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  2. Peptide-Fluorophore Hydrogel as a Signal Boosting Approach in Rapid Detection of Cancer DNA

Peptide-Fluorophore Hydrogel as a Signal Boosting Approach in Rapid Detection of Cancer DNA

  • ACS Omega. 2019 Aug 16;4(9):13889-13895. doi: 10.1021/acsomega.9b01586.
Bernhard Jandl 1 2 Sima Sedghiniya 1 3 Annika Carstens 1 4 Kira Astakhova 1
Affiliations

Affiliations

  • 1 Department of Chemistry, Technical University of Denmark, 206-207 Kemitorvet, 2800 Kgs Lyngby, Denmark.
  • 2 Institute of Applied Synthetic Chemistry, TU Wien (Vienna University of Technology), Getreidemarkt 9, 1060 Wien, Austria.
  • 3 School of Chemistry, College of Science, University of Tehran, Tehran 14155-6455, Iran.
  • 4 Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, Campusvej 55, 5230 Odense M, Denmark.
Abstract

Cancer is a major health risk in the modern society that requires rapid, reliable, and inexpensive diagnostics. Because of the low abundance of Cancer DNA in biofluids, current detection methods require DNA amplification. The amplification can be challenging; it provides only relative quantification and extends time and cost of an assay. Herein, we report a new oligonucleotide hybridization platform for amplification-free detection of human Cancer DNA. Using a large PEG-capture probe allows rapid separation of the bound (mutant) versus unbound (wild type) DNA. Next, a supramolecular hydrogel forming peptide attached to a detection oligonucleotide probe serves as a signal amplification tool. Having screened multiple short Peptides and fluorophores, we identified the system P1 + cyanine 3.5 that allows for sensitive quantitative detection of mutation L858R in EGFR oncogene. The peptide-fluorophore-based assay provides absolute target DNA quantification at the detection limit of 20 ng Cancer DNA versus >500 ng for Cy3.5-labeled oligonucleotide in only 1 hour.

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