MIT Technology Review has details.
Several research groups are developing their own approach to nanopore sequencing. All involve the movement of DNA molecules through a tiny pore one base at a time; as the bases move through the pore, they can be read using various techniques. But one of the biggest obstacles to making a practical nanopore sequencer has been controlling the rate of the movement of the DNA. This is the problem the IBM group is working on. "The DNA goes through the pore too fast," says Gustavo Stolovitzky, manager of functional genomics and systems biology at IBM's T. J. Watson Research Center in Yorktown Heights, NY.
For the past two years, Stolovitzky's group at IBM has been developing chips arrayed with "DNA transistors" that use layered electrodes to control the movement of the DNA. The electrodes are built on the company's research fabrication line using the same technology employed to make silicon integrated circuits.
The IBM researchers first deposit conducting and semiconducting materials that will act as electrodes onto silicon wafer layers each about three nanometers thick. Then they use a transmission-electron microscope to blast a hole as small as one nanometer in diameter in the stack. A chip is cut from the wafer and placed in the middle of a container of potassium chloride, like a partition. DNA molecules are placed on one side of the solution, and a voltage is applied across the chip. Because DNA has an electrical charge, the IBM researchers can control its movement through the pore by using the electrodes to create electrical fields.
Controlling the movement of the DNA with microelectronics might prove more practical, and it seems to allow for better control, says Schloss.