Ultra-rapid DNA sequencing method with nano-transistors array based devices

• US 20060246497A1
• Filed: 04/25/2006
• Published: 11/02/2006
• Est. Priority Date: 04/27/2005
• Status: Abandoned Application

• Current Assignee: Jung-Tang Huang
• Original Assignee: Jung-Tang Huang
• Inventors: Tsai, Cheng-Hung, Huang, Jung-Tang
• Application Number:
  US11/409,793
• Publication Number:
  US 20060246497A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: G01N 27/4145 specially adapted for biomolecules, e.g. gate electrode with immobilised receptors
• CPC Class Codes: G01N 27/4146 involving nanosized elements, e.g. nanotubes, nanowires

Abstract

The invention disclosed a method based on nano-transistors for ultra-rapid DNA sequencing. The method provides micro-fabricated electrodes, which are applied for stretching and driving DNA in the solution to overpass the fabricated carbon nanotube transistors (CNTFETs) array. When DNA molecules are moved perpendicularly to the axial direction of carbon nanotubes, the DNA molecule will touch carbon nanotube surface base after base such that it can measure current flow varied from different base according to charge transfer between the DNA molecule and the nanotubes. Due to this charge-transferred mechanism, the invention could achieve DNA sequencing and make a record or compare with the precedent in the database of DNA molecules.

Claims

1. An apparatus for rapid DNA sequencing, including at least one channel on a substrate, wherein each channel comprising:

a first cavity which can be dropped solution containing the single-stranded DNA molecules;

at least one nano-transistor comprising;

a semiconducting nanowire such as single-walled carbon nanotube;

a drain and source electrodes that said nanowire bridges on and can be

applied an AC voltage or low DC voltage;

and a back gate for the nano-transistor that can be applied a DC bias;

at least two pairs of electrodes perpendicular to the direction of DNA molecules transportation, set in front and back of the nano-transistor to be applied AC fields to stretch the DNA molecules before and after entering into the nano-transistor, and also can be applied positive DC bias on the electrodes to let the stretched DNA molecules arrive and pass the nano-transistor from said first cavity;

a set of measuring circuit connected to the nano-transistor that could measure the current variation while the bases pass through and contact with the nanowire;

a controller that could be applied for;

controlling the sign and magnitude of the DC bias, the amplitude and frequency of the AC fields;

conditioning the measured current signal of the nano-transistor into base sequences; and

recording or comparing said base sequences with the precedent in the database of DNA molecules.

2. The apparatus in claim 1 wherein said DC bias on the back gate of the nano-transistor could be negative to result in inducing positive charges distributed on the nanowire and the surface of the dielectric on the back gate such that the approaching DNA molecule is attracted to contact the nanowire.

3. The apparatus in claim 1 wherein said positive DC bias applied a larger amplitude of voltage on latter pair of electrodes used for stretching the DNA molecules, consequently, the DNA molecules with negative charges are attracted to the downstream of the channel through the nano-transistor, then the stretched DNA molecules can touch the surface of the nano-transistor.

4. The apparatus in claim 1 wherein said nano-transistor and measurement circuit could be installed more than two sets in a tandem arrangement such that the same DNA molecules could be sequenced several times, and the sequence data read by more than two nano-transistors would be cross-compared by the Bioinformatics technology to raise the accurate rate of the sequencing.

5. The apparatus in claim 1, further comprising DC bias electrodes which could be set on the right and left side of the DC stretching electrodes to confine the DNA molecules with negative charges in the middle area of the channel and be stretched straight easily.

6. The apparatus in claim 1, further comprising nanopore with 2-4 nm diameter which could be set in front or back of said first cavity so that the DNA molecule would be guided to pass through the nanopore by the electrophoresis and dielectrophoresis force in the solution, thereby only one DNA molecule would be driven into the nano-transistor measuring area at one time.

7. The apparatus in claim 1, further comprising two nonparallel electrodes could be set in front of and converge to said first cavity so that electrophoresis and dielectrophoresis force can be applied to guide the DNA to let only one DNA molecule to pass through the nanopore and be driven into the nano-transistor reading area at one time.

8. The apparatus in claim 1 wherein said nanowire has diameter less than 0.7 nm.

9. A method for rapid DNA sequencing with multi-channel is to apply multi-channel DNA sequencing apparatus containing at least one nano-transistor with a nano-wire, at least one set electrodes applied DC bias voltage, one set current measurement circuit and one controller, the method comprising:

(a) Dropping ion solution containing one or multiple kinds of DNA molecules on said channel;

(b) Applying DC/AC electric field on the electrodes to let the DNA molecules be stretched straight, driven through and contact with the nanowire of the nano-transistor;

(c) Measuring the current variation of the nano-transistor while the bases of DNA molecules pass through and contact the nanowire; and

(d) Conditioning and converting the measured current signal into the base sequences, which thereby being recorded or compared with the DNA molecule database further.