A microfluidic platform for transcription- and amplification-free detection of zepto-mole amounts of nucleic acid molecules

Biosens Bioelectron. 2016 Apr 15:78:1-6. doi: 10.1016/j.bios.2015.11.013. Epub 2015 Nov 10.

Abstract

Here we report the development of a device for the transcription- and amplification-free detection of DNA and RNA molecules down to the zepto-mole range. A microfluidic chip with a built-in microarray was used for manipulation of nano-liter sample volumes. Specific staining and immobilization of the target molecules was achieved via a double hybridization approach thereby avoiding bias due to enzymatic processes like reverse transcription and PCR amplification. Therefore, target molecules were indirectly labeled by pre-hybridization to complementary Cy5-labeled probes. The remaining single-stranded portion of each target molecule could subsequently hybridize to complementary capture probes of a microarray. Thus a target-mediated immobilization of labeled DNA took place. By means of an ultra-sensitive fluorescence readout, all molecules hybridized to the microarray could be detected. The combination of minimized sample volume and single molecule detection yielded a detection limit of 39 fM (831 molecules in 35.4 nl assay volume) for target DNA and 16 fM (338 molecules) for target RNA after 1h on-chip hybridization.

Keywords: DNA; Lab-on-a-chip; Microarray; Microfluidic biochip; RNA; Ultra-sensitive detection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques / methods*
  • DNA / genetics
  • DNA / isolation & purification*
  • Fluorescence
  • Limit of Detection
  • Microfluidics / methods*
  • Nucleic Acid Amplification Techniques / methods
  • Nucleic Acid Hybridization / methods
  • Oligonucleotide Array Sequence Analysis / methods
  • RNA / genetics
  • RNA / isolation & purification*
  • Transcription, Genetic*

Substances

  • RNA
  • DNA