Attachment of second harmonic-active moiety to molecules for detection of molecules at interfaces

• US 6,953,694 B2
• Filed: 12/06/2000
• Issued: 10/11/2005
• Est. Priority Date: 12/06/2000
• Status: Expired due to Term

• Current Assignee: Trustees Of Columbia University In The City Of New York (Columbia University)
• Original Assignee: Trustees Of Columbia University In The City Of New York (Columbia University)
• Inventors: Eisenthal, Kenneth B., Salafsky, Joshua S.
• Primary Examiner(s): Le, Long V.
• Assistant Examiner(s): Counts, Gary W.
• Application Number:
  US09/731,366
• Publication Number:
  US 20020094520A1
• Time in Patent Office: 1,770 Days
• Field of Search: 436/501, 436/164, 436/172, 436/505, 436/800, 436/518, 435/5, 435/7.1, 435/6, 435/7.92, 422 8205- 8209, 356/300, 356/318
• US Class Current: 436/164
• CPC Class Codes: G01N 33/5005 involving human or animal cells immunoassay G01N33/56966; immunoassays of protozoa G01N33/56905; protozoa in screening assays C12Q1/025
• CPC Class Codes: G01N 33/533 with fluorescent label
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/583 with non-fluorescent dye label

Abstract

This invention provides methods of detecting molecules at an interface, which comprise labeling the molecules with a second harmonic-active moiety and detecting the labeled molecules at the interface using a surface selective technique. The invention also provides methods for detecting a molecule in a medium and for determining the orientation of a molecular species within a planar surface using a second harmonic-active moiety and a surface selective technique.

Claims

1. A method for detecting a molecule which is labeled with a second harmonic-active label at an interface, which comprises:

(a) contacting the labeled molecule with the interface such that the label has a net orientation at the interface;

(b) detecting light emitted from the interface using a surface selective technique so as to detect the labeled molecule in contact with the interface,

wherein an unlabeled molecule at the interface is undetectable using the surface selective technique, and wherein the second harmonic-active label is hyperpolarizable.

2. The method of claim 1, wherein the surface selective technique is second harmonic generation or sum-frequency generation.

3. The method of claim 1, wherein the molecule is a protein, a nucleic acid, a lipid, or a carbohydrate.

4. The method of claim 3, wherein the nucleic acid is a ribonucleic acid (RNA) or a deoxyribonucleic acid (DNA).

5. The method of claim 1, wherein the molecule is a pollutant.

6. The method of claim 1, wherein the molecule is on a surface of a nanoparticle or a polymer bead.

7. The method of claim 1, wherein the second harmonic-active label is bound to the molecule by a specific interaction or a non-specific interaction.

8. The method of claim 7, wherein the specific interaction comprises a covalent bond or a hydrogen bond.

9. The method of claim 7, wherein the non-specific interaction comprises an electrostatic interaction.

10. The method of claim 1, wherein the second harmonic-active label is specific for an amine group or a sulfhydryl group on the molecule.

11. The method of claim 1, wherein the second harmonic-active label comprises a plurality of individual second harmonic-active moieties which each have a nonlinear hyperpolarizability and are bound together in a fixed and determinate orientation with respect to each other so as to increase the overall nonlinear hyperpolarizability of the second harmonic-active label.

12. The method of claim 1, wherein the interface is at a membrane, a liposome, a cell surface, a viral surface, a bacterial surface, or a biosensor.

13. The method of claim 1, wherein the interface is a vapor-liquid interface, a liquid-liquid interface, a liquid-solid, or a solid-solid interface.

14. The method of claim 13, wherein the vapor-liquid interface is an air-water interface.

15. The method of claim 13, wherein the liquid-liquid interface is an oil-water interface.

16. The method of claim 13, wherein the liquid-solid interface is a water-glass interface or a benzene-SiO₂ interface.

17. The method of claim 1, wherein the molecule is a protein and the interface is at a receptor on a membrane.

18. The method of claim 1, wherein the molecule is on a viral surface and the interface is at a cell surface.

19. The method of claim 1, wherein the molecule is a protein and the interface is at a protein.

20. The method of claim 1, wherein the molecule is on a cell and the interface is at a cell surface.

34. The method of claim 1, wherein the interface is a cell surface and the labeled molecule is prepared outside of the cell.

21. A method for detecting a molecule in a medium, which comprises:

(a) labeling a surface with a first molecule which is labeled with a second harmonic-active label, which is hyperpolarizable and at an interface wherein the first molecule specifically interacts with a second molecule to be detected,

(b) contacting the surface with a medium comprising the second molecule, thereby creating an interface at the surface such that the label has a net orientation at the interface.

(c) detecting the first molecule at the interface by measuring a signal generated by the second harmonic-active label using a surface selective technique, wherein an unlabeled molecule at the interface is undetectable using the surface selective technique, and

(d) detecting a change in the signal when the second molecule interacts with the first molecule, thereby detecting the second molecule in the medium.

22. The method of claim 21, wherein the surface is on a nanoparticle or a polymer bead.

23. The method of claim 21, wherein the surface selective technique is second harmonic generation or sum-frequency generation.

24. The method of claim 21, wherein the molecule is a pollutant or a charged species.

25. The method of claim 24, wherein the pollutant is lead or polychlorinated biphenyl.

26. The method of claim 24, wherein the charged species is a chloride ion.

27. The method of claim 21, wherein the interaction between the second harmonic-active labeled molecule and the molecule to be detected is an antibody-antigen interaction.

28. The method of claim 21, wherein the medium contains an amount of the molecule to be detected, the change in the signal when the molecule interacts with the second harmonic-active labeled molecule is a quantitative change, and the amount of the molecule in the medium is determined from the change in the signal.

29. The method of claim 21, wherein the molecule to be detected is labeled with a second harmonic-active label.

32. The method of claim 21, wherein the first molecule or the second molecule is selected from the group consisting of a lipid, carbohydrate, protein and nucleic acid.

30. A method for detecting an interaction between a first molecule which is labeled with a second harmonic-active label and a second molecule, which comprises:

(a) contacting the first molecule at an interface with a medium comprising the second molecule such that the label has a net orientation at the interface wherein the first molecule specifically interacts with the second molecule; and

(b) detecting an interaction between the first molecule and the second molecule at the interface by measuring a signal generated by the second harmonic-active label using a surface selective technique, wherein an unlabeled molecule at the interface is undetectable using the surface selective technique, and wherein the second harmonic-active label is hyperpolarizable.

31. The method of claim 30, wherein said second molecule is labeled with a second harmonic-active label.

33. The method of claim 30, wherein the first molecule or the second molecule is selected from the group consisting of a lipid, carbohydrate, protein and nucleic acid.