Sequencing single molecules using surface-enhanced Raman scattering

• US 20080239307A1
• Filed: 03/30/2007
• Published: 10/02/2008
• Est. Priority Date: 03/30/2007
• Status: Abandoned Application

• Current Assignee: Lawrence Livermore National Security LLC (Government of the United States of America)
• Original Assignee: Regents of the University of California (University of California)
• Inventors: Lane, Stephen M., Huser, Thomas R., Hollars, Christopher W., Talley, Chad E.
• Application Number:
  US11/731,418
• Publication Number:
  US 20080239307A1
• Time in Patent Office: Days
• US Class Current: 356/301
• CPC Class Codes: G01J 3/02 Details
• CPC Class Codes: G01J 3/0208 using focussing or collimating elements, e.g. lenses or mirrors; performing aberration correction
• CPC Class Codes: G01J 3/0229 using masks, aperture plates, spatial light modulators or spatial filters, e.g. reflective filters
• CPC Class Codes: G01J 3/0262 Constructional arrangements for removing stray light
• CPC Class Codes: G01J 3/44 Raman spectrometry; Scattering spectrometry ; Fluorescence spectrometry
• CPC Class Codes: G01N 21/658 enhancement Raman, e.g. surface plasmons

Abstract

A surface-enhanced Raman scattering method and apparatus to sequence polymeric biomolecules such as DNA, RNA, or proteins is introduced. The method uses metallic nanostructures such as, for example, spherical or cylindrical Au or Ag nanoparticles having characteristic lengths of 10-100 nm which when illuminated with light of the appropriate wavelength produce resonant oscillations of the conduction electrons (plasmon resonance). Electric field enhancements of 30-1000 near the particle surface resulting from such oscillations increase Raman scattering cross-sections by about 10⁶-10¹⁵ due to the E⁴ dependence of the Raman scattering, wherein the largest enhancements occur in the gap/junction between novel closely spaced structures as disclosed herein.

Claims

1. An apparatus, comprising:

a fluidic channel configured to receive one or more polymeric biomolecules;

one or more preconfigured resonant pole nano-structures disposed therein said fluidic channel;

means optically coupled with said preconfigured resonant pole nano-structures and adjacent said one or more desired polymeric biomolecules for identifying a Raman induced spectra.

2. The apparatus of claim 1, wherein said preconfigured resonant pole nano-structures comprises at least one of:

a monopole, a dipole, a serial dipole, a plurality of dipole pairs, and a quadrapole.

3. The apparatus of claim 2, wherein said preconfigured resonant pole nano-structures comprises a super-position of a plurality of said resonant pole nano-structures.

4. The apparatus of claim 2, wherein said preconfigured resonant pole nano-structures comprise at least one shape selected from:

spherical, rodlike, cubic, triangular, and ellipsoidal.

5. The apparatus of claim 2, wherein said preconfigured resonant pole nano-structures comprise at least one structure selected from:

a nanoshell, a nanoshell having a hole, and a nanoshell with a magnetic interior.

6. The apparatus of claim 1, wherein said Raman induced spectra comprises at least one of:

surface enhanced Raman scattering (SERS), surface enhanced resonance Raman scattering (SERRS), and surface enhanced coherent anti-Stokes Raman spectroscopy (SECARS).

7. The apparatus of claim 6, wherein said Raman induced spectra is induced from at least one optical source comprising a continuous wave (CW) and a solid-state laser.

8. The apparatus of claim 7, wherein said at least one optical source comprises a wavelength of at least 200 nm.

9. The apparatus of claim 7, wherein said at least one optical source comprises a degree of polarization selected from:

linear, elliptical, circular or random polarization so that additional or redundant spectral information can be obtained from said one or more polymeric biomolecules.

10. The apparatus of claim 1, wherein said fluidic channel comprises one or more microfluidic channels having an opening from about 0.1 nm to about 5 nm to pass respective said one or more polymeric biomolecules.

11. The apparatus of claim 1, wherein said means comprises at least one detector selected from:

a photodiode, a spectrometer, a monochrometer, a charge coupled device (CCD), and a photomultiplier.

12. The apparatus of claim 1, wherein said apparatus further comprises a computer configured with a processing software.

13. The apparatus of claim 1, wherein said one or more polymeric biomolecules are directed therethrough said fluidic channel via a directional fluid flow.

14. The apparatus of claim 1, wherein said one or more polymeric biomolecules are directed therethrough said fluidic channel via electrophoresis.

15. The apparatus of claim 1, wherein one end of said one or more polymeric biomolecules comprises a coupled dielectric bead, said dielectric bead immobilized by way of an optical trap.

16. The apparatus of claim 1, wherein one end of said one or more polymeric biomolecules comprises a coupled magnetic bead, said magnetic bead immobilized by way of an applied magnetic field.

17. The apparatus according to claims 15 or 16, wherein one or more nucleotides are removed from the unattached end of said one or more polymeric biomolecules by an exonuclease so that said one or more removed nucleotides can be identified via a respective said Raman induced spectra.

22. The apparatus of claim 1, wherein said resonant pole nano-structures are coupled to said one or more polymeric biomolecules by way of a polymerase which carries said resonant pole nano-structures along said one or more polymeric biomolecules to enable sequencing.

18. The apparatus of 1, wherein both ends of said one or more polymeric biomolecules comprises a dielectric coupled bead, wherein said dielectric coupled beads are manipulated by a dual-optical trap so that said one or more polymeric biomolecules can be immobilized and stretched.

20. The apparatus according to claims 18 or 19, wherein said resonant pole nano-structure is adapted as a read-head and configured to scan along the length of said stretched one or more polymeric biomolecules to enable sequencing.

21. The apparatus of according to claims 18 or 19, wherein said read head is fixed and said stretched one or more polymeric biomolecules is directed along said read head to enable sequencing.

19. The apparatus of 1, wherein both ends of said one or more polymeric biomolecules comprises a magnetic coupled bead, wherein said magnetic coupled beads are manipulated by a magnetic field so that said one or more polymeric biomolecules can be immobilized and stretched.

23. An apparatus, comprising:

a fluidic channel configured to receive one or more polymeric biomolecules;

one or more preconfigured wedged resonant nano-structures disposed therein said fluidic channel; and

means optically coupled with said wedged resonant structure and adjacent said one or more desired polymeric biomolecules for identifying a Raman induced spectra.

24. The apparatus of claim 23, wherein said Raman induced spectra comprises at least one of:

surface enhanced Raman scattering (SERS), surface enhanced resonance Raman scattering (SERRS), and surface enhanced coherent anti-Stokes Raman spectroscopy (SECARS).

25. The apparatus of claim 23, wherein said Raman induced spectra is induced from at least one optical source comprising a continuous wave (CW) and a solid-state laser.

26. The apparatus of claim 25, wherein said at least one optical source comprises a wavelength of at least 200 nm.

27. The apparatus of claim 25, wherein said at least one optical source comprises a degree of polarization selected from:

linear, elliptical, circular or random polarization so that additional or redundant spectral information can be obtained from said one or more polymeric biomolecules.

28. The apparatus of claim 23, wherein said fluidic channel comprises one or more microfluidic channels having an opening from about 0.1 nm to about 5 nm to pass respective said one or more polymeric biomolecules.

29. The apparatus of claim 23, wherein said one or more polymeric biomolecules are directed therethrough said fluidic channel via a directional fluid flow.

30. The apparatus of claim 23, wherein said one or more polymeric biomolecules are directed therethrough said fluidic channel via electrophoresis.

31. The apparatus of claim 23, wherein said means comprises at least one detector selected from:

a photodiode, a spectrometer, a monochrometer, a charge coupled device (CCD), and a photomultiplier.

32. The apparatus of claim 23, wherein said apparatus further comprises a computer configured with a processing software.

39. The method of claim 32, further comprising:

directing said one or more molecules therethrough said fluidic channel via a directional fluid flow.

33. A sequencing method, comprising:

directing one or more polymeric biomolecules therethrough a fluidic channel;

sequentially probing the nucleotides along said one or more polymeric biomolecules by way of preconfigured resonant pole nano-structures; and

optically identifying said probed nucleotides by way of Raman induced spectra.

34. The method of claim 33, wherein said preconfigured resonant pole nano-structures comprises at least one of:

a monopole, a dipole, a serial dipole, a plurality of dipole pairs, and a quadrapole.

35. The method of claim 33, wherein said preconfigured resonant pole nano-structures comprise at least one shape selected from:

spherical, rodlike, cubic, triangular, and ellipsoidal.

36. The method of claim 33, wherein said preconfigured resonant pole nano-structures comprise at least one structure selected from:

a nanoshell, a nanoshell having a hole, and a nanoshell with a magnetic interior.

37. The method of claim 33, wherein said Raman induced spectra comprises at least one of:

surface enhanced Raman scattering (SERS), surface enhanced resonance Raman scattering (SERRS), and surface enhanced coherent anti-Stokes Raman spectroscopy (SECARS).

38. The method of claim 33, wherein said one or more polymeric biomolecules comprise at least one molecule selected from:

synthetic nucleotide analogs, proteins, chromosomal DNA, mitochondrial DNA, single-stranded DNA, double-stranded DNA, triple stranded DNA, ribosomal RNA, transfer RNA, heterogeneous nuclear RNA, and messenger RNA.

40. The method of claim 33, further comprising directing said one or more molecules therethrough said fluidic channel via electrophoresis.

41. The method of claim 33, further comprising:

coupling one end of said one or more polymeric biomolecules to a dielectric bead, said dielectric bead immobilized by way of an optical trap.

42. The method of claim 33, further comprising:

coupling one end of said one or more polymeric biomolecules to a magnetic bead, said magnetic bead immobilized by way of an applied magnetic field.

43. The method according to claims 41 or 42, further comprising:

removing one or more nucleotides from the unattached end of said one or more polymeric molecules by an exonuclease so that said one or more removed nucleotides can be identified via a respective said Raman induced spectra.

44. The method of claim 33, further comprising:

coupling both ends of said one or more polymeric molecules comprises to a dielectric bead, wherein said dielectric coupled beads are manipulated by a dual-optical trap so that said one or more polymeric molecules can be immobilized and stretched.

45. The method of claim 33, further comprising:

coupling both ends of said one or more polymeric molecules comprises to a magnetic coupled bead, wherein said magnetic coupled beads are manipulated by a magnetic field so that said one or more polymeric molecules can be immobilized and stretched.

46. The method according to claims 44 or 45, further comprising:

adapting said resonant pole nano-structure as a read-head to scan along the length of said stretched one or more polymeric molecules to enable sequencing.

47. The method according to claims 44 or 45, further comprising:

fixing said read head and directing said stretched one or more polymeric molecules along said read head to enable sequencing.

48. The method of claim 33, further comprising:

coupling said resonant pole nano-structures to a polymerase which carries said resonant pole nano-structures along said one or more polymeric molecules to enable sequencing.

49. The method of claim 33, further comprising:

adapting said fluidic channel with one or more microfluidic channels having respective openings from about 0.1 nm to about 5 nm to pass said one or more polymeric biomolecules.

50. A sequencing method, comprising:

directing one or more polymeric biomolecules therethrough a fluidic channel;

sequentially probing the nucleotides along said one or more polymeric biomolecules by way of one or more preconfigured wedged nano-structures; and

optically identifying said probed nucleotides by way of Raman induced spectra.

51. The method of claim 50, wherein said Raman induced spectra comprises at least one of:

surface enhanced Raman scattering (SERS), surface enhanced resonance Raman scattering (SERRS), and surface enhanced coherent anti-Stokes Raman spectroscopy (SECARS).

52. The method of claim 50, wherein said one or more polymeric biomolecules comprise at least one molecule selected from:

synthetic nucleotide analogs, proteins, chromosomal DNA, mitochondrial DNA, single-stranded DNA, double-stranded DNA, triple stranded DNA, ribosomal RNA, transfer RNA, heterogeneous nuclear RNA, and messenger RNA.

53. The method of claim 50, further comprising:

directing said one or more molecules therethrough said fluidic channel via a directional fluid flow.

54. The method of claim 50, further comprising directing said one or more molecules therethrough said fluidic channel via electrophoresis.

55. The method of claim 50, further comprising:

adapting said fluidic channel with one or more microfluidic channels having respective openings from about 0.1 nm to about 5 nm to pass said one or more polymeric biomolecules.

56. The method of claim 50, further comprising:

coupling one end of said one or more polymeric biomolecules to a dielectric bead, said dielectric bead immobilized by way of an optical trap.

57. The method of claim 50, further comprising:

coupling one end of said one or more polymeric biomolecules to a magnetic bead, said magnetic bead immobilized by way of an applied magnetic field.

58. The method according to claims 56 or 57, further comprising:

removing one or more nucleotides from the unattached end of said one or more polymeric molecules by an exonuclease so that said one or more removed nucleotides can be directed therebetween said one or more resonant wedged structures so that they can be identified via a respective said Raman induced spectra.