility and stability. The nanoscaled porphyrinic MOF provided a powerful platform for electrochemical signal transduction and had a promising application in the determination of various biomolecules.

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