Exploring fluorophore microenvironments

• US 20060003320A1
• Filed: 07/01/2005
• Published: 01/05/2006
• Est. Priority Date: 07/02/2004
• Status: Active Grant

• Current Assignee: Blueshift Biotechnologies, Inc. (Danaher Corporation)
• Original Assignee: Blueshift Biotechnologies, Inc. (Danaher Corporation)
• Inventors: Miller, Steven C., Shumate, Christopher B., Comita, Paul B., Cromwell, Evan F.
• Granted Patent: US 7,141,378 B2
• Time in Patent Office: Days
• US Class Current: 435/5
• CPC Class Codes: B82Y 10/00 Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
• CPC Class Codes: B82Y 5/00 Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 2561/119 Fluorescence polarisation
• CPC Class Codes: C12Q 2563/107 fluorescence
• CPC Class Codes: G01N 2021/6419 Excitation at two or more wavelengths
• CPC Class Codes: G01N 2021/6421 Measuring at two or more wavelengths
• CPC Class Codes: G01N 2021/6432 Quenching
• CPC Class Codes: G01N 2021/6441 with two or more labels
• CPC Class Codes: G01N 2021/6478 Special lenses
• CPC Class Codes: G01N 2021/6484 Optical fibres
• CPC Class Codes: G01N 21/6408 with measurement of decay time, time resolved fluorescence
• 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 21/6445 Measuring fluorescence polarisation
• CPC Class Codes: G01N 2201/067 Electro-optic, magneto-optic, acousto-optic elements
• CPC Class Codes: G01N 2201/0697 Pulsed lasers
• CPC Class Codes: G01N 2201/0833 Fibre array at detector, resolving
• CPC Class Codes: G01N 33/582 with fluorescent label

Abstract

Methods, apparatus, and system, implementing and using techniques for detecting a presence of one or more target analytes in particular regions of interest of one or more samples. One or more samples including objects and one or more target analytes are provided. Some of the target analytes are labeled with a fluorophore and are bound to some of the objects in the samples. The samples are illuminated with fluorescence inducing light and fluorescent light is collected from one or more regions of the one or more samples. At least one anisotropy measurement of the samples is performed to identify regions of interest where one or more target analytes are bound to the objects. The collected fluorescent light from the regions of interest is analyzed to determine a presence of target analytes that are bound to the objects in the one or more samples.

Claims

1. A method for detecting a presence of one or more target analytes in particular regions of interest of one or more samples, the method comprising:

providing one or more samples including a plurality of objects and one or more target analytes, wherein at least some of the target analytes are labeled with a fluorophore and are bound to at least some of the objects in the one or more samples;

illuminating the one or more samples with fluorescence inducing light;

collecting fluorescent light from one or more regions of the one or more samples;

performing at least one anisotropy measurement of the one or more samples to identify one or more regions of interest where one or more target analytes are bound to the objects; and

analyzing the collected fluorescent light from the regions of interest to determine a presence of target analytes that are bound to the objects in the one or more samples.

2. The method of claim 1, wherein:

the regions of interest are identified as regions of the sample having a measured anisotropy value that exceeds a predetermined threshold value; and

collecting fluorescent light includes collecting fluorescent light only from confined detection regions within the identified regions of interest.

3. The method of claim 1, wherein:

the regions of interest are identified as regions of the sample having a measured anisotropy value that exceeds a predetermined threshold value; and

analyzing the fluorescent light includes only analyzing fluorescent light collected from the identified regions of interest.

4. The method of claim 1, wherein the objects are selected from the group consisting of:

spots, microbeads, cells, and microarrays

5. The method of claim 1, wherein at least some of the plurality of objects are optically encoded by one or more of:

fluorophores, quantum dots or other materials with a distinct response to excitation light.

6. The method of claim 1, wherein providing a sample includes:

providing a plurality of optically encoded objects, each optically encoded object having an affinity to an analyte and having an optical signature corresponding to the analyte;

contacting the objects with a sample containing one or more analytes having a first affinity moiety to at least one target analyte and a second affinity moiety to at least some of the optically encoded objects in the plurality of optically encoded objects, whereby the first affinity moiety of at least some analytes in the sample bind to the optically encoded objects; and

contacting the optically encoded objects and their bound analytes with a target sample containing one or more target analytes under conditions allowing the target analytes to bind to the second affinity moiety of the analytes in the sample.

7. The method of claim 1, wherein analyzing includes one or more of:

detecting a binding reaction occurring at one or more of the objects, classifying target analytes at one or more of the objects, and enumerating the one or more objects.

8. The method of claim 1, wherein the providing is performed under homogenous conditions that do not involve any wash steps.

9. The method of claim 6, wherein the second affinity moiety is selected from the group consisting of:

an antibody, an antigen, a receptor, a ligand, a nucleic acid, an enzyme, a substrate inhibitor, and an analogous moiety.

10. The method of claim 1, wherein the target analytes include one or more of:

an antibody, an antigen, a receptors, a ligand, a protein, a peptide, an enzyme, a nucleic acid, a drug, a hormone, a chemical, a pathogen, a toxin, a bacterium, or a virus.

11. The method of claim 1, wherein the collecting and analyzing steps are performed for up to about 20,000 objects per second.

12. The method of claim 5, wherein each optically encoded object is individually classifiable based on its emitted fluorescent light.

13. The method of claim 1, wherein the collecting step includes collecting one or more of:

fluorescence intensity values, fluorescence polarization values, fluorescence anisotropy values, rotational correlation times, and fluorescence lifetimes.

14. The method of claim 1, wherein the illuminating, collecting and analyzing steps are performed in multiple fluorescence wavelength regions.

15. The method of claim 1, wherein analyzing further comprises measuring changes with respect to time of the collected fluorescent light to provide kinetic information.

16. The method of claim 15, further including determining concentrations for the one or more target analytes based on measured changes in intensity values of the collected fluorescent light over time.

17. The method of claim 15, further including determining concentrations for the one or more target analytes based on measured changes in anisotropy values of the collected fluorescent light over time.

18. The method of claim 15, further including determining individual objects in the plurality of objects that contain bound target analytes based on measured changes in anisotropy values of the collected fluorescent light over time.

19. The method of claim 1, further comprising:

providing a plurality of objects, each object having a known anisotropy, whereby an internal anisotropy reference is formed; and

wherein performing at least one anisotropy measurement includes comparing the measured anisotropy to the anisotropy of the objects with known anisotropy in order to obtain an improved anisotropy measurement of the bound target analyte.