Single molecule detection by in situ hybridization

• US 5,866,331 A
• Filed: 10/20/1995
• Issued: 02/02/1999
• Est. Priority Date: 10/20/1995
• Status: Expired due to Fees

• Current Assignee: University Of Massachusetts
• Original Assignee: University Of Massachusetts
• Inventors: Femino, Andrea M., Singer, Robert H.
• Primary Examiner(s): Chambers, Jasemine C.
• Assistant Examiner(s): PRIEBE, SCOTT DAVID
• Application Number:
  US08/546,072
• Time in Patent Office: 1,201 Days
• Field of Search: 435/6, 359/396, 422/82.08, 250/459.1
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 1/6841 In situ hybridisation

Abstract

Disclosed are methods for accurately determining the total emission intensity of a single fluorochrome, under imaging conditions, using a digital imaging fluorescence microscopy system. Also disclosed are methods for detecting and localizing probe-target molecule binding. The detection method has sufficient resolution and sensitivity to locate and detect a single target-bound probe.

Claims

1. A method for digital imaging fluorescence microscopy detection of an individual nucleic acid probe bound to a nucleic acid target molecule in a sample, said method comprising the steps of:

(a) obtaining a fluorochrome-labeled nucleic acid probe wherein the number of fluorochromes per probe is predetermined;

(b) contacting said labeled probe with a nucleic acid target molecule under conditions allowing said labeled probe to bind to said target molecule;

(c) removing unbound labeled probes from labeled probes bound to target molecules;

(d) detecting, by digital imaging fluorescence microscopy, said labeled probe bound to said target molecule, wherein said digital imaging fluorescence microscopy includes digitally recording a series of optical sections;

(e) determining the total fluorescence intensity per fluorochrome under imaging conditions;

(f) determining the total fluorescence intensity per probe from said total fluorescence intensity per fluorochrome;

(g) normalizing said total fluorescence intensity per fluorochrome under imaging conditions to a value for a single conjugated fluorochrome whose image is acquired through a series of optical sections and restored, thereby producing a normalized total fluorescence intensity;

(h) producing a prepared image from said series of optical sections by subjecting said series of optical sections, sequentially, to dark current subtraction, background subtraction, and normalization to the first optical section;

(i) producing a restored image;

(j) identifying discrete objects in said restored image, said objects corresponding to target molecules;

(k) comparing said normalized total fluorescence intensity to values of objects in said restored image;

(l) determining the presence of one or more probes in one of said objects, thereby detecting an individual nucleic acid probe bound to a nucleic acid target molecule in a sample.

2. The method of claim 1, wherein said restored image is produced by subjecting a prepared image to exhaustive photon reassignment.

3. The method of claim 2, wherein a threshold is applied to pixels in said restored image by preparing a restored image of a negative control cell subjected to a mock in situ hybridization protocol wherein no probe is present, and selecting a total fluorescence intensity threshold value based on one or more measurements relating to said negative control cell.

4. The method of claim 1, wherein said probe is an oligonucleotide linked to a fluorochrome label, said target molecule is a nucleic acid, and said binding is in situ nucleic acid hybridization.

5. The method of claim 4, wherein the length of said oligonucleotide is from 20 to 200 nucleotides.

6. The method of claim 5, wherein the length of said oligonucleotide is from 40 to 100 nucleotides.

7. The method of claim 4, wherein said fluorochrome label is covalently attached to a functional group on a modified base incorporated into said oligonucleotide.

8. The method of claim 7, wherein said functional group is a primary amino group.

9. The method of claim 7, wherein said functional group is at the end of a spacer arm.

10. The method of claim 4, wherein said oligonucleotide comprises a multiplicity of modified bases with attached fluorochromes.

11. The method of claim 10, wherein said modified bases are incorporated at intervals of seven to thirteen base positions in the nucleotide sequence of said oligonucleotide.

12. The method of claim 1, wherein the fluorochrome is selected from the group consisting of CY3 and fluorescein.

13. The method of claim 4, wherein said nucleic acid is a DNA molecule.

14. The method of claim 4, wherein said nucleic acid is an RNA molecule.

15. The method of claim 1, wherein said total fluorescence intensity per fluorochrome under imaging conditions is determined by a method comprising the steps of:

(a) providing a microscope slide and coverslip;

(b) providing on the surface of said microscope slide a first fluorescence point source;

(c) providing on the surface of said coverslip a second fluorescence point source;

(d) preparing a standard solution containing a known concentration of fluorochrome-labeled probes;

(e) placing a suitable volume of said standard solution between and in contact with said microscope slide and said coverslip, said first fluorescence point source and said second fluorescence point source being within the field of view of said digital imaging microscopy system;

(f) determining a distance between said first and second fluorescence point sources, thereby obtaining a z axis distance between said microscope slide and said coverslip;

(g) determining an imaged volume by determining the product of an x axis distance, a y axis distance, and said z axis distance;

(h) determining the total amount of probe fluorescence from the imaged volume;

(i) calculating the total number of probes in the imaged volume using (1) said known concentration of probes in said standard solution, and (2) said imaged volume; and

(j) dividing the total amount of probe fluorescence from said imaged volume by the number of fluorochromes in the imaged volume to determine the total fluorescence intensity of a single fluorochrome under imaging conditions.

16. The method of claim 3, wherein said threshold is determined and applied to a sample by:

(a) preparing a restored image of a negative control cell subjected to a mock in situ hybridization protocol wherein no probe is present;

(b) obtaining a frequency distribution of light in said negative control cell and calculating the mean and standard deviation of said frequency distribution;

(c) selecting a total fluorescence intensity threshold value based on said mean and standard deviation;

(d) excluding all optical data other than that originating from within the sample, thereby producing a masked image; and

(e) setting to a value of zero all pixels whose total fluorescence intensity value is below said total fluorescence intensity threshold value in said masked image.

17. The method of claim 2, wherein said nucleic acid is a viral nucleic acid, and said method is used to diagnose a viral infection.

18. The method of claim 17, wherein said viral infection is HIV infection.

19. The method of claim 4, wherein said nucleic acid is a chromosome, and said method is used to diagnose a genetic defect.

20. The method of claim 19, wherein said genetic defect is a trinucleotide repeat expansion.

21. The method of claim 1, wherein the presence of one or more probes in an object is determined based on the total fluorescence intensity of said object and the total fluorescence intensity per probe.

22. A method for determining the total fluorescence intensity of a single fluorochrome in a digital imaging microscopy system, under imaging conditions, said method comprising the steps of:

(a) providing a microscope slide and coverslip;

(b) providing on the surface of said microscope slide a first fluorescence point source;

(c) providing on the surface of said coverslip a second fluorescence point source;

(d) preparing a standard solution containing a known concentration of fluorochrome-labeled probes;

(e) placing a suitable volume of said standard solution between and in contact with said microscope slide and said coverslip, said first fluorescence point source and said second fluorescence point source being within the field of view of said digital imaging microscopy system;

(f) determining a distance between said first and second fluorescence point sources, thereby obtaining a z axis distance between said microscope slide and said coverslip;

(g) determining an imaged volume by determining the product of an x axis distance, a y axis distance, and said z axis distance;

(h) determining the total amount of probe fluorescence from the imaged volume;

(i) calculating the total number of probes in the imaged volume using (1) said known concentration of probes in said standard solution, and (2) said imaged volume; and

(j) dividing the total amount of probe fluorescence from said imaged volume by the number of fluorochromes in the imaged volume to determine the total fluorescence intensity of a single fluorochrome under imaging conditions.

23. The method of claim 22, wherein said first fluorescence point source and said second fluorescence point source are beads bearing a fluorochrome label.

24. The method of claim 23, wherein said beads have a diameter between 50 and 800 nanometers.

25. The method of claim 23, wherein said beads have a diameter between 100 and 400 nanometers.

26. The method of claim 23, wherein said beads have a diameter of approximately 200 nanometers.

27. A kit for use in determining the total fluorescence intensity of a single fluorochrome in a digital imaging microscopy system under imaging conditions, said kit comprising:

(a) a spotted microscope slide comprising fluorescent material on at least one surface, said material being deposited on said surface as a discrete slide spot, thereby forming a spotted microscope slide surface, said slide spot having a diameter and a thickness between 1 and 400 nanometers; and

(b) a spotted coverslip comprising fluorescent material on at least one surface, said material being deposited on said surface as a discrete coverslip spot, thereby forming a spotted coverslip surface, said coverslip spot having a diameter and a thickness between 1 and 400 nanometers;

wherein said spotted microscope slide and said spotted coverslip can be used in combination, with said spotted microscope slide surface and said spotted coverslip surface opposing each other, so that said microscope slide spot and said coverslip spot are simultaneously visible within the field of view of a microscope.