ULTRA-SENSITIVE DETECTION OF MOLECULES BY CAPTURE-AND-RELEASE USING REDUCING AGENTS FOLLOWED BY QUANTIFICATION

• US 20100075439A1
• 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: Walt, David R., Duffy, David C., Rissin, David M., Ferrell, Evan, Randall, Jeff
• Application Number:
  US12/236,488
• Publication Number:
  US 20100075439A1
• Time in Patent Office: Days
• US Class Current: 436/518
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms

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 and at least one analyte molecule or particle;

exposing the plurality of complexes to a reducing 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

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 at least some of the dissociated species.

2. The method of claim 1, wherein the reducing agent is beta-mercaptoethanol.

3. The method of claim 1, wherein the reducing agent is dithiothreitol.

4. The method of claim 1, wherein the reducing agent is tris(2-carboxyethyl) phosphine.

5. The method of claim 1, wherein the determining step comprises partitioning at least some of the dissociated species across a plurality of reaction vessels.

6. The method of claim 5, 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.

7. The method of claim 5, 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.

8. The method of claim 5, further comprising determining the number of the plurality of reaction vessels and/or fraction of the plurality of reaction vessels that contain or do not contain a dissociated species

9. The method of claim 8, wherein the number or fraction of the plurality of 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.

10. The method of claim 8, wherein the number or fraction of the plurality of reaction vessels that contain a dissociated species is directly proportional to the concentration of analyte molecules or particles in the sample.

11. The method of claim 8, wherein the number of the plurality of 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.

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

13. The method of claim 12, wherein the beads are magnetic.

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

15. The method of claim 5, wherein the plurality of reaction vessels is formed in the distal end of a fiber optic bundle.

16-39. -39. (canceled)

40. A system for detecting analyte molecules or particles in a fluid sample, comprising:

a first substrate comprising a plurality of capture components able to become specifically immobilized with respect to a plurality of analyte molecules or particles in the fluid sample, such that the analyte molecules or particles associate with capture components to form a plurality of complexes;

wherein at least a portion of at least some of the complexes is susceptible to being dissociated from the first substrate by exposure to a reducing agent, to form a plurality of dissociated species;

a second substrate configured to receive and contain dissociated species therein or thereon; and

a detector configured to detect dissociated species in or on the second substrate.

41-59. -59. (canceled)

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

capturing a plurality of analyte molecules or particles on a substrate;

causing at least a portion of at least some of the plurality of molecules or particles to dissociate from the substrate by exposing the plurality of molecules or particles to a reducing agent, thereby forming a plurality of dissociated species;

detecting at least a some of the dissociated species; and

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

61-68. -68. (canceled)

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

capturing a plurality of analyte molecules or particles on a first substrate by immobilizing the plurality of analyte molecules or particles on the first substrate;

exposing the first substrate to a reducing agent to cause a plurality of dissociated species to be released from the substrate;

detecting at least some of the plurality of dissociated species, wherein the number of dissociated species detected is no greater than the number of dissociated species released from the substrate in the exposing step and is also no greater than the number of analyte molecules or particles captured on the first substrate in the capturing step; and

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

70-76. -76. (canceled)

77. 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 disulfide linkage;

cleaving at least some of the disulfide linkages 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

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.

78-87. -87. (canceled)

88. 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 and at least one analyte molecule or particle;

exposing the plurality of complexes to a reducing 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

detecting at least some of the 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

89-97. -97. (canceled)