Detection of biological molecules by differential partitioning of enzyme substrates and products

• US 8,377,686 B2
• Filed: 06/16/2008
• Issued: 02/19/2013
• Est. Priority Date: 09/20/2002
• Status: Active Grant

• Current Assignee: Queen's University At Kingston
• Original Assignee: Queen's University At Kingston
• Inventors: Brown, R. Stephen, Tabash, Samir P., Kozin, Igor S., Marcotte, Eric J. P., Ley, Arthur N., Hall, Kevin R., Hussain, Moe, Hodson, Peter V., Bowers, Raymond J., Wynne-Edwards, Robin A., St. Marseille, John G.
• Primary Examiner(s): BOWERS, NATHAN ANDREW
• Application Number:
  US12/213,207
• Publication Number:
  US 20090117600A1
• Time in Patent Office: 1,709 Days
• Field of Search: 435/288.7, 435/288.1, 435/288.3, 435/287.9, 435/808, 422/82.07, 600/342, 600/317
• US Class Current: 435/288.7
• CPC Class Codes: B82Y 15/00 Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
• CPC Class Codes: C12Q 1/00 Measuring or testing processes involving enzymes, nucleic acids or microorganisms measuring or testing apparatus with condition measuring or sensing means, e.g. colony counters, C12M1/34; Compositions therefor; Processes of preparing such compositions
• CPC Class Codes: C12Q 1/04 Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor C12Q1/6897 takes precedence
• CPC Class Codes: G01N 2021/6484 Optical fibres
• 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 21/6486 Measuring fluorescence of biological material, e.g. DNA, RNA, cells G01N21/6428 takes precedence
• CPC Class Codes: G01N 33/56905 Protozoa
• CPC Class Codes: G01N 33/56911 Bacteria
• CPC Class Codes: G01N 33/56916 Enterobacteria, e.g. shigella, salmonella, klebsiella, serratia
• CPC Class Codes: G01N 33/56983 Viruses
• CPC Class Codes: G01N 33/573 for enzymes or isoenzymes
• CPC Class Codes: Y10S 435/808 Optical sensing apparatus

Abstract

This invention relates to a method and apparatus for detecting a biological molecule associated with enzyme activity in a sample. The invention is applicable to detecting a microorganism associated with an enzyme in a sample such as water, food, soil, or a biological sample. According to a preferred embodiment of the method of the invention, a sample containing an enzyme of interest or a microorganism associated with the enzyme is combined with a suitable substrate, and a fluorescent product of the enzyme-substrate reaction is selectively detected. The fluorescent product is detected with a partitioning element or optical probe/partitioning element of the invention. In one embodiment the partitioning element provides for partitioning of only the fluorescent product molecule into the probe. The invention also provides an automated system for monitoring for biological contamination of water or other samples.

Claims

1. An optical probe for detecting a fluorescent molecule, comprising:

an optical waveguide; and

a partitioning element optically coupled to the optical waveguide;

wherein the fluorescent molecule is selectively partitioned into the partitioning element in accordance with a partition constant (K_fs), such that fluorescence of the fluorescent molecule is coupled into the waveguide.

2. The optical probe of claim 1, wherein the fluorescent molecule is selected from an enzyme substrate and a product of an enzyme-substrate reaction.

3. The optical probe of claim 1, wherein the partitioning element comprises a polymer film.

4. The optical probe of claim 3, wherein the polymer film comprises polydimethylsiloxane (PDMS).

5. The optical probe of claim 1, wherein the optical waveguide is an optical fiber.

6. The optical probe of claim 3, wherein the polymer film comprises a hydrophobic polymer.

7. The optical probe of claim 1, wherein K_fs is greater than one.

8. An apparatus for detecting presence of a fluorescent molecule, comprising:

the optical probe of claim 1;

an excitation light source; and

a detector for detecting fluorescence of the fluorescent molecule;

wherein the detected fluorescence is indicative of presence of the fluorescent molecule.

9. The apparatus of claim 8, wherein the fluorescent molecule is selected from an enzyme substrate and a product of an enzyme-substrate reaction.

10. The apparatus of claim 9, wherein the enzyme is associated with a microorganism.

11. The apparatus of claim 9, wherein the enzyme is selected from β

-glucuronidase and β

-galactosidase.

12. The apparatus of claim 10, wherein the microorganism is selected from Escherichia coli and total coliform bacteria.

13. The apparatus of claim 9, wherein the substrate is selected from pyrene-β

-D-glucuronide, anthracene-β

-D-glucuronide, pyrromethene-β

-D-glucuronide, pyrene-β

-D-galactopyranoside, and anthracene-β

-D-galactopyranoside.

14. A kit for detecting a biological contaminant in a sample, comprising:

the apparatus of claim 8; and

a substrate for an enzyme associated with the biological contaminant;

wherein the fluorescent molecule is the substrate or a product of a reaction of the substrate and the enzyme;

wherein the kit provides an indication of the presence or amount of the biological contaminant in the sample.

15. The kit of claim 14, further comprising a removable vessel for incubating the sample and the substrate.

16. The kit of claim 14, wherein the sample is selected from water, food, a biological sample, and soil.

17. The kit of claim 14, wherein the biological contaminant is at least one microorganism selected from Escherichia coli and total coliform bacteria.

18. The kit of claim 14, wherein the enzyme is at least one enzyme selected from β

-glucuronidase and β

-galactosidase.

19. The kit of claim 14, wherein the substrate is at least one substrate selected from pyrene-β

-D-glucuronide, anthracene-β

-D-glucuronide, pyrromethene-β

-D-glucuronide, pyrene-β

-D-galactopyranoside, and anthracene-β

-D-galactopyranoside.

20. The kit of claim 15, wherein the partitioning element is associated with the vessel.

21. The kit of claim 15, wherein the partitioning element is disposed in the vessel.

22. A method for detecting a fluorescent molecule, comprising:

providing an optical waveguide;

providing a partitioning element optically coupled to the optical waveguide, wherein the fluorescent molecule is selectively partitioned into the partitioning element in accordance with a partition constant (K_fs)such that fluorescence of the fluorescent molecule is coupled into the optical waveguide; and

detecting fluorescence of the fluorescent molecule coupled into the optical waveguide.

23. The method of claim 22, wherein the fluorescent molecule is selected from an enzyme substrate and a product of an enzyme-substrate reaction.

24. The method of claim 22, wherein the partitioning element comprises a polymer film.

25. The method of claim 24, wherein the polymer film comprises a hydrophobic polymer.

26. The method of claim 25, wherein the polymer film comprises polydimethylsiloxane (PDMS).

27. The method of claim 22, further comprising providing an excitation light source that irradiates the fluorescent molecule partitioned into the partitioning element.

28. The method of claim 23, wherein the enzyme is associated with a microorganism.

29. The method of claim 28, wherein the enzyme is selected from β

-glucuronidase and β

-galactosidase.

30. The method of claim 28, wherein the microorganism is selected from Escherichia coli and total coliform bacteria.

31. The method of claim 28, wherein the substrate is selected from pyrene-β

-D-glucuronide, anthracene-β

-D-glucuronide, pyrromethene-β

-D-glucuronide, pyrene-β

-D-galactopyranoside, and anthracene-β

-D-galactopyranoside.

32. The method of claim 22, wherein K_fs is greater than one.