Methods and systems for extending dynamic range in assays for the detection of molecules or particles

• US 9,551,663 B2
• Filed: 02/15/2013
• Issued: 01/24/2017
• Est. Priority Date: 03/01/2010
• Status: Active Grant

• Current Assignee: Quanterix Corporation
• Original Assignee: Quanterix Corporation
• Inventors: Rissin, David M., Fournier, David, Duffy, David C.
• Primary Examiner(s): LAM, ANN Y
• Application Number:
  US13/768,843
• Publication Number:
  US 20130165342A1
• Time in Patent Office: 1,439 Days
• Field of Search: None
• US Class Current: 1/1
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates
• CPC Class Codes: G01N 33/50 Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing measuring or testing processes involving enzymes or microorganisms, compositions or test papers therefor; processes for forming such compositions, condition responsive control in microbiological or enzymological processes C12Q

Abstract

Described herein are systems and methods for extending the dynamic range of assay methods and systems used for determining the concentration of analyte molecules or particles in a fluid sample. In some embodiments, a method comprises spatially segregating a plurality of analyte molecules in a fluid sample into a plurality of locations. At least a portion of the locations may be addressed to determine the percentage of said locations containing at least one analyte molecule. Based at least in part on the percentage, a measure of the concentration of analyte molecules in the fluid sample may be determined using an analog, intensity-based detection/analysis method/system and/or a digital detection/analysis method/system. In some cases, the assay may comprise the use of a plurality of capture objects.

Claims

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

providing analyte molecules or particles immobilized with respect to a binding surface having affinity for at least one type of analyte molecule or particle, the binding surface forming or contained within one of a plurality of locations on a substrate;

addressing at least some of the plurality of locations and determining a measure indicative of the percentage of said locations containing at least one analyte molecule or particle; and

based upon the percentage, either determining a measure of the concentration of analyte molecules or particles in the fluid sample based at least in part on the number of locations containing at least one analyte molecule or particle or determining a measure of the concentration of analyte molecules or particles in the fluid sample based at least in part on a measured intensity of a signal that is indicative of the presence of a plurality of analyte molecules or particles.

2. The method of claim 1, wherein the analyte molecules or particles in a fluid sample comprise at least a first type of analyte molecule or particles and a second type of analyte molecules or particles.

3. The method of claim 2, comprising determining the percentage of said locations containing the first type of analyte molecules or particles and the percentage of said locations containing the second type of analyte molecules or particles;

based upon the percentage of said locations containing the first type of analyte molecules or particles, either 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 number of locations containing at least one first type of analyte molecule or particle or 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 a measured intensity of a signal that is indicative of the presence of a plurality of the first type of analyte molecules or particles; and

based upon the percentage of said locations containing the second type of analyte molecules or particles, either determining a measure of the concentration of the second type of analyte molecules or particles in the fluid sample based at least in part on the number of locations containing at least one first second of analyte molecule or particle or determining a measure of the concentration of the second type of analyte molecules or particles in the fluid sample based at least in part on a measured intensity of a signal that is indicative of the presence of a plurality of the second type of analyte molecules or particles.

4. The method of claim 1, wherein the binding surface comprises a plurality of capture objects.

5. The method of claim 4, wherein the plurality of capture objects comprise a plurality of beads.

6. The method of claim 1, further comprising at least one background signal determination.

7. The method of claim 1, wherein the measure of the concentration of analyte molecules in a fluid sample is based at least in part on comparison of a measured parameter to a calibration curve.

8. The method of claim 7, wherein the calibration curve is formed at least in part by determination of at least one calibration factor.

9. The method of claim 8, wherein the calibration factor is determined using a calibration sample wherein the percentage of locations containing at least one analyte molecule is between about 30% and about 50%.

10. The method of claim 1, wherein the measure of the concentration of analyte molecules in a fluid sample is based at least in part on a Poisson distribution adjustment.

11. The method of claim 1, wherein the percentage of said locations containing at least one analyte molecule or particle is determined using optical techniques.

12. The method of claim 11, wherein the optical techniques comprise the use of a CCD detector.

13. The method of claim 1, wherein the concentration of analyte molecules or particles in the fluid sample is less than about 50×

10<sup>−

15</sup> M.

14. The method of claim 1, wherein the analyte molecules or particles are proteins or nucleic acids.

15. The method of claim 1, wherein the analyte molecules or particles comprise an enzymatic component.

16. The method of claim 1, wherein the analyte molecules are exposed to at least one binding ligand under conditions such that substantially all of the analyte molecules associate with at least one binding ligand.

17. The method of claim 16, wherein the at least one binding ligand comprises an enzymatic component.

18. The method of claim 16, further comprising exposing the analyte molecules or particles to a precursor labeling agent.

19. The method of claim 18, wherein the precursor labeling agent is converted to a labeling agent upon exposure to the enzymatic component.

20. The method of claim 19, wherein the presence of an analyte molecule or particle at a location is determined by determining the presence of at least one precursor labeling agent.

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

providing a plurality of capture objects that each are associated with either at least one analyte molecule or particle or are free of any analyte molecules or particles;

individually addressing at least a portion of the capture objects and determining the percentage of said capture objects associated with at least one analyte molecule or particle; and

based upon the percentage, either determining a measure of the concentration of analyte molecules or particles in the fluid sample based at least in part on the number of locations containing a capture object associated with at least one analyte molecule or particle, or determining a measure of the concentration of analyte molecules or particles in the fluid sample based at least in part on a measured intensity level of a signal of that is indicative of the presence of a plurality of analyte molecules or particles.