IP Library Granted Patent US 9,598,720
Granted Patent B2
US 9,598,720 · App. 13/971,996 · Granted Mar 21, 2017

Monomeric and polymeric linkers useful for conjugating biological molecules and other substances

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 9,598,720
App. No.
13/971,996
Granted
Mar 21, 2017
Kind
B2
Abstract

The present invention concerns monomeric or polymeric linker molecules useful in biological and chemical applications, their synthesis, and the synthesis and use of derivatives of the linkers conjugated to a variety of detectable labels and other substances. The linkers may be used, for example, in conjunction with fluorescent labels, nucleic acid or nucleic acid analog probes, and solid phase systems, and to enhance the solubility of the conjugated molecules.

Claims (32)

1. A linker derivative comprising at least two consecutive linkers conjugated to at least one atom, functional group, or molecule, wherein each of said at least two consecutive linkers is synthesized from at least one di-carboxylic acid anhydride and at least one diamine wherein the diamine does not comprise more than two —CH2-CH2-O— groups.

2. The linker derivative of claim 1 , wherein at least one of said at least two consecutive linkers is an alternating co-polymer synthesized from the di-carboxylic acid anhydride and the diamine.

3. The linker derivative of claim 1 , wherein the at least one atom, functional group, or molecule comprises at least one detectable label or at least one probe.

4. The linker derivative of claim 3 , wherein the at least one atom, functional group, or molecule comprises at least one detectable label, and wherein the at least one detectable label comprises at least one color label.

5. The linker derivative of claim 4 , wherein the at least one color label comprises at least one fluorophore.

6. The linker derivative of claim 5 , comprising two or more fluorophores of the same or of different and distinguishable emission wavelengths.

7. The linker derivative of claim 1 , comprising at least one nucleic acid or at least one nucleic acid analog.

8. The linker derivative of claim 7 , wherein the at least one nucleic acid analog comprises PNA.

9. The linker derivative of claim 1 , wherein the linker is further attached non-covalently or covalently to at least one solid surface.

10. The linker derivative of claim 9 , wherein the at least one solid surface is dextran.

11. The linker derivative of claim 1 , comprising a detectable label, probe, nucleic acid or nucleic acid analog, and/or solid surface separated from each other by two consecutive linkers, wherein each individual linker comprising between four and ten units chosen from:

wherein R 1 is chosen from and O, R 2 is chosen from NH and O, R 3 is chosen from methyl, ethyl, propyl, CH 2 OCH 2 , and (CH 2 OCH 2 ) 2 , and wherein the linker does not comprise more than three consecutively repeating ethyloxy groups.

12. A method of enhancing the signal intensity, activity, or binding affinity of a molecule, comprising conjugating the molecule to the linker derivative according to claim 11 .

13. The method of claim 12 , wherein the linker comprises at least one unit of the Formula I wherein R 1 and R 2 are NH and R 3 is CH 2 OCH 2 .

14. The method of claim 12 , wherein the linker comprises between three and ten units of Formula I.

15. The method of claim 12 , wherein the molecule comprises at least one detectable label or probe.

16. The method of claim 15 , wherein the molecule comprises at least one detectable label and wherein the at least one detectable label comprises at least one color label.

17. The method of claim 16 , wherein the at least one color label comprises a fluorophore.

18. The method of claim 17 , wherein molecule comprises at least one nucleic acid or nucleic acid analog.

19. The method of claim 18 , wherein the at least one nucleic acid analog comprises PNA.

20. The method of claim 12 , wherein the aqueous solubility of the molecule is enhanced over its solubility in the absence of the linker.

21. A method of amplifying a signal from a change in a molecular system, comprising detecting said change with at least one linker derivative of claim 1 .

22. The method of claim 21 , wherein the linker derivative comprises at least one color label.

23. The method of claim 22 , wherein the at least one color label comprises a fluorophore.

24. A method of claim 21 , wherein the linker derivative comprises at least two fluorophores of the same or of different and distinguishable emission wavelengths, wherein each fluorophore is separated from the other fluorophores of the linker derivative by a linker comprising between four and ten units of the Formula I.

25. A system comprising at least two linker derivatives according to claim 11 , wherein the first linker derivative comprises at least one fluorophore and a nucleic acid or nucleic acid analog, and wherein the second linker derivative comprises a protein or solid surface and a nucleic acid or nucleic acid analog.

26. The system of claim 25 , wherein the nucleic acid analog is PNA.

27. The system of claim 25 , wherein nucleic acid or nucleic acid analogs of the first and second linker derivatives are capable of hybridizing to each other.

28. The system of claim 25 , wherein the first linker derivative is conjugated to at least one fluorophore and to a PNA; wherein the protein or solid surface of the second linker derivative is an antibody, an antigen, and/or dextran, and wherein the PNA of the first linker and second linker derivatives are capable of hybridizing to each other.

29. The system of claim 25 , comprising three linker derivative.

30. The system of claim 26 , comprising three linker derivatives.

31. The system of claim 26 , wherein the first and second linker derivatives are not capable of hybridizing to each other, and wherein the third linker derivative comprises at least one PNA that recognizes PNA sequences on each of the first and second linker derivatives.

Assignments (3)
CHANGE OF NAME Recorded Feb 26, 2020
From: DAKO DENMARK A/S
To: DAKO DENMARK APS
Reel/Frame 052025/0150 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2020
From: DAKO DENMARK APS
To: AGILENT TECHNOLOGIES, INC.
Reel/Frame 052026/0643 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2016
From: LOHSE, JESPER
To: DAKO DENMARK A/S
Reel/Frame 039109/0916 →