IP Library Granted Patent US 7,863,431
Granted Patent B2
US 7,863,431 · App. 10/763,102 · Granted Jan 4, 2011

Label target and labeling reagents comprising rigid group backbones

Assignee: Enzo Life Sciences, Inc.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,863,431
App. No.
10/763,102
Granted
Jan 4, 2011
Kind
B2
Abstract

This invention provides for labeling reagents, labeled targets and processes for preparing labeling reagents. The labeling reagents can take the form of cyanine dyes, xanthene dyes, porphyrin dyes, coumarin dyes or composite dyes. These labeling reagents are useful for labeling probes or targets, including nucleic acids and proteins. These reagents can be usefully applied to protein and nucleic acid probe based assays. They are also applicable to real-time detection processes.

Claims (87)

1. A labeled target comprising

T-L-M

wherein T is a target, M is a marker moiety and L is a chemical group covalently linking said M to T, said chemical group L comprising a backbone that comprises at least one rigid group that comprises one or more of:

(d) multimers of (a), (b) or (c), and (e) any combinations of (a), (b), (c) and (d).

2. The labeled target of claim 1 , wherein said target T comprises a protein, a peptide, a nucleic acid, a nucleotide or a nucleotide analog, a receptor, a natural or synthetic drug, a synthetic oligomer, a synthetic polymer, a hormone, a lymphokine, a cytokine, a toxin, a ligand, an antigen, a hapten, an antibody, a carbohydrate, a sugar or an oligo- or polysaccharide.

3. The labeled target of claim 2 , wherein said nucleic acid or nucleotide or nucleotide analog is modified.

4. The labeled target of claim 2 , wherein said ligand comprises biotin, iminobiotin, digoxygenin or fluorescein.

5. The labeled target of claim 1 , wherein said marker moiety M comprises a ligand that comprises biotin, iminobiotin, digoxygenin or fluorescein.

6. The labeled target of claim 1 , wherein said marker moiety M comprises a fluorescent dye.

7. The labeled target of claim 6 , wherein said fluorescent dye comprises a xanthene dye, a cyanine dye, a coumarin dye, a porphyrin dye or a composite dye.

8. The labeled target of claim 7 , wherein said xanthene dye comprises fluorescein, rhodamine or rhodol, or derivatives thereof.

9. The labeled target of claim 1 , wherein said backbone comprises one or more carbon atoms.

10. The labeled target of claim 1 , wherein said backbone comprises at least one non-carbon atom.

11. The labeled target of claim 10 , wherein said non-carbon atom comprises sulfur, oxygen or nitrogen.

12. The labeled target of claim 1 , wherein said chemical group L further comprises at least one additional moiety comprising peptide bonds, amino acids, aliphatic chains from C 1 through C 20 , alkene groups, alkyne groups, saturated or unsaturated or partially saturated rings, heterocyclic rings and sugars.

13. The labeled target of claim 1 , wherein said structure (a) comprises two alkene groups in cis conformation to each other.

14. The labeled target of claim 1 , wherein said structure (a) comprises two alkene groups in trans conformation to each other.

15. The labeling reagent of claim 1 , wherein one or more hydrogens are substituted by a chemical moiety.

16. A labeling reagent comprising

R-L-M

wherein R is a reactive group, M is a marker moiety and L is a chemical group covalently linking said M to R, said chemical group L comprising a backbone that comprises at least one rigid group that comprises one or more of:

(d) multimers of (a), (b) or (c),

and (e) any combinations of (a), (b), (c) and (d).

17. The labeling reagent of claim 16 , wherein said reactive group R comprises sulfhydryl, hydroxyl, amine, isothiocyanate, isocyanate, monochlorotriazine, dichlorotriazine, mono- or di-halogen substituted pyridine, mono- or di-halogen substituted diazine, maleimide, aziridine, sulfonylhalide, acid halide, hydroxysuccinimide ester, hydroxysulfosuccinimide ester, imidoester, hydrazine, azidonitrophenyl, azide, 3-(2-pyridyl dithio)-proprionamide, glyoxal or aldehyde.

18. The labeling reagent of claim 17 , wherein as a reactive group R is capable of forming a carbon-carbon linkage with a target.

19. The labeling reagent of claim 18 , wherein said reactive group R comprises an alkene group, an alkyne group, a halogenated compound or a metallo-organic compound.

20. The labeling reagent of claim 19 , wherein said metallo-organic compound comprises mercury, zinc, copper or platinum.

21. The labeling reagent of claim 19 , wherein said metallo-organic compound comprises an aromatic group, an aromatic heterocyclic group, an alkene group or an alkyne group.

22. The labeling reagent of claim 16 , wherein said marker moiety M comprises a ligand that comprises biotin, iminobiotin, digoxygenin or fluorescein.

23. The labeling reagent of claim 16 , wherein said marker moiety M comprises a fluorescent dye.

24. The labeling reagent of claim 23 , wherein said fluorescent dye comprises a xanthene dye, a cyanine dye, a coumarin dye, a porphyrin dye or a composite dye.

25. The labeling reagent of claim 24 , wherein said xanthene dye comprises fluorescein, rhodamine or rhodol, or derivatives thereof.

26. The labeling reagent of claim 16 , wherein said backbone comprises one or more carbon atoms.

27. The labeling reagent of claim 16 , wherein said backbone comprises at least one non-carbon atom.

28. The labeling reagent of claim 27 , wherein said non-carbon atom comprises sulfur, oxygen or nitrogen.

29. The labeling reagent of claim 27 , wherein said chemical group L further comprises at least one additional moiety comprising peptide bonds, amino acids, aliphatic chains from C 1 through C 20 , alkene groups, alkyne groups, saturated or unsaturated or partially saturated rings, heterocyclic rings and sugars.

30. The labeling reagent of claim 16 , wherein said structure (a) comprises two alkene groups in cis conformation to each other.

31. The labeling reagent of claim 16 , wherein said structure (a) comprises two alkene groups in trans conformation to each other.

32. The labeling reagent of claim 16 , wherein one or more hydrogens are substituted by a chemical moiety.

33. A labeled target comprising

T-L-M

wherein T is a target, M is a marker moiety and L is a chemical group covalently linking said M to T, said chemical group L comprising a backbone that comprises at least two consecutive polar rigid units.

34. The labeled target of claim 33 , wherein said target T comprises a protein, a peptide, a nucleic acid, a nucleotide or a nucleotide analog, a receptor, a natural or synthetic drug, a synthetic oligomer, a synthetic polymer, a hormone, a lymphokine, a cytokine, a toxin, a ligand, an antigen, a hapten, an antibody, a carbohydrate, a sugar or an oligo- or polysaccharide.

35. The labeled target of claim 34 , wherein said nucleic acid or nucleotide or nucleotide analog is modified.

36. The labeled target of claim 34 , wherein said ligand comprises biotin, iminobiotin, digoxygenin or fluorescein.

37. The labeled target of claim 33 , wherein said marker moiety M comprises a ligand that comprises biotin, iminobiotin, digoxygenin or fluorescein.

38. The labeled target of claim 33 , wherein said marker moiety M comprises a fluorescent dye.

39. The labeled target of claim 38 , wherein said fluorescent dye comprises a xanthene dye, a cyanine dye, a coumarin dye, a porphyrin dye or a composite dye.

40. The labeled target of claim 39 , wherein said xanthene dye comprises fluorescein, rhodamine or rhodol, or derivatives thereof.

41. The labeled target of claim 33 , wherein at least one of said two consecutive rigid polar units of said backbone is heteroatomic.

42. The labeled target of claim 41 , wherein said heteroatomic backbone comprises a carbon atom that is bonded to a N, S, O, P or halogen atom.

43. The labeled target of claim 41 , wherein said heteroatom comprises an —OH, —SH, —SO 3 , —PO 4 , —COOH or —NH 2 groups.

44. The labeled target of claim 41 , wherein at least one of said two consecutive rigid polar units comprises a peptide bond.

45. The labeled target of claim 41 , wherein at least one of said two consecutive polar units comprises a ring structure.

46. The labeled target of claim 45 , wherein said ring structure further comprises polar or charged functional groups attached to said ring.

47. The labeled target of claim 46 , wherein said polar or charged functional groups comprise halide, —OH, —SH, —SO 3 , —PO 4 , —COOH or —NH 2 groups.

48. The labeled target of claim 45 , wherein said ring structure comprises a sugar.

49. The labeled target of claim 45 , wherein said ring structure comprises a substituted heterocyclic aromatic compound.

50. The labeled target of claim 33 , wherein said backbone comprises one or more carbon atoms.

51. The labeled target of claim 33 , wherein said backbone comprises at least one non-carbon atom.

52. The labeled target of claim 51 , wherein said non-carbon atom comprises sulfur, oxygen or nitrogen.

53. The labeled target of claim 33 , wherein said chemical group L further comprises at least one additional moiety comprising peptide bonds, amino acids, aliphatic chains from C 1 through C 20 , alkene groups, alkyne groups, saturated or unsaturated or partially saturated rings, heterocyclic rings and sugars.

54. A labeling reagent comprising

R-L-M

wherein R is a reactive group, M is a marker moiety and L is a chemical group covalently linking said M to R, said chemical group L comprising a backbone that comprises at least two consecutive polar rigid units.

55. The labeling reagent of claim 54 , wherein said reactive group R comprises sulfhydryl, hydroxyl, amine, isothiocyanate, isocyanate, monochlorotriazine, dichlorotriazine, mono- or di-halogen substituted pyridine, mono- or di-halogen substituted diazine, maleimide, aziridine, sulfonylhalide, acid halide, hydroxysuccinimide ester, hydroxysulfosuccinimide ester, imidoester, hydrazine, azidonitrophenyl, azide, 3-(2-pyridyl dithio)-proprionamide, glyoxal or aldehyde.

56. The labeling reagent of claim 54 , wherein as a reactive group R is capable of forming a carbon-carbon linkage with a target.

57. The labeling reagent of claim 54 , wherein said reactive group R comprises an alkene group, an alkyne group, a halogenated compound or a metallo-organic compound.

58. The labeling reagent of claim 57 , wherein said metallo-organic compound comprises mercury, zinc, copper or platinum.

59. The labeling reagent of claim 57 , wherein said metallo-organic compound comprises an aromatic group, an aromatic heterocyclic group, an alkene group or an alkyne group.

60. The labeling reagent of claim 54 , wherein said marker moiety M comprises a ligand that comprises biotin, iminobiotin, digoxygenin or fluorescein.

61. The labeling reagent of claim 54 , wherein said marker moiety M comprises a fluorescent dye.

62. The labeling reagent of claim 61 , wherein said fluorescent dye comprises a xanthene dye, a cyanine dye, a coumarin dye, a porphyrin dye or a composite dye.

63. The labeling reagent of claim 62 , wherein said xanthene dye comprises fluorescein, rhodamine or rhodol, or derivatives thereof.

64. The labeled target of claim 54 , wherein at least one of said two consecutive rigid polar units is heteroatomic.

65. The labeled target of claim 64 , wherein said heteroatomic rigid polar units comprises a carbon atom that is bonded to a N, S, O, P or halogen atom.

66. The labeled target of claim 64 , wherein said heteroatom comprises an —OH, —SH, —SO 3 , —PO 4 , —COOH or —NH 2 groups.

67. The labeled target of claim 54 , wherein at least one of said two consecutive rigid polar units comprises a peptide bond.

68. The labeled target of claim 54 , wherein at least one of said two consecutive polar units comprises a ring structure.

69. The labeled target of claim 68 , wherein said ring structure further comprises polar or charged functional groups attached to said ring.

70. The labeled target of claim 69 , wherein said polar or charged functional groups comprise halide, —OH, —SH, —SO 3 , —PO 4 , —COOH or —NH 2 groups.

71. The labeled target of claim 68 , wherein said ring structure comprises a sugar.

72. The labeled target of claim 68 , wherein said ring structure comprises a substituted heterocyclic aromatic compound.

73. The labeling reagent of claim 54 , wherein said backbone comprises one or more carbon atoms.

74. The labeling reagent of claim 54 , wherein said backbone comprises at least one non-carbon atom.

75. The labeling reagent of claim 74 , wherein said non-carbon atom comprises sulfur, oxygen or nitrogen.

76. The labeling reagent of claim 54 , wherein said chemical group L further comprises at least one additional moiety comprising peptide bonds, amino acids, aliphatic chains from C 1 through C 20 , alkene groups, alkyne groups, saturated or unsaturated or partially saturated rings, heterocyclic rings and sugars.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2026
From: ENZO BIOCHEM, INC.; ENZO LIFE SCIENCES, INC.; ENZO THERAPEUTICS, INC.
To: SERAPH BIOTECH CONSULTING, LLC
Reel/Frame 075219/0465 →
RELEASE OF SECURITY INTEREST Recorded Jul 24, 2023
From: GEMINO HEALTHCARE FINANCE, LLC D/B/A SLR HEALTHCARE ABL
To: ENZO BIOCHEM, INC.; ENZO CLINICAL LABS, INC.; ENZO LIFE SCIENCES U.S. HOLDING CORP; ENZO LIFE SCIENCES, INC.
Reel/Frame 064369/0031 →
SECURITY INTEREST Recorded Apr 3, 2023
From: ENZO LIFE SCIENCES, INC.; ENZO CLINICAL LABS, INC.; ENZO BIOCHEM, INC.; ENZO LIFE SCIENCES U.S. HOLDING CORP
To: GEMINO HEALTHCARE FINANCE, LLC D/B/A SLR HEALTHCARE ABL
Reel/Frame 063239/0103 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2015
From: STAVRIANOPOULOS, JANNIS G.; RABBANI, ELAZAR
To: ENZO LIFE SCIENCES, INC.
Reel/Frame 036771/0058 →
Continuity (2)
Division 1009607500 · Mar 12, 2002
Related Publication 20090069500A1 · Mar 12, 2009