4.7 Article

Consumer electronics devices for DNA genotyping based on loop-mediated isothermal amplification and array hybridisation

Journal

TALANTA
Volume 198, Issue -, Pages 424-431

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2019.01.124

Keywords

Single-nucleotide polymorphism; Isothermal DNA amplification; Point-of-care testing; Smartphone; Scanner; Compact disc

Funding

  1. Generalitat Valenciana, Spain [GVA-PROMETEOII/2014/040, GRISOLIA/2014/024]
  2. Spanish Ministry of Economy and Competitiveness, Spain by U. E. FEDER funds [MINECO CTQ2016-75749-R]

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Consumer electronic technologies offer practical performances to develop compact biosensing systems intended for the point-of-care testing of DNA biomarkers. Herein a discrimination method for detecting single nucleotide polymorphisms, based on isothermal amplification and on-chip hybridisation, was developed and integrated into user-friendly optical devices: e.g., USB digital microscope, flatbed scanner, smartphone and DVD drive. In order to adequately identify a single base change, loop-mediated isothermal amplification (LAMP) was employed, with high yields (8 orders) within 45 min. Subsequently, products were directly hybridised to the allele-specific probes attached to plastic chips in an array format. After colorimetric staining, four consumer electronic techniques were compared. Sensitive precise measurements were taken (high signal-to-noise ratios, 10-mu m image resolution, 99% scan-to-scan reproducibility). These features confirmed their potential as analytical tools, are a competitive alternative to fluorescence scanners, and incorporate additional advantages, such as user-friendly interface and connectivity for telemedicine needs. The analytical performances of the integrated platform (assay and reader) in the human samples were also excellent, with a low detection limit (100 genomic DNA copies), and reproducible (< 15%) and cheap assays (< 10 (sic)/test). The correct genotyping of a genetic biomarker (single-nucleotide polymorphism located in the GRIK4 gene) was achieved as the assigned genotypes agreed with those determined by using sequencing. The portability, favourable discriminating and read-out capabilities reveal that the implementation of mass-produced low-cost devices into minimal-specialised clinical laboratories is closer to becoming a reality.

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