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Proximity hybridization-induced on particle DNA walker for ultrasensitive protein detection.

Abstract
A simple proximity hybridization-induced on particle DNA walker was designed for ultrasensitive detection of proteins, for example platelet-derived growth factor (PDGF-BB) secreted by cancer cells, in which the DNA walker was activated by specific target binding and powered by an enzymatic cleavage to produce amplified signal. High-density FAM-labeled hairpin oligonucleotides (FAM-DNA1) were functionalized on AuNPs to construct three-dimensional (3D) DNA tracks. The specific binding of PDGF-BB with two aptamer probes (DNA3 and DNA4) led to the proximity hybridization-induced DNA displacement and the free of DNA walker (DNA2) to perform movement on the 3D tracks by an enzymatic cleavage, resulting in the release of massive FAM-DNA1 fragments from the AuNPs and the generation of fluorescent signal. This DNA walker based sensing strategy could detect PDGF-BB in a concentration range of 4 orders of magnitude with a detection limit down to sub-pM level. The practical applicability of the assay was demonstrated by detecting PDGF-BB secreted from MCF-7 cells with satisfactory results. The proposed DNA walker based assay could conveniently detect PDGF-BB with high sensitivity and good accuracy, along with the good extensibility of the assay, showing promise for practical diagnosis.
AuthorsHaiying Gan, Jie Wu, Huangxian Ju
JournalAnalytica chimica acta (Anal Chim Acta) Vol. 1074 Pg. 142-149 (Oct 03 2019) ISSN: 1873-4324 [Electronic] Netherlands
PMID31159934 (Publication Type: Journal Article)
CopyrightCopyright © 2019 Elsevier B.V. All rights reserved.
Chemical References
  • Aptamers, Nucleotide
  • Becaplermin
  • Gold
  • DNA
  • Thrombin
Topics
  • Aptamers, Nucleotide (chemistry, genetics)
  • Becaplermin (analysis)
  • Biological Assay (methods)
  • DNA (chemistry, genetics)
  • Gold (chemistry)
  • Humans
  • Limit of Detection
  • MCF-7 Cells
  • Metal Nanoparticles (chemistry)
  • Nucleic Acid Hybridization
  • Thrombin (analysis)

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