An ion-exchange nanomembrane sensor for detection of nucleic acids using a surface charge inversion phenomenon.

Biosens Bioelectron

Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, IN 46556, USA; Advanced Diagnostics & Therapeutics, University of Notre Dame, Notre Dame, IN 46556, USA; Harper Cancer Research Institute, University of Notre Dame, Notre Dame, IN 46556, USA. Electronic address:

Published: October 2014

AI Article Synopsis

  • The study introduces an innovative and affordable biosensor designed for quick and accurate detection of nucleic acids using an ionic diode formed by anion exchange nanoporous membranes.
  • The sensor works by detecting changes in ion conductance when negatively charged nucleic acids hybridize with functionalized probes on its surface, allowing it to identify even minor genetic variations related to diseases like oral cancer and dengue virus.
  • It demonstrates a low detection limit of 1 pM for target molecules in a fast 15-minute assay, making it suitable for practical applications in food safety, medical diagnostics, and environmental monitoring.

Article Abstract

We present a novel low-cost biosensor for rapid, sensitive and selective detection of nucleic acids based on an ionic diode feature of an anion exchange nanoporous membrane under DC bias. The ionic diode feature is associated with external surface charge inversion on the positively charged anion exchange nanomembrane upon hybridization of negatively charged nucleic acid molecules to single-stranded oligoprobes functionalized on the membrane surface resulting in the formation of a cation selective monolayer. The resulting bipolar membrane causes a transition from electroconvection-controlled to water-splitting controlled ion conductance, with a large ion current signature that can be used to accurately quantify the hybridized nucleic acids. The platform is capable of distinguishing two base-pair mismatches in a 22-base pairing segment of microRNAs associated with oral cancer, as well as serotype-specific detection of dengue virus. We also show the sensor' capability to selectively capture target nucleic acids from a heterogeneous mixture. The limit of detection is 1 pM for short 27 base target molecules in a 15-min assay. Similar hybridization results are shown for short DNA molecules as well as RNAs from Brucella and Escherichia coli. The versatility and simplicity of this low-cost biosensor should enable point-of-care diagnostics in food, medical and environmental safety markets.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445831PMC
http://dx.doi.org/10.1016/j.bios.2014.04.008DOI Listing

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