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

• US 9,846,155 B2
• Filed: 08/17/2015
• Issued: 12/19/2017
• 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:
  US14/827,815
• Publication Number:
  US 20150355182A1
• Time in Patent Office: 855 Days
• Field of Search: None
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates
• CPC Class Codes: G01N 2201/062 LED's
• CPC Class Codes: G01N 2333/924 acting on glycosyl compounds (3.2)
• CPC Class Codes: G01N 33/54313 the carrier being characterised by its particulate form
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing
• CPC Class Codes: G01N 33/573 for enzymes or isoenzymes

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 a plurality of a first type 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;

providing a plurality of a second type of capture objects that are free of any analyte molecules or particles, wherein the second type of capture objects are distinguishable from the first type of capture objects;

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

addressing at least a portion of the second type of capture objects and determining at least one signal; 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 percentage or particle or determining a measure of the concentration of analyte molecules or particles in the fluid sample based at least in part on the at least one signal and 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 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.

3. The method of claim 2, wherein the calibration curve is formed at least in part by determination at least one calibration factor.

4. 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.

5. The method of claim 1, wherein the percentage of said first type of capture objects associated with at least one analyte molecule or particle is determined using optical techniques.

6. The method of claim 1, wherein the plurality of the first type of capture objects and the second type of capture objects are spatially separating into a plurality of locations prior to the addressing steps, and wherein the plurality of locations comprises a plurality of reaction vessels.

7. The method of claim 6, wherein the plurality of reaction vessels is formed on the end of a fiber optic bundle.

8. The method of claim 6, further comprising sealing the plurality of reaction vessels.

9. The method of claim 6, wherein the average volume of the plurality of reaction vessels is between about 1 femtoliter and about 1 picoliter.

10. 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.

11. The method of claim 1, wherein the percentage of locations addressed in the addressing step is at least about 5% of the total number of locations.

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

13. The method of claim 1, further comprising performing at least one wash step.

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

15. 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.

16. The method of claim 15, wherein the at least one binding ligand comprises an enzymatic component.

17. The method of claim 15, further comprising exposing the analyte molecules or particles to a precursor labeling agent.

18. The method of claim 17, wherein the precursor labeling agent is converted to a labeling agent upon exposure to the enzymatic component.

19. The method of claim 18, wherein the presence of an analyte molecule or particle is determined by determining the presence of at least one precursor labeling agent.