Methods for manipulating moieties in microfluidic systems

• US 7,081,192 B1
• Filed: 08/10/2000
• Issued: 07/25/2006
• Est. Priority Date: 08/08/2000
• Status: Expired due to Term

• Current Assignee: AVIVA Biosciences Corporation
• Original Assignee: AVIVA Biosciences Corporation
• Inventors: Xu, Junquan, Wang, Xiaobo, Wu, Lei, Cheng, Jing, Yang, Weiping
• Primary Examiner(s): NOGUEROLA, ALEXANDER STEPHAN
• Application Number:
  US09/636,104
• Time in Patent Office: 2,175 Days
• Field of Search: 204/547, 204/643, 422/100, 422/50, 422/55, 422/68.1, 422/82.05, 422/101, 210/748, 435/4
• US Class Current: 204/547
• CPC Class Codes: B01L 2200/0647 Handling flowable solids, e.g. microscopic beads, cells, particles
• CPC Class Codes: B01L 2200/0668 Trapping microscopic beads
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2300/0864 comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
• CPC Class Codes: B01L 2400/0415 electrical forces, e.g. electrokinetic
• CPC Class Codes: B01L 2400/0424 Dielectrophoretic forces
• CPC Class Codes: B01L 2400/043 magnetic forces
• CPC Class Codes: B01L 2400/0436 acoustic forces, e.g. surface acoustic waves [SAW]
• CPC Class Codes: B01L 2400/0439 ultrasonic vibrations, vibrating piezo elements
• CPC Class Codes: B01L 2400/0454 radiation pressure, optical tweezers
• CPC Class Codes: B01L 2400/0496 Travelling waves, e.g. in combination with electrical or acoustic forces
• CPC Class Codes: B01L 3/502761 specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules investigating characteristics of particles G01N15/00
• CPC Class Codes: B03C 2201/26 for use in medical or biological applications
• CPC Class Codes: B03C 5/028 using travelling electric fields, i.e. travelling wave dielectrophoresis [TWD]
• CPC Class Codes: G01N 27/745 for detecting magnetic beads used in biochemical assays concerning the assays G01N33/54326; sensors therefor G01R33/1269; automatic analysers therefor G01N35/0098
• CPC Class Codes: G01N 33/54386 Analytical elements
• CPC Class Codes: G01N 33/569 for microorganisms, e.g. protozoa, bacteria, viruses

Abstract

This invention relates generally to the field of moiety or molecule manipulation in a chip format. In particular, the invention provides a method for manipulating a moiety in a microfluidic application, which method comprises: a) coupling a moiety to be manipulated onto surface of a binding partner of said moiety to form a moiety-binding partner complex; and b) manipulating said moiety-binding partner complex with a physical force in a chip format, wherein said manipulation is effected through a combination of a structure that is external to said chip and a structure that is built-in in said chip, thereby said moiety is manipulated.

Claims

1. A method for manipulating a moiety in a microfluidic application, which method comprises:

a) coupling a moiety to be manipulated onto a surface of a binding partner of said moiety to form a moiety-binding partner complex; and

b) manipulating said moiety-binding partner complex with a physical force in a microfluidic application chip format, wherein said manipulation is effected through a combination of a signal source that is external to said chip and a structure that is built into or on said chip, thereby said moiety is manipulated, and wherein said moiety is not directly manipulatable by an acoustic force and the moiety-binding partner complex is manipulated by an acoustic force.

2. The method of claim 1, wherein the moiety to be manipulated is selected from the group consisting of a cell, a cellular organelle, a virus, a molecule and an aggregate or complex thereof.

3. The method of claim 2, wherein the cell is selected from the group consisting of an animal cell a plant cell, a fungus cell, a bacterium cell and a recombinant cell.

4. The method of claim 2, wherein the cellular organelle is selected from the group consisting of a nuclei, a mitochondrion, a chloroplast, a ribosome, an ER, a Golgi apparatus, a lysosome, a proteasome, a secretory vesicle, a vacuole and a microsome.

5. The method of claim 2, wherein the molecule is selected from the group consisting of an inorganic molecule, an organic molecule and a complex thereof.

6. The method of claim 5, wherein the inorganic molecule is an ion selected from the group consisting of a sodium, a potassium, a magnesium, a calcium, a chlorine, an iron, a copper, a zinc, a manganese, a cobalt, an iodine, a molybdenum, a vanadium, a nickel, a chromium, a fluorine, a silicon, a tin, a boron and an arsenic ion.

7. The method of claim 5, wherein the organic molecule is selected from the group consisting of an amino acid, a peptide, a protein, a nucleoside, a nucleotide, an oligonucleotide, a nucleic acid, a vitamin, a monosaccharide, an oligosaccharide, a carbohydrate, a lipid and a complex thereof.

8. The method of claim 1, wherein the binding partner is a microparticle.

9. The method of claim 8, wherein the dimension of the microparticle is from about 0.01 micron to about several thousand microns.

10. The method of claim 8, wherein the microparticle is selected from the group consisting of a plastic particle, a polystyrene microbead, a glass bead, a magnetic bead, a hollow glass sphere, a metal particle, a particle of complex composition, and a microfabricated free-standing microstructure.

11. The method of claim 1, wherein the moiety is coupled to the surface of the binding partner directly or via a linker.

12. The method of claim 11, wherein the linker is a cleavable linker, and upon cleavage, the moiety is cleaved from the binding partner.

13. The method of claim 1, wherein the moiety is coupled to the surface of the binding partner via a covalent or a non-covalent linkage.

14. The method of claim 13, wherein the linkage between the moiety and the surface of the binding partner is effected via a specific or a non-specific binding.

15. The method of claim 13, wherein the linkage between the moiety and the surface of the binding partner is a cleavable linkage.

16. The method of claim 15, wherein the linkage is cleavable by a chemical, physical or an enzymatic treatment.

17. The method of claim 1, wherein the acoustic force is effected via a standing-wave acoustic field or a traveling-wave acoustic field.

18. The method of claim 1, wherein the acoustic force is effected via an acoustic field produced by piezoelectric material.

19. The method of claim 1, wherein the chip is selected from the group consisting of a silicon dioxide, a silicon nitride, a plastic, a glass, a ceramic, a photoresist and a rubber chip.

20. The method of claim 1, wherein the manipulation is selected from the group consisting of transportation, focusing, enrichment, concentration, aggregation, trapping, repulsion, levitation, separation, fractionation, isolation and linear or other directed motion of the moiety.

21. The method of claim 1, further comprising a step of decoupling the moiety from the surface of the binding partner after the moiety is manipulated.

22. The method of claim 1, wherein the moiety is a DNA, the binding partner is a porous bead and the DNA is reversibly absorbed onto the surface of the porous bead in a buffer containing high salt concentration.

23. The method of claim 1, wherein the moiety is a mRNA and the mRNA specifically binds to the surface of a binding partner that is modified to contain oligo-dT polynucleotide.

24. The method of claim 1, wherein the moiety is a protein and the protein non-specifically binds to the surface of a binding partner that is modified with a detergent.

25. The method of claim 24, wherein the detergent is SDS.

26. The method of claim 1, wherein the moiety is not directly manipulatable by a dielectrophoresis force and the moiety-binding partner complex is manipulated by a dielectrophoresis force.

27. The method of claim 1, wherein the moiety is not directly manipulatable by a traveling-wave dielectrophoresis force and the moiety-binding partner complex is manipulated by a traveling-wave dielectrophoresis force.

28. The method of claim 1, wherein the moiety is not directly manipulatable by an electrostatic force and the moiety-binding partner complex is manipulated by an electrostatic force.

29. The method of claim 1, wherein the moiety is not directly manipulatable by an optical radiation force and the moiety-binding partner complex is manipulated by an optical radiation force.

30. The method of claim 1, wherein at least 5% of the moiety to be manipulated is coupled onto surface of the binding partner.

31. The method of claim 1, wherein at least 90% of the moiety to be manipulated is coupled onto surface of the binding partner.

32. The method of claim 1, wherein a plurality of moieties is manipulated.

33. The method of claim 32, wherein the plurality of moieties is manipulated via a plurality of corresponding binding partners.

34. The method of claim 32, wherein the plurality of moieties is manipulated sequentially or simultaneously.

35. The method of claim 1, further comprising manipulating said moiety-binding partner complex by a physical force selected from the group consisting of a dielectrophoresis, a traveling-wave dielectrophoresis, a magnetic, an electrostatic, a mechanical, an optical radiation force and a thermal convection force.

36. The method of claim 35, wherein the dielectrophoresis force or the traveling wave dielectrophoresis is effected via electrical fields produced by electrodes.

37. The method of claim 35, wherein the magnetic force is effected via a magnetic field produced by a ferromagnetic material.

38. The method of claim 35, wherein the magnetic force is effected via a magnetic field produced by a microelectromagnetic unit.

39. The method of claim 35, wherein the electrostatic force is effected via a direct current (DC) electric field.

40. The method of claim 35, wherein the mechanical force is a fluidic flow force.

41. The method of claim 35, wherein the optical radiation force is effected via a laser tweezers.

42. The method of claim 1, wherein the moiety is a DNA and the DNA specifically binds to the surface of a binding partner via sequence specific hybridization or binding to an anti-DNA antibody.

43. The method of claim 1, wherein the moiety is a protein and the protein specifically binds to the surface of a binding partner that is modified with an antibody that specifically recognizes the protein.

44. The method of claim 1, wherein the moiety is not directly manipulatable by a magnetic force.

45. A kit for manipulating a moiety in a microfluidic application, which kit comprises:

a) a binding partner onto the surface of which a moiety to be manipulated can be coupled to form a moiety-binding partner complex;

b) means for coupling said moiety onto the surface of said binding partner; and

c) a chip on which said moiety-binding partner complex can be manipulated with a physical force that is effected through a combination of a signal source that is external to said chip and a structure that is built into or on said chip, and wherein said moiety is not directly manipulatable by an acoustic force and the moiety-binding partner complex is manipulated by an acoustic force.

46. The kit of claim 45, further comprising instruction(s) for coupling the moiety onto the surface of the binding partner and/or manipulating the moiety-binding partner complex on the chip.