4.8 Article

Fluorescent paper-based DNA sensor using pyrrolidinyl peptide nucleic acids for hepatitis C virus detection

Journal

BIOSENSORS & BIOELECTRONICS
Volume 189, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2021.113381

Keywords

Fluorescent DNA sensor; Paper-based analytical device; Pyrrolidinyl peptide nucleic acid; Hepatitis C virus; Smartphone

Funding

  1. Second Century Fund (C2F), Chulalongkorn University
  2. Thailand Research Fund [RTA6280004]
  3. Center of Excellence on Petrochemical and Materials Technology (PETROMAT) through High Performance and Smart Materials (HPSM) research program
  4. National Research Council of Thailand (NRCT)
  5. Center of Excellence in Hepatitis and Liver Cancer, Department of Biochemistry, Faculty of Medicine, Chulalongkorn University

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A novel fluorescent paper-based DNA sensor using acpcPNA probe was developed for sensitive and selective detection of HCV. The sensor demonstrated great potential for clinical point-of-care applications, with successful application in clinical samples.
A novel fluorescent paper-based DNA sensor employing a highly specific pyrrolidinyl peptide nucleic acid (acpcPNA) probe was developed for the sensitive and selective detection of hepatitis C virus (HCV). The acpcPNA was covalently immobilized onto partially oxidized cellulose paper via reductive alkylation between the amine and the aldehyde groups. The fluorescence-based detection was performed by monitoring the fluorescence signal response of a fluorescent dye that selectively binds to the single-strand region of the DNA target over the PNA probe employing a custom-made portable fluorescent camera gadget in combination with a smartphone camera. Under the optimal conditions, a linear relationship between the fluorescence change in the green channel and the amount of HCV DNA from 5 to 100 pmol with a correlation coefficient of 0.9956, and the limit of detection of 5 pmol were obtained for short synthetic oligonucleotides. The acpcPNA probe exhibited very high selectivity for the complementary oligonucleotides over the single-base-mismatched, two-base-mismatched, and noncomplementary DNA targets. Benefitting from the signal amplification achieved through the numerous binding sites for the dye provided by the overhanging tail of long ssDNA target sequences, this system was successfully applied to detect the HCV complementary DNA (cDNA) obtained from clinical samples with satisfactory results. The proposed fluorescent paper-based sensor demonstrated a great potential to be used as a low-cost, simple, label-free, sensitive, and selective DNA sensor for point-of-care applications.

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