4.8 Article

Nucleic acid-functionalized metal-organic framework for ultrasensitive immobilization-free photoelectrochemical biosensing

Journal

BIOSENSORS & BIOELECTRONICS
Volume 173, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2020.112832

Keywords

Photoelectrochemical biosensors; Aptamer; Carcinoembryonic antigen detection; Nucleic acid-functionalized metal-organic frameworks; Exonuclease-assisted recycling amplification

Funding

  1. National Natural Science Foundation of China [21775083, 21775082]
  2. Special Foundation for Distinguished Taishan Scholar of Shandong Province [ts201511052]
  3. Major Program of Shandong Province Natural Science Foundation [ZR2018ZC0127]

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This study presents an immobilization-free PEC biosensor for ultrasensitive determination of CEA, utilizing DNA-functionalized MOFs and T7 exonuclease-assisted recycling amplification. The biosensor shows a low detection limit, wide linear range, high selectivity for CEA detection, and great potential for application in bioanalysis and early disease diagnosis.
This work established an immobilization-free photoelectrochemical (PEC) biosensor for ultrasensitive determination of carcinoembryonic antigen (CEA) based on the DNA-functionalized metal-organic frameworks (MOFs) and T7 exonuclease-aided recycling amplification. In this proposal, MOFs were served as nanocarriers for efficient encapsulation of electron donors, while an ingeniously designed hairpin probe (HP) employed as the recognition element. The recognition of CEA by its aptamer sequence in HP triggered the conformational change and the T7 exonuclease-aided recycling amplification, which opened the pore of MOFs to release a large number of electron donors, producing a significantly increased photocurrent. Benefitting from the high loading ability of MOFs and the excellent amplification efficiency of the T7 exonuclease-assisted recycling process, the proposed biosensor is capable of ultrasensitive and highly selective determination of CEA with a detection limit down to 0.36 fg mL(-1) and a wide linear range from 1.0 fg mL(-1) to 10 ng mL(-1). Moreover, the proposed biosensor can also apply to measure CEA in spiked serum samples, indicating that this PEC biosensor holds excellent potential for application in bioanalysis and early disease diagnosis.

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