Micro-electrophoresis chip for moving and separating nucleic acids and other charged molecules

• US 6,261,430 B1
• Filed: 02/17/2000
• Issued: 07/17/2001
• Est. Priority Date: 06/08/1995
• Status: Expired due to Fees

• Current Assignee: Siemens Healthcare Diagnostics Incorporated (Siemens AG), Yoshiteru Sogawa
• Original Assignee: Visible Genetics, Inc. (Bayer AG)
• Inventors: Waterhouse, Paul, Stevens, John K., Larson, Marina T., Izmailov, Alexandre M., Yager, Thomas D., Maruzzo, Bruno C.
• Primary Examiner(s): Wallenhorst, Maureen M.
• Assistant Examiner(s): STARSIAK, JOHN S
• Application Number:
  US09/505,659
• Time in Patent Office: 516 Days
• Field of Search: 204/450, 204/451, 204/452, 204/453, 204/454, 204/455, 204/600, 204/601, 204/602, 204/603, 204/604, 204/605, 204/469
• US Class Current: 204/455
• CPC Class Codes: G01N 27/44704 Details; Accessories
• CPC Class Codes: G01N 27/44773 Multi-stage electrophoresis, e.g. two-dimensional electrophoresis
• CPC Class Codes: G01N 27/44791 Microapparatus sample containers with integrated microfluidic structures B01L3/5027

Abstract

A microelectrophoresis chip comprises a substrate in which there are formed one or more channels, one channel for each sample to be evaluated. The channels extend for the length of the chip, a distance of generally around 1 cm, and are about 1 to 10 μm wide and 1 to 10 μm in depth. The channels are filled with a homogeneous separation matrix which acts as an obstacle to the electrophoretic migration of the charged molecules. Microelectrodes disposed in the channels are used to induce an electric filed within the homogeneous separation medium. When a voltage is applied across two or more of the microelectrodes, the charged molecules are induced to move and separate according to the electric field density, the type of solvent film, and the charge, shape and size of the charged molecule. The chip may further comprise detectors, such as light polarization detectors, fluorescence emission detectors, biosensors, electrochemical sensors or other microcomponents which may include sites for enzymatic or chemical manipulation of the moved or separated charged molecules.

Claims

1. A microelectrophoresis chip comprising a substrate having formed therein at least one separation channel for performing separation formed on a first major surface, at least two electrodes disposed within the channel to induce an electric field within the channel, a homogeneous separation medium comprising water soluble fullerenes effective to act as obstacles to migration of biopolymers in a sample applied to the microelectrophoresis chip and in that the microelectrophoresis chip further comprises a detector element disposed on the chip for observation of migrating biopolymers.

2. The chip according to claim 1, wherein the separation channel is from 1 to 10 μ

m in depth.

3. The chip according to claim 1, wherein the chip has a plurality of separation channels.

4. The chip according to claim 3 wherein a plurality of anodes and a plurality of cathodes are disposed within each separation channel.

5. The chip according to claim 4, wherein the plurality of anodes and the plurality of cathodes are disposed to generate electric fields in at least two non-parallel directions.

6. A method for separating a mixture containing a plurality of species of biopolymers into subclasses of biopolymers comprising the steps of

(a) loading the mixture onto a chip for electrophoretic separation of charged polymers, said chip comprising a substrate having formed therein at least one separation channel for performing separation formed on a first major surface, at least two electrodes disposed within the channel to induce an electric field within the channel, a homogeneous separation medium comprising water soluble fullerenes effective to act as obstacles to migration of biopolymers in a sample applied to the microelectrophoresis chip and in that the microelectrophoresis chip further comprises a detector element disposed on the chip for observation of migrating biopolymers;

and

(b) applying an electric field to the chip to cause charged biopolymers in the mixture to migrate within the chip and be separated.

7. The method according to claim 6, further comprising the step of detecting the separated biopolymers within the chip.

8. The method according to claim 7, wherein the separated biopolymers are detected using a fluorescence detector.

9. A method for sequencing nucleic acids comprising the steps of

(a) loading a mixture containing products from a sequencing reaction onto a chip for electrophoretic separation of charged polymers, said chip comprising a substrate having formed therein at least one separation channel for performing separation formed on a first major surface, at least two electrodes disposed within the channel to induce an electric field within the channel, a homogeneous separation medium comprising water soluble fullerenes effective to act as obstacles to migration of biopolymers in a sample applied to the microelectrophoresis chip and in that the microelectrophoresis chip further comprises a detector element disposed on the chip for observation of migrating biopolymers,

(b) applying an electric field to the chip to cause charged biopolymers in the mixture to migrate within the chip;

and

(c) detecting separated bands of sequencing reaction products.

10. The method according to claim 9, wherein the separated bands are detected using a fluorescence detector.

11. An apparatus for separation of a plurality of species of biopolymers into subclasses of biopolymers comprising

(a) a holder for receiving a chip for electrohporetic separation of charged biopolymers,

(b) a microelectrophoresis chip comprising a substrate having formed therein at least one separation channel for performing separation formed on a first major surface, at least two electrodes disposed within the channel to induce an electric field within the channel, a homogeneous separation medium comprising water soluble fullerenes effective to act as obstacles to migration of biopolymers in a sample applied to the microelectrophoresis chip and wherein the microelectrophoresis chip further comprises a detector element disposed on the chip for observation of migrating biopolymers disposed with the holder.

12. The apparatus according to claim 11, wherein the detection element is part of a fluorescence detection system.

13. The apparatus according to claim 11, further comprising a loader for decreasing the volume of a sample to be loaded onto a chip disposed within the holder.

14. The apparatus according to claim 13, wherein the loader comprises a first concentration channel, a first pair of electrodes, a first semipermeable membrane effective to retain the biopolymers while allowing passage of smaller molecules, and a second pair of electrodes, wherein said first semipermeable membrane is located between the first pair of electrodes whereby biopolymers migrating in a first electric field generated within the first concentration channel between the first pair of electrodes are retained on the semipermeable membrane, and wherein the second pair of electrodes generate a second electric field perpendicular to the first electric field for migrating the retained biopolymers from the first semipermeable membrane.

15. The apparatus according to claim 14, further comprising a second concentration channel, a second semipermeable membrane effective to retain the biopolymers while allowing passage of smaller molecules, and a third pair of electrodes, said second pair of electrodes causing the retained biopolymers to migrate from the first semipermeable membrane through the second concentration channel to the second semipermeable membrane, and said third set of electrodes generating a third electric field perpendicular to the second electric field for migrating retained biopolymers from the second semipermeable membrane.

16. The apparatus according to claim 14, further comprising means for lowering the temperature in a portion of the first concentration channel to form a viscosity trap.

17. The apparatus according to claim 16, wherein the means for lowering the temperature in a portion of the first concentration channel is a thermocouple strip.