4.7 Article

An origami paper-based peptide nucleic acid device coupled with label-free DNAzyme probe hybridization chain reaction for prostate cancer molecular screening test

Journal

ANALYTICA CHIMICA ACTA
Volume 1186, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2021.339130

Keywords

Peptide nucleic acid; Paper-based analytical device; G-quadruplex; Prostate cancer; Molecular screening test; Hybridization chain reaction

Funding

  1. Thailand Research Fund (TRF)
  2. National Research Council of Thailand (NRCT) [PHD/0058/2560]
  3. Graduate School, Chulalongkorn University for the 90th Anniversary of Chulalongkorn University Fund (Ratchadaphiseksomphot Endowment Fund) [2563]

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A new PCA3 assay on an origami paper-based device was successfully developed in this study, allowing for molecular reactions and liquid control on the paper surface for quantitative detection of PCA3. The method was demonstrated to be effective for measuring PCA3 in urine matrix and human cancer cell lines, showing great potential for facile, rapid, and low-cost detection of PCA3 in real samples.
Prostate cancer associated 3 (PCA3) assay has been used to improve prostate cancer diagnosis and reduce unnecessary biopsies. In this work, we successfully developed a new PCA3 assay on an origami paper-based peptide nucleic acid device (oPAD). The PCA3 oPAD comprises an acrylic cassette and shutter slides to facilitate the molecular reaction and liquid control occurring on the paper surface. To quantify PCA3, a pyrrolidinyl peptide nucleic acid (acpcPNA) was immobilized onto the aldehyde-modified oPAD surface as a selective capture probe. A G-quadruplex (GQD) DNAzyme reporter probe was designed so that the PCA3 gene target binding triggered the hybridization chain reaction of the reporter probe, resulting in the accumulation of the GQD on the oPAD. The peroxidase activity of the GQD-hemin generated a deep green color of the oxidized ABTS substrate. Image analyses were performed in Adobe Photoshop CS6. The proposed oPAD was successfully applied in PCA3 detection ranges of 1-5 mu M (r(2) = 0.982) with a limit of detection of 0.5 mu M. Our proposed oPAD was demonstrated to measure PCA3 samples in both urine matrix and human cancer cell lines. The results reveal the great potential of our origami paper-based platform to be an alternative approach for facile, rapid, and low-cost detection of PCA3 in real samples. (C) 2021 Elsevier B.V. All rights reserved.

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