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Low-Cost DNA Sequencing Technology a Step Closer to Reality

by Bidita Debnath on  November 24, 2014 at 11:07 PM Research News   - G J E 4
At Arizona State University's Biodesign Institute and IBM's T.J. Watson Research Center, a team of scientists have developed a prototype DNA reader that could make whole genome profiling an everyday practice in medicine.
 Low-Cost DNA Sequencing Technology a Step Closer to Reality
Low-Cost DNA Sequencing Technology a Step Closer to Reality
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"Our goal is to put cheap, simple and powerful DNA and protein diagnostic devices into every single doctor's office," said Stuart Lindsay, an ASU physics professor and director of Biodesign's Center for Single Molecule Biophysics. Such technology could help usher in the age of personalized medicine, where information from an individual's complete DNA and protein profiles could be used to design treatments specific to their individual makeup.

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Such game-changing technology is needed to make genome sequencing a reality. The current hurdle is to do so for less than $1,000, an amount for which insurance companies are more likely to provide reimbursement.

In their latest research breakthrough, the team fashioned a tiny, DNA reading device a thousands of times smaller than width of a single human hair.

The device is sensitive enough to distinguish the individual chemical bases of DNA (known by their abbreviated letters of A, C, T or G) when they are pumped past the reading head.

Proof-of-concept was demonstrated, by using solutions of the individual DNA bases, which gave clear signals sensitive enough to detect tiny amounts of DNA (nanomolar concentrations), even better than today's state-of-the-art, so called next-generation DNA sequencing technology.

Making the solid-state device is just like making a sandwich, just with ultra high-tech semiconductor tools used to slice and stack the atomic-sized layers of meats and cheeses like the butcher shop's block. The secret is to make slice and stack the layers just so, to turn the chemical information of the DNA into a change in the electrical signal.

First, they made a "sandwich" composed of two metal electrodes separated by a two-nanometer thick insulating layer (a single nanometer is 10,000 times smaller than a human hair), made by using a semiconductor technology called atomic layer deposition.

Then a hole is cut through the sandwich: DNA bases inside the hole are read as they pass the gap between the metal layers.

"The technology we've developed might just be the first big step in building a single-molecule sequencing device based on ordinary computer chip technology," said Lindsay.

"Previous attempts to make tunnel junctions for reading DNA had one electrode facing another across a small gap between the electrodes, and the gaps had to be adjusted by hand. This made it impossible to use computer chip manufacturing methods to make devices," said Lindsay.

"Our approach of defining the gap using a thin layer of dielectric (insulating) material between the electrodes and exposing this gap by drilling a hole through the layers is much easier," he said. "What is more, the recognition tunneling technology we have developed allows us to make a relatively large gap (of two nanometers) compared to the much smaller gaps required previously for tunnel current read-out (which were less than a single nanometer wide). The ability to use larger gaps for tunneling makes the manufacture of the device much easier and gives DNA molecules room to pass the electrodes."

Specifically, when a current is passed through the nanopore, as the DNA passes through, it causes a spike in the current unique to each chemical base (A, C, T or G) within the DNA molecule. A few more modifications are made to polish and finish the device manufacturing.

The team encountered considerable device-to-device variation, so calibration will be needed to make the technology more robust. And the final big step - of reducing the diameter of the hole through the device to that of a single DNA molecule - has yet to be taken.

Source: Eurekalert
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