4.7 Article

Hybridization chain reaction coupled with the fluorescence quenching of gold nanoparticles for sensitive cancer protein detection

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 243, Issue -, Pages 731-737

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2016.12.047

Keywords

Anterior gradient homolog 2; AGR2 aptamer; Hairpin DNA; Fluorescence Gold nanoparticles; Hybridization chain reaction

Funding

  1. National Natural Science Foundation of China [21305053]
  2. The Research Innovation Program for College Graduates of Jiangsu Province [KYZZ16_0468]

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An ultrasensitive and enzyme-free sensing platform was designed for sensitive detection of anterior gradient homolog 2 (AGR2) based on the fluorescence quenching of gold nanoparticles (AuNPs) coupled with hybridization chain reaction (HCR) amplification. To construct the sensor, two fluorophore labeled hairpin probes (HP1 and HP2) that contained the sticky tails were designed, and AGR2 aptamer was used as an initiator for the happen of HCR between HP1 and HP2 to form a long nicked dsDNA duplex. Such DNA duplex could not adsorb onto the surface of AuNPs, and a strong fluorescence signal appeared due to the label of HP1 and HP2 with fluorophore. In the presence of AGR(2), AGR(2) aptamer would specifically recognize with it and accordingly could not trigger the happen of HCR. As a result, the sticky tails of HP1 and HP2 would adsorb onto the surface of AuNPs to bring the fluorophore into the close proximity of the AuNPs, and lead to the quenching of the fluorescence signal. By using such method, AGR(2) could be sensitively detected in the range of 5.0 pM-1.0 nM based on monitoring the decrease of the fluorescence signal. Importantly, the assay could realize the detection of AGR2 effectively in diluted human serum samples. (C) 2016 Elsevier B.V. All rights reserved.

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