ULTRA-SENSITIVE DETECTION OF ENZYMES BY CAPTURE-AND-RELEASE FOLLOWED BY QUANTIFICATION

• US 20100075355A1
• Filed: 09/23/2008
• Published: 03/25/2010
• Est. Priority Date: 09/23/2008
• Status: Abandoned Application

• Current Assignee: Quanterix Corporation
• Original Assignee: Quanterix Corporation
• Inventors: Randall, Jeffrey D., Walt, David R., Duffy, David C., Rissin, David M., Ferrell, Evan
• Application Number:
  US12/236,490
• Publication Number:
  US 20100075355A1
• Time in Patent Office: Days
• US Class Current: 435/18
• CPC Class Codes: G01N 33/543 with an insoluble carrier for immobilising immunochemicals
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms
• CPC Class Codes: G01N 33/54393 Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding

Abstract

The present invention relates to systems and methods for detecting analyte molecules or particles in a fluid sample and in some cases, determining a measure of the concentration of the molecules or particles in the fluid sample. Methods of the present invention may comprise immobilizing a plurality of analyte molecules or particles to form a plurality of complexes, releasing at least a portion of some of the plurality of complexes, determining at least a portion of the plurality of complexes released, and determining a measure of the concentration of the analyte molecules or particles in a fluid sample.

Claims

1. A method of detecting analyte molecules or particles in a fluid sample, comprising:

exposing a substrate comprising a plurality of capture components to a sample comprising a plurality of analyte molecules or particles, so that analyte molecules or particles associate with capture components to form a plurality of complexes, each complex being immobilized with respect to the substrate and comprising at least one capture component, at least one analyte molecule or particle, and at least one enzymatic component;

exposing the substrate to a dissociating agent, which has essentially no specific affinity for the capture components, to cause at least a portion of at least some of the plurality of complexes to dissociate from the substrate to form a plurality of dissociated species, which are not immobilized with respect to the substrate and wherein at least some of the dissociated species each comprise at least a portion of the enzymatic component; and

determining the presence of and/or a measurement of the amount or concentration of the analyte molecules or particles in the fluid sample based at least in part on detecting a least some of the dissociated species.

2. The method of claim 1, wherein the enzymatic component is beta-galactosidase.

3. The method of claim 1, wherein the enzymatic component is horse-radish peroxidase.

4. The method of claim 1, wherein the dissociating agent comprises at least one of a pH agent, a salt agent, a denaturing agent, a reducing agent, a chemical agent, and an enzyme.

5. The method of claim 1, wherein the dissociating agent comprises beta-mercaptoethanol.

6. The method of claim 1, wherein the dissociating agent comprises dithiothreitol.

7. The method of claim 1, wherein at least some of the dissociated species are detected by partitioning the dissociated species across a plurality of reaction vessels.

8. The method of claim 7, wherein the plurality of dissociated species are partitioned such that a statistically significant fraction of the reaction vessels contain no dissociated species and a statistically significant fraction of reaction vessels contain at least one dissociated species.

9. The method of claim 7, wherein the plurality of dissociated species are partitioned such that a statistically significant fraction of the reaction vessels contain no dissociated species and a statistically significant fraction of reaction vessels contain one dissociated species.

10. The method of claim 7, further comprising determining the number of the reaction vessels and/or fraction of the reaction vessels that contain or do not contain a dissociated species

11. The method of claim 10, wherein the number or fraction of the reaction vessels that contain a dissociated species is used to determine a measure of the concentration of analyte molecules or particles in the fluid sample.

12. The method of claim 10, wherein the number or fraction of the reaction vessels that contain a dissociated species is directly proportional to the concentration of analyte molecules or particles in the sample.

13. The method of claim 10, wherein the number or fraction of the reaction vessels that contain a dissociated species is less than the number of analyte molecules or particles contained in a volume of the sample applied to the substrate in the exposing act.

14. The method of claim 1, wherein the substrate comprises a plurality of beads.

15. The method of claim 14, wherein the beads are magnetic.

16. The method of claim 1, wherein the substrate comprises a microtiter plate.

17. The method of claim 7, wherein the plurality of reaction vessels is formed on the end of a fiber optic bundle.

18. The method of claim 7, wherein the plurality of reaction vessels are formed upon the mating of at least a portion of a sealing component and at least a portion of a second substrate.

19-50. -50. (canceled)

51. A method for determining a measure of the concentration of analyte molecules or particles in a fluid sample, comprising:

exposing a substrate comprising a plurality of capture components to a sample comprising a plurality of analyte molecules or particles, so that analyte molecules or particles associate with capture components to form a plurality of complexes, each complex being immobilized with respect to the substrate and comprising at least one capture component and at least one analyte molecule or particle;

exposing the plurality of complexes to a plurality of binding ligands comprising an enzymatic component, wherein at least one binding ligand is immobilized with respect to at least some of the complexes;

exposing the plurality of complexes to a dissociating agent, which has essentially no specific affinity for the capture components, to dissociate at least a portion of at least some of the plurality of molecules or particles from the first substrate, thereby forming a plurality of dissociated species, wherein at least some of the plurality of dissociated species comprise at least a portion of the enzymatic component;

detecting at least some of the plurality of dissociated species; and

determining a measure of the concentration of the analyte molecules or particles in the fluid sample based on the detection of the plurality of dissociated species.

52-77. -77. (canceled)

78. A method of detecting analyte molecules or particles in a fluid sample, comprising:

exposing a substrate comprising a plurality of capture components to a sample comprising a plurality of analyte molecules or particles, so that analyte molecules or particles associate with capture components to form a plurality of complexes, each complex being immobilized with respect to the substrate and comprising at least one capture component, at least one analyte molecule or particle, and at least one enzymatic component;

exposing the substrate to a dissociating agent to cause at least a portion of at least some of the plurality of complexes to dissociate from the substrate to form a plurality of dissociated species, which are not immobilized with respect to the substrate and wherein at least some of the dissociated species each comprise at least a portion of the enzymatic component; and

detecting a plurality of the dissociated species substantially simultaneously, wherein each of the detected dissociated species are spatially separated with respect to the other detected dissociated species during detection, such that detection is able to resolve individual dissociated species of the plurality of dissociated species.

79-87. -87. (canceled)