posted on 2015-11-25, 00:00authored byArun Richard Chandrasekaran, Johnny Zavala, Ken Halvorsen
Detection of nucleic acid sequences
is important for applications
such as medicine and forensics, but many detection strategies involve
multiple time-consuming steps or require expensive lab equipment.
Here we report a programmable DNA nanoswitch that undergoes a predefined
conformational change upon binding a target sequence, flipping the
switch from a linear “off” state to a looped “on”
state. The presence of the target sequence is determined without amplification
using standard gel electrophoresis to separate the on and off states.
We characterized the nanoswitch on a variety of DNA sequences and
fragment lengths, showing detection of fragments as short as 20-nt,
and sensitivity into the low picomolar range. Specificity and robustness
were demonstrated by detection of a single target sequence from both
a randomized pool of high concentration oligonucleotides and from
a solution of fetal bovine serum (FBS), with no false positive detection
in either case. Furthermore, we optimized the process to take less
than 30 minutes from sample mixture to readout. By leveraging the
already ubiquitous technique of gel electrophoresis, our low cost
approach will be especially accessible to researchers in the biomedical
sciences.