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Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization
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DNA Hybridization Measured with Graphene Transistor Arrays.

Kokoura Mensah1, Ismaïl Cissé1, Aurélie Pierret2

  • 1Laboratoire Nanobiophysique, ESPCI Paris, Université PSL, CNRS, Paris, 75005, France.

Advanced Healthcare Materials
|July 1, 2020
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Graphene field-effect transistors (GFETs) enable label-free DNA hybridization detection at femtomolar levels. This advancement utilizes protective coatings and electrostatic immobilization for sensitive and stable biosensing applications.

Keywords:
DNA hybridizationelectronic detectiongraphenereal-time hybridization measurementtransistor arrays

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A Microfluidic-based Electrochemical Biochip for Label-free DNA Hybridization Analysis
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Area of Science:

  • Nanotechnology
  • Biotechnology
  • Materials Science

Background:

  • Graphene field-effect transistors (GFETs) offer potential for label-free biosensing.
  • Existing methods for DNA detection often require complex labeling and can lack sensitivity.
  • Developing robust and biocompatible graphene-based devices is crucial for practical applications.

Purpose of the Study:

  • To fabricate high-quality graphene transistor arrays for sensitive DNA hybridization detection.
  • To develop a process for large-area graphene sheet fabrication with protective and biocompatible coatings.
  • To achieve label-free detection of DNA hybridization down to femtomolar concentrations.

Main Methods:

  • Fabrication of graphene field-effect transistor (GFET) arrays using chemical vapor deposition (CVD) grown graphene.
  • Development of protective Al2O3 and biocompatible SiOx capping layers for graphene sheets.
  • Electrostatic immobilization of DNA probes onto a poly-l-lysine coated chip surface.
  • Label-free detection of DNA hybridization using GFET arrays, including real-time in situ measurements.

Main Results:

  • High-quality GFET arrays with stable, near-zero Dirac point voltages were fabricated.
  • A detection limit of 10 femtomolar (fM) was achieved for 20-nucleotide DNA targets.
  • Stable measurements with minimal voltage drift (<1 mV/hour) and significant signal changes (~100 mV) were observed.

Conclusions:

  • The developed GFET fabrication process enables sensitive, label-free DNA hybridization detection.
  • The protective and biocompatible coatings ensure device stability and performance in biological environments.
  • This technology holds promise for advanced biosensing applications requiring high sensitivity and spatial resolution.