METHODS RELATING TO IMPROVING ACCURACY OF CAPTURE OBJECT-BASED ASSAYS

• US 20180003703A1
• Filed: 01/13/2016
• Published: 01/04/2018
• Est. Priority Date: 01/13/2015
• Status: Abandoned Application

• Current Assignee: Quanterix Corporation
• Original Assignee: Quanterix Corporation
• Inventors: Duffy, David C., Rissin, David M., Fishburn, Matthew, Rivnak, Andrew, Patel, Purvish
• Application Number:
  US15/543,401
• Publication Number:
  US 20180003703A1
• Time in Patent Office: Days
• 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

Described herein are methods for improving the accuracy of capture object-based assays. In some embodiments, a measure of the number or a measure of the concentration of an analyte molecule or particle in a fluid sample is determined using the capture object-based assay. The subject matter of the present invention involves, in some cases, interrelated products, alternative solutions to a particular problem, and/or a plurality of different uses of one or more systems and/or articles.

Claims

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

exposing a plurality of capture objects to a solution containing or suspected of containing a first type of analyte molecules or particles, wherein the capture objects comprise a first type of capture object and one or more types of non-targeting capture objects,

wherein each of the first type of capture object includes a binding surface having specific binding affinity for the first type of analyte molecule or particle;

wherein each of the one or more types of non-targeting capture objects do not include any binding surfaces having specific binding affinity for any type of analyte molecules or particles contained in or suspected to be contained in the solution;

wherein the ratio of the number of first type of capture objects to the total number of capture objects is between 1;

1.2 and 1;

100; and

wherein at least some of the first type of capture objects associate with at least one analyte molecule or particle and at least some of the first type of capture objects do not associate with any analyte molecules or particles;

spatially separating at least a portion of the plurality of capture objects subjected to the exposing step into a plurality of separate locations;

addressing at least some of the plurality of locations and determining the number of locations containing a first type of capture object;

further determining the number of said locations containing a first type of capture object and a first type of analyte molecule or particle; and

determining a measure of the concentration of the first type of analyte molecules or particles in the fluid sample based at least in part on the ratio of the number of locations containing a first type of capture object and a first type of analyte molecule and particle, to the number of locations containing a first type of capture object.

12. The method of any preceding claim, wherein at least a portion of the capture objects subjected to the exposing step are spatially separating into a plurality of locations.

13. The method of any preceding claim, wherein the plurality of capture objects comprises a plurality of beads.

14. The method of any preceding claim, wherein the average diameter of the plurality of capture objects is between about 0.1 micrometer and about 100 micrometers.

15. The method of any preceding claim, wherein the average diameter of the plurality of capture objects is between about 1 micrometer and about 10 micrometers.

16. The method of any preceding claim, further comprising performing at least one wash step.

17. The method of any preceding claim, wherein the measure of the concentration of the at least one type of analyte molecule or particle, or the first type or analyte molecule or particle, and/or the second type of analyte molecule or particle is determined at least in part by comparison of a measured parameter to a calibration standard.

18. The method of any preceding claim, wherein the plurality of locations comprising a plurality of reaction vessels.

19. The method of any preceding claim, further comprising sealing the plurality of reaction vessels.

20. The method of any preceding claim, wherein the average volume of the plurality of reaction vessels is between about 10 attoliters and about 100 picoliters, or between about 1 femtoliter and about 100 femtoliters, or between about 1 femtoliter and about 1 picoliter, or between about 1 micrometer and about 10 micrometers.

21. The method of any preceding claim, wherein the plurality of locations is addressed using optical techniques.

22. The method of any preceding claim, wherein the at least one type of analyte molecule or particle, or the first type or analyte molecule or particle, or the second type of analyte molecule or particle are proteins or nucleic acids.

23. The method of any preceding claim, wherein the number of said locations containing the at least one type of analyte molecule or particle, or the first type or analyte molecule or particle, or the second type of analyte molecule or particle are determined using optical techniques.

24. The method of any preceding claim, wherein the ratio of the first type of capture object to the total number of capture objects is between 1:

2 and 1;

100, or between 1;

5 and 1;

100, or between 1;

5 and 1;

75, or between 1;

5 and 1;

50, or between 1;

5 and 1;

25, or between 1;

10 and 1;

100, or between 1;

10 and 1;

75, or between 1;

10 and 1;

50, or between 1;

20 and 1;

100, or between 1;

25 and 1;

100.

25. The method of any preceding claim, wherein the ratio of the second type of capture object to the total number of capture objects is between 1:

2 and 1;

100, or between 1;

5 and 1;

100, or between 1;

5 and 1;

75, or between 1;

5 and 1;

50, or between 1;

5 and 1;

25, or between 1;

10 and 1;

100, or between 1;

10 and 1;

75, or between 1;

10 and 1;

50, or between 1;

20 and 1;

100, or between 1;

25 and 1;

100.

26. The method of any preceding claim, wherein at least some of the first type of capture objects associate with at least one analyte molecule or particle and a statistically significant fraction of the first type of capture objects do not associate with any analyte molecules or particles.

27. The method of any preceding claim, wherein at least some of the second type of capture objects associate with at a second type of analyte molecule or particle and a statistically significant fraction of the second type of capture objects do not associate with any analyte molecules or particles.

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

exposing a plurality of capture objects to a solution containing or suspected of containing the first type of analyte molecules or particles, wherein the capture objects comprise a first type of capture object and one or more types of non-targeting capture objects,

wherein each of the first type of capture object includes a binding surface having specific binding affinity for the first type of analyte molecule or particle;

wherein each of the one or more types of non-targeting capture objects do not include any binding surfaces having specific binding affinity for the first type of analyte molecules or particles;

wherein the ratio of the first type of capture objects to the total number of capture objects is between 1;

1.2 and 1;

100; and

wherein at least some of the first type of capture objects associate with at least one analyte molecule or particle and at least some of the first type of capture objects do not associate with any analyte molecules or particles;

spatially separating at least a portion of the plurality of capture objects subjected to the exposing step into a plurality of separate locations;

addressing at least some of the plurality of locations and determining the number of locations containing a first type of capture object;

further determining the number of said locations containing a first type of capture object and a first type of analyte molecule or particle; and

determining a measure of the concentration of only the first type of analyte molecules or particles in the fluid sample based at least in part on the ratio of the number of locations containing a first type of capture object and a first type of analyte molecule and particle, to the number of locations containing a first type of capture object.

3. A method for determining a measure of the concentration of only a first type and a second type of analyte molecules or particles in a fluid sample, comprising:

exposing a plurality of capture objects to a solution containing or suspected of containing first types of analyte molecules or particles and a second type of analyte molecules or particles, wherein the capture objects comprise a first type of capture object, a second type of capture object, and one or more types of non-targeting capture objects,

wherein each of the first type of capture object includes a binding surface having affinity for the first type of analyte molecule or particle;

wherein each of the second type of capture object includes a binding surface having affinity for the second type of analyte molecule or particle; and

wherein each of the one or more types of non-targeting capture objects do not include any binding surfaces having affinity for the first type of analyte molecules or particles or the second type of analyte molecules or particles;

wherein the ratio of the first type of capture objects to the total number of capture objects and the ratio of the second type of capture objects to the total number of capture objects are the same or different and are between 1;

1.2 and 1;

100;

wherein at least some of the first type of capture objects associate with at least one analyte molecule or particle and at least some of the first type of capture objects do not associate with any analyte molecule or particle; and

wherein at least some of the second type of capture objects associate with at least some of the second type of analyte molecule or particle at least some of the second type of capture objects do not associate with any analyte molecule or particle;

spatially separating at least a portion of the capture objects subjected to the exposing steps into a plurality of separate locations;

addressing at least some of the plurality of locations and determining the number of locations containing a first type capture object or a second type of capture object;

further determining the number of said locations containing a first type of analyte molecule or particle or a second type of analyte molecule or particle; and

determining a measure of the concentration of only the first type of analyte molecules or particles and the second type of analyte molecules or particles in the fluid sample based at least in part on the ratio of the number of locations containing a first type of capture object and a first type of analyte molecule and particle, to the number of locations containing a first type of capture object, or based at least in part on the ratio of the number of locations containing a second type of capture object and a second type of analyte molecule and particle, to the number of locations containing a second type of capture object, respectively.

4. A method for binding analyte molecules or particles in a fluid sample to capture objects and spatially separating the capture objects, comprising:

exposing a plurality of capture objects to a solution comprising or derived from the fluid sample, wherein the capture objects comprise at least one type of targeting capture objects and at least one type of non-targeting capture objects,

wherein each of the at least one type of targeting capture objects includes a binding surface having specific binding affinity for at least one type of target analyte molecule or particle contained in or suspected to be contained in the solution,

wherein each of the one or more types of non-targeting capture objects do not include any binding surfaces having specific binding affinity for any of the at least one type of target analyte molecule or particle contained in or suspected to be contained in the solution,

wherein the ratio of the number of targeting capture objects to the total number of targeting and non-targeting capture objects is between 1;

1.2 and 1;

100;

spatially separating at least a portion of the plurality of capture objects subjected to the exposing step.

5. The method of claim 4, further comprising:

addressing at least some of the spatially separated capture objects and determining the number of the at least one type of analyte molecules associated with a capture objects.

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

exposing a plurality of capture objects to a solution containing or suspected of containing a first type of analyte molecules or particles, wherein the capture objects comprise a first type of capture object and a second type of capture object;

exposing the plurality of capture objects to a second type of analyte molecules or particles,

wherein;

each of the first type of capture object includes a binding surface having specific binding affinity for the first type of analyte molecule or particle;

each of the second type of capture objects do not include any binding surfaces having specific binding affinity for the first type of analyte molecules or particles contained in or suspected to be contained in the solution and include at least one binding surface having some affinity for the second type of analyte molecule or particle;

at least some of the first type of capture objects associate with at least one analyte molecule or particle and at least some of the first type of capture objects do not associate with any analyte molecules or particles,

a statistically significant fraction of the second type of capture objects associate with either zero or one of the second type of analyte molecules or particles, and

the ratio of the number of first type of capture objects to the total number of capture objects is between 1;

1.2 and 1;

100;

spatially separating at least a portion of the plurality of capture objects subjected to the exposing step into a plurality of separate locations;

addressing at least some of the plurality of locations and determining the number of locations containing a first type of capture object;

further determining the number of the locations determined to contain a first type of capture object that also contain a first type of analyte molecule or particle;

addressing at least some of the plurality of locations and determining which locations contain a second type of capture object and a binding ligand;

further determining the average intensity of said locations containing a second type of capture object and a second type of analyte molecule or particle; and

determining a measure of the concentration of the first type of analyte molecules or particles in the fluid sample based at least in part on the average intensity of said locations containing a second type of capture object and a second type of analyte molecule or particle.

7. The method of claim 6, wherein the second type of capture objects include at least one binding surface having specific affinity for the second type of analyte molecule.

8. The method of claim 6 or 7, wherein the second type of analyte molecule is a binding ligand used in the detection of the first type of analyte molecule.

9. The method of claim 8, wherein the binding ligand may be detected directly or indirectly.

10. The method of claim 6 or 7, wherein the second type of analyte molecule is different than the first type of analyte molecule and is added to the fluid sample in a known concentration.

11. The method of claim 10, wherein the second type of analyte molecule is detected indirectly.