Fluorescence polarization assay system and method

• US 6,455,861 B1
• Filed: 09/14/1999
• Issued: 09/24/2002
• Est. Priority Date: 11/24/1998
• Status: Expired due to Term

• Current Assignee: Cambridge Research & Instrumentation Incorporated (Revvity, Inc.)
• Original Assignee: Cambridge Research & Instrumentation Incorporated (Revvity, Inc.)
• Inventors: Hoyt, Clifford C.
• Primary Examiner(s): Epps, Georgia
• Assistant Examiner(s): HANIG, RICHARD E
• Application Number:
  US09/395,661
• Publication Number:
  US 20020070349A1
• Time in Patent Office: 1,106 Days
• Field of Search: 250/458.1, 250/459.1, 250/461.1, 250/462.2, 250/252.1 R, 356/318, 356/417, 356/317
• US Class Current: 250/458.1
• CPC Class Codes: G01N 21/6445 Measuring fluorescence polarisation

Abstract

An instrument is disclosed for fluorescence assays which is capable of reading many independent samples at the same time. This instrument provides enhanced throughput relative to single-sample instruments, and is well-suited to use in general fluorescence, time-resolved fluorescence, multi-band fluorescence, fluorescence resonance energy transfer (FRET), and fluorescence polarization. This invention is beneficial in applications such as high-throughput drug screening, and automated clinical testing. Also disclosed are means and methods for a fluorescence polarization measurement which is highly sensitive, inherently self-calibrated, and unaffected by lamp flicker or photobleaching. This fluorescence polarization invention can be practiced on a variety of fluorescence instruments, including prior-art equipment such as microscopes and multi-well plate readers.

Claims

1. A fluorescence measurement instrument comprising

a plurality of sample regions for receiving samples;

excitation means that produce a first beam;

a diffractive optical beamsplitter element that splits the first beam into plural secondary beams, said plural secondary beams simultaneously exciting the plurality of sample regions to effect fluorescence of samples therein; and

detection means for detecting the fluorescence from the plurality of sample regions.

2. The fluorescence measurement instrument of claim 1, wherein the detection means comprise a detector with plural independent pixel regions for receiving the plural secondary beams.

3. The fluorescence measurement instrument of claim 1, wherein the plurality of sample regions is a multiwell plate having a plurality of wells having well walls separated by inter-sample regions, and

wherein the plural secondary beams provide substantially no illumination of the well walls or the inter-sample regions.

4. The fluorescence measurement instrument of claim 1 wherein the excitation means comprise a laser source.

5. A fluorescence measurement instrument comprising

excitation means for providing light;

a sample region;

detection means comprising an objective for gathering fluorescence emitted by said sample region and a photodetector for measuring the intensity of the fluorescence gathered by the objective; and

a mirror located between the sample region and the objective for directing light from the excitation means to the sample region, the mirror being small relative to the objective such that a substantial portion of the fluorescence emitted by the sample region towards the objective reaches the objective without impinging on the mirror.

6. The fluorescence measurement instrument of claim 5 wherein the excitation means comprise a laser source.

7. The fluorescence measurement instrument of claim 5, wherein the light of the excitation means is reflected by the mirror substantially at right angles onto the sample, and the mirror is located in a path of emission light from the sample to the objective.

8. The fluorescent measurement instrument of claim 5, wherein said mirror reflects substantially all of the light incident thereon.

9. A fluorescence polarization measurement instrument comprising

at least one sample region for receiving a sample;

excitation means for producing light that is substantially linearly polarized along a first axis of polarization at the sample region;

detection means that comprise an objective, a photodetector, and a polarization beam separator;

wherein the photodetector provides a plurality of spatially distinct pixel regions;

the objective directs a beam of fluorescent light from the sample toward the polarization beam separator;

the polarization beam separator divides the beam of fluorescent light into two linearly polarized secondary beams, one with polarization axis oriented substantially parallel to the first axis of polarization and the other with polarization axis oriented substantially perpendicular to the first axis of polarization; and

the secondary beams of fluorescent light are directed onto the spatially distinct pixel regions of the photodetector by the polarization beam separator.

10. The fluorescence polarization measurement instrument of claim 9, wherein the polarization beam separator is a planar element of doubly refractive material.

11. The fluorescence polarization measurement instrument of claim 10, wherein the polarization beam separator is made of calcite.

12. The fluorescence polarization measurement instrument of claim 10, wherein the polarization beam separator further comprises a second birefringent element that equalizes the optical path length between the two linearly polarized secondary beams.

13. A fluorescence polarization measurement instrument comprising:

at least one sample region for receiving a sample;

excitation means for producing light that is directed at the sample region to effect fluorescent emission of the sample and that is substantially linearly polarized along a first axis of polarization at the sample region;

detection means that comprise an objective, a plurality of independent detector regions, and a polarization beam separator;

wherein the plurality of independent detector regions comprises one of a unitary detector with multiple pixel regions and multiple detectors;

the objective collects the fluorescent emission from the sample region and directs the fluorescent emission in a beam toward the polarization beam separator;

the polarization beam separator divides the beam of fluorescent emission into two linearly polarized secondary beams, one with polarization axis oriented substantially parallel to the first axis of polarization and the other with polarization axis oriented substantially perpendicular to the first axis of polarization;

the linearly polarized secondary beams are directed by the polarization beam separator to separate detector regions; and

said excitation means further provide switching means for changing the state of polarization of the excitation light at the sample region during a single fluorescence polarization measurement from a first orientation parallel to the first axis of polarization to a second orientation parallel to a second axis of polarization which is substantially perpendicular to the first axis of polarization.

14. The fluorescence polarization measurement instrument of claim 13 wherein the switching means are automated and do not require input to effect the changing of the state of polarization of the excitation light from the first orientation to the second orientation.

15. The fluorescence polarization measurement instrument of claim 14, wherein the switching means comprise a liquid crystal cell and associated drive circuitry.

16. The fluorescence polarization measurement instrument of claim 14, wherein the plural independent detector regions comprise a plurality of pixel regions on a unitary detector and the polarization beam separator comprises a planar element of doubly refractive material.

17. The fluorescence polarization measurement instrument of claim 15, wherein the plural independent detector regions comprise a plurality of pixel regions on a unitary detector and the polarization beam separator comprises a planar element of doubly refractive material.

18. The fluorescence polarization measurement instrument of claim 13, further comprising:

calculation means wherein the fluorescence polarization is calculated from four readings comprising an intensity of emission light of a first orientation generated from excitation light of a first orientation, an intensity of emission light of a second orientation generated from excitation light of a first orientation, an intensity of emission light of a first orientation generated from excitation light of a second orientation, an intensity of emission light of a second orientation generated from excitation light of a second orientation.

19. The fluorescence polarization measurement instrument of claim 14 which measures a plurality of sample regions simultaneously.

20. The fluorescence polarization measurement instrument of claim 19 where the plurality of sample regions comprise one of a linear array of points and a two-dimensional array of points.

21. The fluorescence polarization measurement instrument of claim 18 which measures a plurality of sample regions simultaneously.

22. The fluorescence polarization measurement instrument of claim 21, wherein the switching means comprise a liquid crystal cell and associated drive circuitry, and

the plurality of independent detector regions comprise a plurality of pixel regions on a unitary detector and the polarization beam separator comprises a planar element of doubly refractive material.

23. The fluorescence polarization measurement instrument of claim 13, further comprising:

a means for monitoring the light substantially linearly polarized along a first axis of polarization which is produced by the excitation means, wherein said monitoring means provides feedback to adjust a polarization of the light produced by the excitation means.

24. The fluorescence polarization measurement instrument of claim 23, wherein the means for monitoring comprises:

a reflecting means for reflecting the light substantially linearly polarized along a first axis of polarization which is produced by the excitation means;

a polarization filtering means for receiving reflected light from the reflecting means, for only transmitting a component of the reflected light that is substantially linearly polarized along an axis of polarization to be monitored, and for not transmitting any other components; and

a detector for receiving the transmitted component from the polarization filtering means and for detecting an intensity of said transmitted component.

25. The fluorescence polarization measurement instrument of claim 18, wherein the calculation means calculates the fluorescence polarization by the equation:

$1000*\frac{A-B+D-C}{A+B+D+C}$

where A is the intensity of emission light of a first orientation generated from excitation light of a first orientation;

B is the intensity of emission light of a second orientation generated from excitation light of a first orientation;

C is the intensity of emission light of a first orientation generated from excitation light of a second orientation; and

D is the intensity of emission light of a second orientation generated from excitation light of a second orientation.

26. The fluorescence polarization measurement instrument of claim 18, wherein the calculation means calculates the fluorescence polarization by the equation:

$1000*\frac{A-B+\mathrm{\gamma <br><br>}<br><br>\left(D-C\right)}{A+B+\mathrm{\gamma <br><br>}<br><br>\left(D+C\right)}$$\mathrm{where}<br><br>\text{\hspace{1em}<br><br>}<br><br>\mathrm{\gamma <br><br>}={\left[\frac{A*B}{C*D}\right]}^{\frac{1}{2}}$

and where A is the intensity of emission light of a first orientation generated from excitation light of a first orientation;

B is the intensity of emission light of a second orientation generated from excitation light of a first orientation;

C is the intensity of emission light of a first orientation generated from excitation light of a second orientation; and

D is the intensity of emission light of a second orientation generated from excitation light of a second orientation.

27. A fluorescence polarization measurement instrument comprising

at least one sample region for receiving a sample;

excitation means for providing plural beams of excitation light that are directed at the at least one sample region to effect fluorescent emission and that are substantially linearly polarized along a first axis of polarization at the at least one sample region;

detection means that comprise an objective, plural independent detector regions, and a polarization beam separator;

wherein a principal ray of each of the plural beams of excitation light is substantially parallel to an optical axis of the objective.

28. The fluorescence polarization measurement instrument of claim 27, wherein the objective is telecentric at the at least one sample region.

29. A method of measuring fluorescence polarization of a sample, comprising

illuminating the sample to effect fluorescence emission with a beam of excitation light that is linearly polarized along a first axis;

measuring the intensities of a first component of the fluorescence emission that is polarized along the first axis and a second component of the fluorescence emission that is polarized orthogonal to the first axis while the sample is illuminated with the beam of excitation light that is linearly polarized along the first axis;

switching the state of polarization of the beam of excitation light to a polarization state wherein said beam is linearly polarized along a second axis substantially orthogonal to the first axis;

measuring the intensities of a third component of fluorescence emission that is polarized along the first axis and a fourth component that is polarized orthogonal to the first axis while the sample is illuminated with the beam that is linearly polarized along the second axis; and

calculating the fluorescence polarization of the sample based on the measurements of the intensities of the first, second, third and fourth components.

30. The method of measuring fluorescence polarization of claim 29, wherein the measurements of the intensities of the orthogonal components of fluorescence emission are made simultaneously.

31. The method of measuring fluorescence polarization of claim 29, wherein the fluorescence polarization is calculated using a self-calibrating algorithm that compensates for at least one of variations in intensity in the first beam, differing responsivity between measurements of the two orthogonal components of fluorescence emission, and photobleaching of the sample.

32. The method of measuring fluorescence polarization of claim 29, wherein the fluorescence polarization is calculated by the equation:

$1000*\frac{A-B+D-C}{A+B+D+C}$

where A is the intensity of the first component;

B is the intensity of the second component;

C is the intensity of the third component; and

D is the intensity of the fourth component.

33. The method of measuring fluorescence polarization of claim 29, wherein the fluorescence polarization is calculated by the equation:

$1000*\frac{A-B+\mathrm{\gamma <br><br>}<br><br>\left(D-C\right)}{A+B+\mathrm{\gamma <br><br>}<br><br>\left(D+C\right)}$$\mathrm{where}<br><br>\text{\hspace{1em}<br><br>}<br><br>\mathrm{\gamma <br><br>}={\left[\frac{A*B}{C*D}\right]}^{\frac{1}{2}}$

and where A is the intensity of the first component;

B is the intensity of the second component;

C is the intensity of the third component; and

D is the intensity of the fourth component.

34. A method of measuring fluorescence of a sample, comprising:

providing an excitation beam of light;

positioning a mirror between the sample and an objective which collects the fluorescence emission from the sample;

reflecting the excitation beam of light from the mirror onto the sample to effect fluorescence emission, the mirror being small in size relative to the objective such that a substantial portion of the fluorescence emitted by the sample reaches the objective without impinging on the mirror; and

directing the fluorescence emission collected by the objective to a detection means for measurement.

35. The method of measuring fluorescence of claim 34, further comprising the step of:

selecting the size of the mirror such that the mirror does not completely block the fluorescence emission from collection by the objective.

36. The method of measuring fluorescence of claim 34, further including the steps of polarizing the excitation beam of light along a first linear polarization axis, analyzing the state of polarization of the fluorescence emission and determining the degree of fluorescence polarization of the sample.

37. The method of measuring fluorescence of claim 34, wherein all optical filters through which emission light travels in passing from sample to detection means are oriented substantially normal to an optical axis.

38. The method of claim 37, further including the steps of analyzing the state of polarization of the fluorescence emission and determining the degree of fluorescence polarization of the sample.

39. The method of claim 38, wherein the sample exhibits a maximum emission wavelength that is less than 20 nm from the maximum excitation wavelength.

40. The method of claim 38, where the sample comprises a Bodipy probe.

41. The method of claim 38 where the sample comprises an Alexa probe.

42. The method of claim 38, further including the steps of:

separating the emission light into a first component which is polarized along a first polarization axis and a second component which is polarized along a second polarization axis orthogonal to the first linear polarization axis; and

measuring both components simultaneously.

43. The method of claim 42, further including the steps of:

rotating the plane of polarization of the excitation beam from the first polarization axis to a second polarization axis substantially perpendicular to the first axis;

separating the emission light into a third component which is polarized along the first polarization axis and a fourth component which is polarized along the second polarization axis; and

measuring both components simultaneously while the excitation beam is polarized along said second axis.

44. The method of claim 42 further including the step of calculating the fluorescence polarization from the measurements of the two polarized components of the emission light.

45. The method of claim 43 further including the step of calculating the fluorescence polarization from the four measurements comprising the intensity of the two polarized components of the emission light when said excitation beam is polarized along said first polarization axis, and when said excitation beam is polarized along said second polarization axis.

46. The method of claim 45 where the fluorescence polarization is calculated using an algorithm that compensates for one of variations in intensity in the first beam, differing responsivity between measurements of the two components of emission light, and photobleaching of the sample.

47. The method of claim 45 wherein the sample exhibits a separation of 20 nm or less between the wavelength of peak absorption and the wavelength of peak emission.

48. The method of claim 47 where the sample comprises a Bodipy probe.

49. The method of claim 47 where the sample comprises an Alexa probe.

50. The method of measuring fluorescence claim 34, wherein the light of the excitation means is reflected by the mirror substantially at right angles onto the sample, and the mirror is located substantially in a path of emission light from the sample to the objective.

51. The method of claim 45, wherein the step of calculating the fluorescence polarization uses the equation:

$1000*\frac{A-B+D-C}{A+B+D+C}$

where A is an intensity of the first component;

B is an intensity of the second component;

C is the intensity of the third component; and

D is the intensity of the fourth component.

52. The method of claim 45, wherein the step of calculating the fluorescence polarization uses the equation:

$1000*\frac{A-B+\mathrm{\gamma <br><br>}<br><br>\left(D-C\right)}{A+B+\mathrm{\gamma <br><br>}<br><br>\left(D+C\right)}$$\mathrm{where}<br><br>\text{\hspace{1em}<br><br>}<br><br>\mathrm{\gamma <br><br>}={\left[\frac{A*B}{C*D}\right]}^{\frac{1}{2}}$

and where A is the intensity of the first component;

B is the intensity of the second component;

C is the intensity of the third component; and

D is the intensity of the fourth component.

53. The method of measuring fluorescence of claim 34, further comprising the step of:

selecting the size of the mirror such that the mirror does not substantially block the fluorescence emission from collection by the objective.

54. A method of determining the integrity of a sample for fluorescence measurement, comprising

providing a sample;

providing a beam of excitation light that is directed toward the sample;

collecting emission light from the sample with an objective; and

recording an image of said sample on a detector, said image being recorded with multiple independent pixel regions arranged in a two-dimensional array;

wherein the size of the pixel regions is chosen so the recorded image is comprised of enough pixel regions to produce a spatial distribution of intensity readings;

recording a spatial distribution of detector intensity readings for pixel regions within the recorded image; and

determining a measurement integrity of the sample based on a shape and uniformity of the spatial distribution of detector intensity readings, where an abnormal distribution indicates that the sample is suspect.

55. The method of claim 54 further including the steps of polarizing the excitation light along a first linear polarization axis, analyzing the state of polarization of the emission light and determining the degree of fluorescence polarization.

56. A method for taking a fluorescence polarization measurement comprising:

exciting a sample with excitation light of a first polarization;

separating resulting emission light from the sample into first and second orthogonally polarized components;

detecting intensities of the first and second components;

exciting the sample with excitation light of a second polarization orthogonal to said first polarization;

separating resulting emission light from the sample into third and fourth orthogonally polarized components wherein said third component has the same polarization as one of said first and second components and said fourth component has the same polarization as the other of said first and second components;

detecting intensities of the third and fourth components; and

calculating the fluorescence polarization using a self-calibrating equation that compensates for at least one of variations in intensity of the excitation light of the first polarization, differing responsivity between measurements of the two orthogonal components of fluorescence emission, and photobleaching of the sample.

57. The method of claim 56, wherein the step of calculating the fluorescence polarization uses the self-calibrating equation:

$1000*\frac{A-B+D-C}{A+B+D+C}$

where A is an intensity of the first component;

B is an intensity of the second component;

C is the intensity of the third component; and

D is the intensity of the fourth component.

58. The method of claim 56, wherein the step of calculating the fluorescence polarization uses the self-calibrating equation:

$1000*\frac{A-B+\mathrm{\gamma <br><br>}<br><br>\text{\hspace{1em}<br><br>}<br><br>\left(D-C\right)}{A+B+\mathrm{\gamma <br><br>}<br><br>\text{\hspace{1em}<br><br>}<br><br>\left(D+C\right)}$$\mathrm{where}<br><br>\text{\hspace{1em}<br><br>}<br><br>\mathrm{\gamma <br><br>}={\left[\frac{A*B}{C*D}\right]}^{\frac{1}{2}}$

and where A is the intensity of the first component;

B is the intensity of the second component;

C is the intensity of the third component; and

D is the intensity of the fourth component.

59. The method of claim 56, wherein said step of detecting the intensity of said first and second components comprises simultaneously detecting the intensity of said first and second components and wherein the step or detecting the intensity of said third and fourth components comprises simultaneously measuring the intensity of said third and fourth components.

60. A method of determining the integrity of a sample for fluorescence measurement, comprising the steps of:

selecting a plurality of pixel regions on a detector, each of said plurality of pixel regions covering an area on the detector where emission light from a single sample will impinge the detector;

selecting a pixel group size within each pixel region, each pixel group comprising a square of one or more pixels and producing a single reading, each pixel region comprising a plurality of pixel groups;

directing excitation beams of light towards a plurality of samples;

collecting emission light from the plurality of samples with an objective;

directing the collected emission light of each of the plurality of samples as an image on a pixel region on the detector;

detecting, for each image, intensity readings of the plurality of pixel groups comprising the pixel region on the detector corresponding to the image;

determining a spatial distribution of intensity readings for each image; and

determining the integrity of each of the plurality of samples by determining if a spatial distribution of intensity readings of an image of said each sample is uniform within its respective pixel region, wherein a uniform distribution indicates a sample with integrity;

wherein the pixel group size is chosen so that a non-uniform distribution will be detected.