Multi-mode separation for target detection

• US 9,797,817 B2
• Filed: 05/03/2013
• Issued: 10/24/2017
• Est. Priority Date: 05/03/2012
• Status: Active Grant

• Current Assignee: Board of Regents of the University of Michigan (University of Michigan)
• Original Assignee: Board of Regents of the University of Michigan (University of Michigan)
• Inventors: McNaughton, Brandon H., Kinnunen, Paivo, Younger, John G.
• Primary Examiner(s): Chin, Chris L
• Application Number:
  US13/887,264
• Publication Number:
  US 20130337455A1
• Time in Patent Office: 1,635 Days
• Field of Search: 436526
• CPC Class Codes: B03C 1/01 by addition of magnetic adjuvants
• CPC Class Codes: B03C 1/288 disposed at the outer circumference of a recipient
• CPC Class Codes: B03C 2201/18 Magnetic separation whereby the particles are suspended in a liquid
• CPC Class Codes: B03C 2201/26 for use in medical applications
• CPC Class Codes: C12Q 1/6804 Nucleic acid analysis using immunogens immunoassay G01N33/53
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 2563/143 Magnetism, e.g. magnetic label
• CPC Class Codes: C12Q 2563/149 Particles, e.g. beads
• CPC Class Codes: C12Q 2565/101 Interaction between at least two labels
• CPC Class Codes: G01N 1/30 Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis
• CPC Class Codes: G01N 33/54326 Magnetic particles
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing

Abstract

Sandwich separation is based on forming a sandwich complex with a magnetic bead, buoyant bead, and a target. Once a sandwich formation is created, the sandwich can be separated using its dual physical properties, namely magnetism and buoyancy. Sandwich separation is highly specific, allows for removal of the beads that do not have any attached target, and reduces the number of background beads. Sandwich separation can also be used to allow for target detection in raw specimen. Also, improvement of detection capability is accomplished by performing AMBR measurements on a solid interface, where the rotational period speeds up and allows for dramatically reduced time-to-result.

Claims

1. A method of forming, manipulating and isolating a sandwich complex, wherein the complex consists of one or more magnetic beads, one or more buoyant beads, and a target analyte, and where the one or more buoyant beads in the complex provide sufficient buoyancy such that the complex floats, the method comprising:

(a) contacting the sample in a solution with (i) a population of the one or more magnetic beads, each magnetic bead comprising a moiety that can specifically associate with the target analyte under appropriate conditions and (ii) a population of the one or more buoyant beads, each buoyant bead comprising a moiety that can specifically associate with the target analyte under appropriate conditions, wherein contact results in formation of the complex containing the one or more magnetic beads, the one or more buoyant beads, and the target analyte, such that the complex is both magnetic and buoyant; and

(b) isolating the complex based on the combined movement of the complex in a magnetic field and in a gravitational or centrifugal field.

2. The method of claim 1 wherein the magnetic bead moiety and the buoyant bead moiety are different.

3. The method of claim 1, wherein the magnetic bead and the buoyant bead are added to the sample sequentially.

4. The method of claim 1, wherein the magnetic bead is added prior to addition of the buoyant bead.

5. The method of claim 1, wherein the magnetic bead moiety and/or the buoyant bead moiety is selected from the group consisting of a protein, a charge and a nucleic acid.

6. The method of claim 5 wherein the protein is an antibody.

7. The method of claim 1, wherein the target is selected from the group consisting of a cell, a protein, a nucleic acid and a small molecule.

8. The method of claim 7 wherein the cell is a eukaryotic cell.

9. The method of claim 7 wherein the cell is a prokaryotic cell.

10. The method of claim 1, wherein the magnetic bead and/or the buoyant bead are removed following isolation of the target.

11. The method of claim 1, wherein the magnetic bead moiety and/or the buoyant bead moiety comprises a detectable label.

12. The method of claim 1 further comprising removing the magnetic bead and/or the buoyant bead that is not associated with the target from the sample.

13. The method of claim 1 further comprising removing the magnetic bead and/or the buoyant bead that is associated with the target from the sample.

14. The method of claim 1 further comprising an additional buoyant bead comprising a moiety that can specifically associate with a target, wherein the buoyant bead and the additional buoyant bead have different buoyancies relative to each other.

15. The method of claim 1, wherein the movement in the magnetic field and the gravitational or centrifugal field are performed simultaneously.

16. The method of claim 1, wherein the movement in the magnetic field and the gravitational or centrifugal field are performed separately.

17. The method of claim 16, wherein the complex is subjected to the magnetic field prior to being subjected to the gravitational or centrifugal field.