Analytical methods and compositions

• US 20020164659A1
• Filed: 12/18/2001
• Published: 11/07/2002
• Est. Priority Date: 11/30/2000
• Status: Abandoned Application

• Current Assignee: Veridex LLC (Johnson & Johnson)
• Original Assignee: Veridex LLC (Johnson & Johnson)
• Inventors: Terstapper, Leon Wmm, Rao, Galla Chandra
• Application Number:
  US10/017,437
• Publication Number:
  US 20020164659A1
• Time in Patent Office: Days
• US Class Current: 435/7.5
• CPC Class Codes: C12Q 1/682 Signal amplification
• CPC Class Codes: C12Q 2537/143 Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
• CPC Class Codes: C12Q 2563/107 fluorescence
• CPC Class Codes: C12Q 2563/131 the label being a member of a cognate binding pair, i.e. extends to antibodies, haptens, avidin
• CPC Class Codes: C12Q 2563/143 Magnetism, e.g. magnetic label
• CPC Class Codes: G01N 2800/52 Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis
• CPC Class Codes: G01N 33/54313 the carrier being characterised by its particulate form
• CPC Class Codes: G01N 33/54326 Magnetic particles

Abstract

Compositions and analytical methods for detection of a single target entity or for simultaneous detection of multiple target entities by means of non-magnetic microparticles operably linked with a first binding partner capable of binding to a complementary second binding partner which, in turn, is operably linked to smaller magnetic particles to form a layer of magnetic particles on the non-magnetic microparticles.

Claims

1. A composition for the detection of one or more target entities in a mixture, said composition comprising non-magnetic microparticles or beads operably linked with a first binding partner capable of binding to a complementary second binding partner, said second binding partner being operably linked to magnetic particles smaller than the average size of said non-magnetic microparticles, thereby to form a layer of magnetic particles on said non-magnetic microparticles, wherein said magnetic particles bear variable amounts of free binding sites distal to the surface of said non-magnetic microparticles and wherein the bound magnetic particles are capable of binding both a labeled first binding partner and said first binding partner either in its free form or operably linked to one or more entities including entities for capturing said target entities in the mixture.

2. The composition of claim 1 wherein said non-magnetic microparticles are unlabeled.

3. The composition of claim 1 wherein said non-magnetic microparticles are detectably labeled.

4. The composition of claim 1 wherein said first binding partner is a biotin species.

5. The composition of claim 1 wherein said complementary second binding partner is an avidin species.

6. The composition of claim 1, wherein said free binding sites on said layer of magnetic particles are capable of directly or indirectly binding at least three additional entities.

7. The composition of claim 6 wherein said additional entities are selected from the group consisting of:

a) one or more target specific third binding partners operably linked to said first binding partner;

b) one or more detectable labels linked to first binding partner, c) a biotin species with affinity for blocking residual binding sites on the second binding partner located on the magnetic microparticles; and

d) one or more detectably labeled target specific fourth binding partners which are capable of binding one or more epitopes on bound target entities.

8. The composition of claim 7 wherein said third binding partner is an oligonucleotide probe operably linked to said first binding partner and wherein said probe is complementary to a target oligonucleotide sequence.

9. The composition of claim 7 wherein said third binding partner is an antibody.

10. The composition of claim 7 wherein said fourth binding partner is a target specific binder capable of recognizing epitopes on target entities different from those recognized by said third binding partner.

11. The composition of claim 7, wherein the detectable label is a fluorescent compound.

12. A method for the detection of one or more target entities in a mixture, which method comprises the steps of adding the composition of claim 1 to the mixture, incubating the mixture, separating the components of the mixture by magnetic means, and detecting one or more of the target entities in the mixture.

13. The method of claim 12, wherein said entities are selected from the group of particulate analytes and non-particulate analytes.

14. A kit for the detection of one or more target entities in a mixture, which kit comprises the composition of claim 1, an incubation means, a magnetic separation means, and a detection means.

16. The composition of claim 15, wherein the magnetic particles have an average size of less than 0.2 um.

17. The composition of claim 15, wherein the particles having a detectable fluorescent label have an average size of from about 1 to about 20 um.

15. A composition useful in the calibration of a diagnostic instrument system which utilizes fluorescent detection, said composition comprising magnetic particles bound to particles having a detectable fluorescent label, said magnetic particles having an average size less than that of the particles having a detectable fluorescent label.