Assay involving detection and identification with encoded particles

• US 7,291,504 B2
• Filed: 03/10/2003
• Issued: 11/06/2007
• Est. Priority Date: 04/25/1996
• Status: Expired due to Fees

• Current Assignee: BioArray Solutions Limited (Werfen SA)
• Original Assignee: BioArray Solutions Limited (Werfen SA)
• Inventors: Seul, Michael
• Primary Examiner(s): Le; Long V.
• Assistant Examiner(s): Yu; Melanie J.
• Application Number:
  US10/385,012
• Publication Number:
  US 20040096846A1
• Time in Patent Office: 1,702 Days
• Field of Search: 435/6, 435/7.1, 435/7.4, 435 792- 794, 435/174, 435/287.2, 435/287.9, 435/288.7, 435/287.3, 436/501, 436/518, 436/536, 436/56, 436/63, 436/164, 436/800
• US Class Current: 436/518
• CPC Class Codes: B01J 19/0046 Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays synthesis methods per se C40B50/00
• CPC Class Codes: B01J 2219/00432 Photolithographic masks
• CPC Class Codes: B01J 2219/00448 using microlens arrays
• CPC Class Codes: B01J 2219/00468 by manipulation of individual beads
• CPC Class Codes: B01J 2219/005 Beads
• CPC Class Codes: B01J 2219/00527 Sheets
• CPC Class Codes: B01J 2219/00585 Parallel processes
• CPC Class Codes: B01J 2219/00596 Solid-phase processes
• CPC Class Codes: B01J 2219/00648 by the use of solid beads
• CPC Class Codes: B01J 2219/00653 the compounds being bound to electrodes embedded in or on the solid supports
• CPC Class Codes: B01J 2219/00659 Two-dimensional arrays
• CPC Class Codes: B01J 2219/00677 Ex-situ synthesis followed by deposition on the substrate
• CPC Class Codes: B01J 2219/00722 Nucleotides
• CPC Class Codes: B01J 2219/00725 Peptides
• CPC Class Codes: B01J 2219/00743 Cells
• CPC Class Codes: C12Q 1/6825 Nucleic acid detection involving sensors
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 2563/155 Particles of a defined size, e.g. nanoparticles
• CPC Class Codes: C12Q 2565/501 being an array of oligonucleotides
• CPC Class Codes: C12Q 2565/607 being a sensor, e.g. electrode
• CPC Class Codes: C40B 50/18 : using a particular method of attachment to the solid support
• CPC Class Codes: C40B 60/14 : for creating libraries

Abstract

A method and apparatus for the manipulation of colloidal particles and biomolecules at the interface between an insulating electrode such as silicon oxide and an electrolyte solution. Light-controlled electrokinetic assembly of particles near surfaces relies on the combination of three functional elements: the AC electric field-induced assembly of planar aggregates; the patterning of the electrolyte/silicon oxide/silicon interface to exert spatial control over the assembly process; and the real-time control of the assembly process via external illumination. The present invention provides a set of fundamental operations enabling interactive control over the creation and placement of planar arrays of several types of particles and biomolecules and the manipulation of array shape and size. The present invention enables sample preparation and handling for diagnostic assays and biochemical analysis in an array format, and the functional integration of these operations. In addition, the present invention provides a procedure for the creation of material surfaces with desired properties and for the fabrication of surface-mounted optical components.

Claims

1. An assay method comprising:

(i) providing a planar array of particles randomly-positioned with respect to particle type, where different types of particles are differently encoded by incorporation of an optically detectable characteristic into the particles that permits said differently encoded particles to be distinguished, and wherein said differently encoded particles have different binding molecules attached thereto;

(ii) determining the spatial coordinates of particular particle types within the planar array;

(iii) contacting said array of particles with a solution such that, if a particular type of analyte is present in said solution, said analyte binds to the corresponding binding molecules of said particles and the binding of said analyte is indicated by an optically detectable signal;

(iv) determining the presence of any such bound analyte by determining the presence of said optically detectable signal; and

(v) identifying said optically detectable characteristic of particles having binding molecules bound to an analyte, without moving or separating said particles being interrogated from other particles in the array, by correlating the spatial coordinates of said particles with the location of the optically detectable signals in order to identify said binding molecules bound to an analyte.

2. The medthod of claim 1, wherein the step of identifying the optically detectable characteristic of the particles types is performed before the step of contacting said array.

3. The method of claim 1, wherein the step of identifying the optically detectable characteristic of the particles types is performed after the step of contacting said array.

4. The method of performing an assay according to claim 1, wherein the analyte and binding molecule form a binding pair, wherein one member of the pair is a receptors and the other member is a ligand, one member is an antibody and the other member is an antigen, or one member is an enzyme and the other member is a substrate.

5. The method of performing an assay according to claim 1, wherein the analyte and binding molecule form a binding pair, wherein the members of the pair are complementary nucleic acid strands.

6. The method of claim 5, wherein one of the nucleic acid strands is cDNA and the complementary strands is an oligonucleotide probe, and wherein the method comprises the step of detecting hybridization between the cDNA and the oligonucleotide probe.

7. Then method of claim 6, wherein the cDNA is labeled.

8. The method of claim 5, wherein one of the nucleic acid strands is produced by PCR amplification and the complementary strands is an oligonucleotide probe, and wherein the method comprises the step of detecting hybridization between the nucleic acid strand and the oligonucleotide probe.

9. The method of claim 1, wherein said analyte binding molecule is an enzyme and wherein the assay comprises the steps of reacting the enzyme with a target analyte in the solution and detecting enzyme reaction products that are released into the solution.

10. The method of claim 1, wherein optically detectable characteristic is color.

11. The method of claim 1, wherein the solution comprises fluorescently labeled analytes, and the step of determining the presence of bound analyte comprises recording fluorescence from individual particles within the array of particles to determine the quantity of one or more associated analytes.

12. The method of claim 1, wherein the step of contacting said array of particles comprises contacting tie array of particles with a solution comprising a fluorescently labeled first analyte, such that said first analyte is capable of binding to a corresponding first binding molecule to form a fluorescent first paired entity, the method further comprising the steps of detecting the fluorescence of the array of particles subsequent to the formation of the first paired entity;

contacting said array of particles with a non-fluorescent second analyte at increasing concentrations, wherein the non-fluorescent second analyte has a known binding constant and can bind to the first binding molecule, displacing the fluorescently labeled first analyte from the first paired entity to form a second paired entity; and

detecting the change in fluorescence of the array of particles as a function of the concentration of the non-fluorescent second analyte.

13. The method of claim 1, wherein the step of contacting said array of particles comprises contacting said array of particles with a solution comprising a first analyte, such that said first analyte is capable of forming a first paired entity with a corresponding binding molecule, the method further comprising the step of contacting said array of particles, subsequent to the step of contacting said array of particles, with another solution comprising a second analyte, different from the first analyte, said second analyte capable of forming a second paired entity.

14. The method of claim 13, wherein the second paired entity is formed by the binding of the second analyte with the first paired entity, and wherein the second analyte is fluorescently colored.

15. The method of claim 14, wherein the second paired entity is formed by displacing the first analyte in the first paired entity with the second analyte.

16. The method of claim 13, wherein the first analyte and the second analyte bind to different binding molecules.

17. The method of claim 1, wherein said array of particles is chemically anchored to the substrate.

18. The method of claim 1, wherein the step of providing a planar array further comprises providing a multiplicity of said planar arrays on said substrate, wherein the location of each array on said substrate indicates the encoded particles located therein.

23. The method of claim 1 or 19 wherein the planar array of particles are arranged on a defined area of the substrate surface.

24. The method of claim 1 or 19 wherein the planar array of particles are permanently anchored to said substrate.

19. A method of performing an assay using at least one planar array of particles, the method comprising:

forming the planar array with a number of differently encoded particles, on a defined area of a substrate but wherein differently-encoded particles are randomly-positioned within said area, said differently encoded particles having different analyte binding molecules attached thereto, said particle types being encoded by incorporation of an optically detectable characteristic into the particles, that distinguishes said differently encoded particles and the binding molecules attached thereto;

determining the spatial coordinates of particular particle types within the planar array;

contacting said plurality of particles with a solution such that, if particular analytes are present in said solution, said analytes bind to the corresponding binding molecules attached to said particles to form a paired entity and said analytes carry an optically detectable characteristic;

detecting said paired entities; and

identifying, the optically detectable characteristic of the particles to which binding molecules are attached which form paired entities by correlating the spatial coordinates of said particles with the spatial coordinates of he optically detectable characteristic in order to identify said binding molecules forming said paired entities.

20. The method of claim 19, further comprising the step of selectively marking at least one individual particle within the array of particles.

21. The method of claim 20, wherein the step of marking comprises using a focused beam of light to initiate a photochemical color-reaction.

22. The method of claim 19, further comprising:

forming a layer of a plurality of molecules of a single distinct type on the substrate, prior to forming the array of particles, the molecules capable of retaining particles with a desired characteristic, and disassembling the array of particles selectively to form a set of retained particles wherein at least one type of molecule associated with the set of retained particles has a chemical or biochemical affinity for the molecules on the substrate.