Methods of Using Near Field Optical Forces

• US 20150111199A1
• Filed: 03/15/2013
• Published: 04/23/2015
• Est. Priority Date: 05/14/2012
• Status: Abandoned Application

• Current Assignee: Optofluidics Inc.
• Original Assignee: Optofluidics Inc.
• Inventors: Hart, Robert, Cordovez, Bernardo
• Application Number:
  US14/399,600
• Publication Number:
  US 20150111199A1
• Time in Patent Office: Days
• US Class Current: 435/5
• CPC Class Codes: B82Y 20/00 Nanooptics, e.g. quantum optics or photonic crystals
• CPC Class Codes: G01N 21/01 Arrangements or apparatus for facilitating the optical investigation
• CPC Class Codes: G01N 21/47 Scattering, i.e. diffuse reflection G01N21/25, G01N21/41 take precedence G01N21/55 takes precedence
• CPC Class Codes: G01N 21/59 Transmissivity G01N21/25 takes precedence
• 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 2201/06113 Coherent sources; lasers
• CPC Class Codes: G01N 33/5306 Improving reaction conditions, e.g. reduction of non-specific binding, promotion of specific binding
• CPC Class Codes: G02B 21/32 Micromanipulators structurally combined with microscopes
• CPC Class Codes: G21K 1/006 Manipulation of neutral particles by using radiation pressure, e.g. optical levitation production or acceleration of neutral particles H05H3/00
• CPC Class Codes: Y10T 436/143333 Saccharide [e.g., DNA, etc.]

Abstract

Methods of studying, interrogating, analyzing, and detecting particles, substances, and the like with near field light are described. Methods of identifying binding partners, modulators, inhibitors, and the like of particles, substances, and the like with near field light are described. In certain embodiments, the methods comprise immobilizing or trapping the particle, substance, and the like.

Claims

1. A method of measuring at least one property of a substance comprising:

positioning a substance in the vicinity of near-field light of an optical trap;

directing light from a light source to the substance;

detecting the effect of the light on the substance; and

measuring at least one property of the substance based on the detected effect.

2. The method of claim 1, wherein the effect of the light is selected from the group consisting of light scattered by the substance, light emitted by the substance, and light absorbed by the substance.

3. The method of claim 1, further comprising:

immobilizing the substance at a location using the optical trap, thereby forming a trapped substance.

4. The method of claim 1, wherein the optical trap comprises at least one structure selected from the group consisting of optical fibers, photonic waveguides, slot waveguides, plasmonic tweezers, photonic crystal resonators, ring resonators, toroidal resonators, Whispering Gallery Mode Resonators, and Fabry Perot resonators.

5. The method of claim 1, wherein the substance is a substance selected from the group consisting of a molecule, compound, nucleic acid, peptide, protein, antibody, enzyme, quantum dot, nanotube, particle, virus, bacteria, cell, protein complex, carbohydrate, lipoparticle, vesicle, microparticle, oil droplet, and liposome.

6. The method of claim 1, wherein the at least one property of the substance is a property selected from the group consisting of size, structure, chemical composition, refractive index, electrical impedance, electrical permittivity, mass, density, temperature, diffusion coefficient, shape, protein folding state, solubility, crystallinity, enzymatic activity, binding activity, binding kinetics, and dissociation kinetics.

7. The method of claim 1, wherein the light source is the near-field light of the optical trap.

8. The method of claim 1, wherein the light source is an external light source.

9. The method of claim 2, wherein detecting the scattered light comprises detecting the amount of the scattered light.

10. The method of claim 2, wherein detecting the scattered light comprises detecting the amount and wavelength of the scattered light.

11. The method of claim 2, wherein detecting the amount of scattered light comprises the use of a detector selected from the group consisting of a light scattering detector, spectrometer, Raman spectrometer, photodiode, charged coupled device (CCD), spectrum analyzer, interferometer, ellipsometer, integrating sphere, and photomultiplier.

12. The method of claim 1, wherein measuring the property of the substance comprises measuring the motion of the substance.

13. The method of claim 3, further comprising releasing the trapped substance.

14. A method of measuring the binding activity of a substance comprising;

immobilizing the substance at a location using an optical trap, thereby forming a trapped substance;

contacting the trapped substance with one or more test substances; and

detecting the binding of the strapped substance with one or more test substances.

15. The method of claim 14, wherein the optical trap comprises at least one structure selected from the group consisting of optical fibers, photonic waveguides, slot waveguides, plasmonic tweezers, photonic crystal resonators, ring resonators, toroidal resonators, Whispering Gallery Mode Resonators, and Fabry Perot resonators.

16. The method of claim 14, wherein the trapped substance is a substance selected from the group consisting of a molecule, compound, nucleic acid, peptide, protein, antibody, enzyme, quantum dot, nanotube, particle, virus, bacteria, cell, protein complex, carbohydrate, lipoparticle, vesicle, microparticle, oil droplet, and liposome.

17. The method of claim 14, where in the test substance is a substance selected from the group consisting of a molecule, compound, nucleic acid, peptide, protein, antibody, enzyme, quantum dot, nanotube, particle, virus, bacteria, cell, protein complex, carbohydrate, lipoparticle, vesicle, microparticle, oil droplet, and liposome.

18. The method of claim 14, wherein the method measures the binding kinetics between the trapped substance and the test substance.

19. The method of claim 14, wherein the method measures the binding affinity between the trapped substance and the test substance.

20. The method of claim 14, wherein at least one of the trapped substance and test substance are labeled with a detectable label, and wherein the detecting of binding comprises detecting a detectable signal from the detectable label.

21. The method of claim 14, wherein the detectable label is selected from the group consisting of fluorescent labels, radioactive labels, ferromagnetic labels, paramagnetic labels, luminescent labels, electrochemiluminescent labels, phosphorescent labels, mass labels, Raman labels, molecular beacons, upconverting phosphors and chromatic labels.

22. The method of claim 14, wherein the test substance is contacted with the trapped substance by flowing the test substance to the trapped substance.

23. A method of identifying a modulator of a substance comprising:

immobilizing the substance at a location using an optical trap, thereby forming a trapped substance;

contacting the trapped substance with one or more test substances; and

measuring a property of the trapped substance, wherein a change in the property of the trapped substance when contacted with the test substance indicates that the test substance is a modulator of the substance.

24. The method of claim 23, wherein the optical trap comprises at least one structure selected from the group consisting of optical fibers, photonic waveguides, slot waveguides, plasmonic tweezers, photonic crystal resonators, ring resonators, toroidal resonators, Whispering Gallery Mode Resonators, and Fabry Perot resonators.

25. The method of claim 23, wherein the trapped substance is a substance selected from the group consisting of molecule, compound, nucleic acid, peptide, protein, antibody, enzyme, quantum dot, nanotube, particle, virus, bacteria, cell, protein complex, carbohydrate, lipoparticle, vesicle, microparticle, oil droplet, and liposome.

26. The method of claim 23, wherein the test substance is a substance selected from the group consisting of molecule, compound, nucleic acid, peptide, protein, antibody, enzyme, quantum dot, nanotube, particle, virus, bacteria, cell, protein complex, carbohydrate, lipoparticle, vesicle, microparticle, oil droplet, and liposome.

27. The method of claim 23, wherein the property of the trapped substance is a property selected from the group consisting of size, structure, chemical composition, enzymatic activity, binding activity, binding kinetics, and dissociation kinetics.

28. The methods of claim 23, wherein the test substance is contacted with the trapped substance by flowing the test substance to the trapped substance.

29. A system for measuring a property of a substance comprising:

at least one optical trap; and

at least one detector for measuring the property of the substance.

30. The system of claim 29, further comprising a microfluidic delivery system.

31. The system of claim 29, wherein the at least one optical trap comprises at least one structure selected from the group consisting of optical fibers, photonic waveguides, slot waveguides, plasmonic tweezers, photonic crystal resonators, ring resonators, and toroidal resonators.

32. The system of claim 29, wherein the at least one detector comprises a detector selected from the group consisting of fluorescence microscopes, fluorescence detectors, fluorescence spectrometers, light scattering detectors, optical sensors, Raman microscopes, Raman spectrometers, spectrometers, photodiodes, charged coupled devices (CCDs), Complementary metal-oxide-semiconductor (CMOS) cameras, spectrum analyzers, interferometers, ellipsometers, integrating spheres, and photomultipliers.

33. The system of claim 29, further comprising an external light source.

34. The system of claim 29, wherein the at least one optical trap comprises at least one power source.

35. The system of claim 34, wherein the power source is an optical power source configured to provide optical power to the optical trap.

36. The system of claim 29, further comprising at least one sensor selected from the group consisting of quartz crystal microbalances, cantilevers, electrochemical sensors, acoustic sensors, thermal sensors, impedance sensors, and whispering gallery mode optical sensors.

37. The system of claim 29, wherein the at least one optical trap is patterned on substrate selected from the group consisting of a silicon substrate, glass substrate and polymer substrate.