Here is the abstract you requested from the imaps_2018 technical program page. This is the original abstract submitted by the author. Any changes to the technical content of the final manuscript published by IMAPS or the presentation that is given during the event is done by the author, not IMAPS.
|Sequence-Specific Nucleic Acid Detection at 1 aM; Microfluidics Device|
|Keywords: RNA detection, Pathogen detection, PCR-free diagnostics|
|A PCR-free, optics-free platform has been developed for the detection of bacterial 16S rRNA at 1 aM (10- 18 M). This sequence-specific nucleic acid (NA) detector is based on electromechanical signal transduction using a nanopore-based scheme. Our microfluidics device utilizes peptide nucleic acid (PNA) capture probes conjugated to polystyrene beads. Since PNA is charge neutral, the bead-PNA conjugates may be designed to be 'charge neutral' until they hybridize target NA, at which point the complex becomes negatively charged and mobile in an electric field. If the electric field is oriented through a pore that is too small for the bead-PNA conjugate with hybridized target to pass through, it will block the pore thereby causing an easily measured step reduction in ionic current. In this way, the selective, NA hybridization event is electromechanically transduced. This device has proven capable of detecting E. coli 16S rRNA at 1 aM against a 1 pM background of RNA from Pseudomonas putida and shows promise for integration into portable, low-cost systems for rapid detection of pathogenic bacteria in body fluids, food, and water. This presentation will provide insight into these detection mechanisms, the configuration and construction of the microfluidics and microelectronics interfacing, and strategies for device scale-up to larger production volumes.|
|Harold G. Monbouquette, Professor
University of California, Los Angeles
Los Angeles, CA