Cleavable linkers for polynucleotides

• US 7,572,908 B2
• Filed: 03/23/2006
• Issued: 08/11/2009
• Est. Priority Date: 03/23/2006
• Status: Active Grant

• Current Assignee: Agilent Technologies, Inc., The Board of Regents of the University of Colorado (University of Colorado System)
• Original Assignee: Agilent Technologies, Inc., The Board of Regents of the University of Colorado (University of Colorado System)
• Inventors: Dellinger, Douglas J, Caruthers, Marvin, Myerson, Joel, Dellinger, Geraldine, Timar, Zoltan
• Primary Examiner(s): Lewis; Patrick T
• Application Number:
  US11/389,388
• Publication Number:
  US 20070224603A1
• Time in Patent Office: 1,237 Days
• Field of Search: None
• US Class Current: 536/25.3
• CPC Class Codes: C07H 21/04 with deoxyribosyl as saccharide radical

Abstract

In various embodiments of the invention, novel compositions having a polynucleotide bound to a substrate via a cleavable linker are provided, and methods of cleaving a polynucleotide from a substrate are provided.

Claims

1. A method comprising:

contacting a polynucleotide bound to a substrate via a cleavable linker with a solution comprising an α

-effect nucleophile to result in cleavage of the polynucleotide from the substrate;

wherein the cleavable linker has a structure selected from structures (I), (II), (III), (IV), or (V);

2. The method of claim 1 wherein the solution is at a pH of about 6 to about 12.

3. The method of claim 1 wherein the α

-effect nucleophile is characterized as having a pKa in the range of about 4 to 13.

4. The method of claim 1 wherein the solution comprising the α

-effect nucleophile is a solution comprising one or more species selected from hydrogen peroxide, a peracid, a perboric acid, an alkylperoxide, a hydroperoxide, a butylhydroperoxide, a benzylhydroperoxide, a phenylhydroperoxide, a cumene hydroperoxide, performic acid, a peracetic acid, perbenzoic acid, a substituted perbenzoic acid, chloroperbenzoic acid, perbutyric acid, tertiary-butylperoxybenzoic acid, decanediperoxoic acid, corresponding salts of said species, and combinations thereof.

5. The method of claim 1 wherein the solution comprising the α

-effect nucleophile is a solution comprising one or more species selected from hydrogen peroxide, salts of hydrogen peroxide, and mixtures of hydrogen peroxide and performic acid.

6. The method of claim 1 wherein the α

-effect nucleophile is formed in situ by a reaction of hydrogen peroxide and a carboxylic acid or carboxylic acid salt.

7. The method of claim 1 wherein the cleavable linker has a structure selected from structures (I) or (II);

wherein R3, R4, R6, R7, R10, and R11 are each independently selected from H or lower alkyl; and

R5 is -Lnk-Sub.

8. The method of claim 1 wherein the cleavable linker has a structure selected from structures (III), (IV) or (V);

wherein R4, R6, R7, R10, and R11 are each independently selected from H or lower alkyl;

R5 is -Lnk-Sub; and

R13 is lower alkyl.

9. The method of claim 1, wherein the linking group Lnk is selected from:

(1) a lower alkyl group;

(2) a modified lower alkyl group in which one or more linkages selected from ether-, thio-, amino-, oxo-, ester-, and amido- is present;

(3) a modified lower alkyl substituted with one or more groups including lower alkyl;

aryl, aralkyl, alkoxyl, thioalkyl, hydroxyl, amino, amido, sulfonyl, halo;

or

(4) a modified lower alkyl substituted with one or more groups including lower alkyl;

alkoxyl, thioalkyl, hydroxyl, amino, amido, sulfonyl, halo, and in which one or more linkages selected from ether-, thio-, amino-, oxo-, ester-, and amido- is present.

10. The method of claim 1, wherein the linking group Lnk has the structure

—

(CH2)m-Lkg-(CH2)n-

wherein;

m and n are integers independently selected from the range of 1 to about 12, and Lkg is a linkage selected from ether-, thio-, amino-, oxo-, ester-, or amido-.

11. The method of claim 1, further comprising recovering the polynucleotide after cleavage of the polynucleotide from the substrate.

12. The method of claim 1, wherein the polynucleotide comprises at least one protecting group selected from a nucleobase protecting group, a 2′

-hydroxyl protecting group, and a phosphate protecting group, wherein said at least one protecting group is labile under conditions which include an α

-effect nucleophile; and

wherein said contacting results in concurrent cleavage of the polynucleotide from the substrate and deprotection of the polynucleotide.

13. The method of claim 1:

wherein the polynucleotide bound to the substrate via the cleavable linker is an RNA, said RNA has a 2′

-hydroxyl protecting group, said 2′

hydroxyl protecting group is characterized as being peroxyanion-labile;

wherein the α

-effect nucleophile is a peroxyanion; and

wherein said contacting results in concurrent cleavage of the RNA from the substrate and cleavage of the 2′

-hydroxyl protecting group.

14. The method of claim 1:

wherein the polynucleotide comprises a 2′

-hydroxyl protecting group and at least one additional protecting group selected from a nucleobase protecting group and a phosphorus protecting group;

wherein said 2′

-hydroxyl protecting group is stable under conditions which include an α

-effect nucleophile;

wherein said at least one additional protecting group is labile under conditions which include an α

-effect nucleophile; and

wherein said contacting results in concurrent cleavage of the polynucleotide from the substrate and cleavage of said at least one additional protecting group.

15. The method of claim 14 further comprising cleaving the 2′

hydroxyl protecting group under conditions sufficient to result in cleavage of the 2′

hydroxyl protecting group, wherein said conditions do not include α

-effect nucleophile.

16. The method of claim 1:

wherein the polynucleotide comprises a 2′

-hydroxyl protecting group, a phosphorus protecting group, and a nucleobase protecting group;

wherein said 2′

-hydroxyl protecting group and said phosphorus protecting group are stable under conditions which include an α

-effect nucleophile;

wherein said nucleobase protecting group is labile under conditions which include an α

-effect nucleophile; and

wherein said contacting results in concurrent cleavage of the polynucleotide from the substrate and cleavage of said nucleobase protecting group.

17. The method of claim 16 further comprising cleaving at least one protecting group selected from the 2′

-hydroxyl protecting group and the phosphorus protecting group under conditions sufficient to result in cleavage of the at least one protecting group, wherein said conditions do not include α

-effect nucleophile.

18. A composition comprising a polynucleotide bound to a substrate via a cleavable linker, wherein the cleavable linker has a structure selected from structures (I), (II), (III), (IV), or (V):

19. The composition of claim 18 wherein the cleavable linker is characterized as being a peroxyanion-labile linker.

20. The composition of claim 18 wherein the cleavable linker has a structure selected from structures (I) or (II);

wherein R3, R4, R6, R7, R10, and R11 are each independently selected from H or lower alkyl; and

R5 is -Lnk-Sub.

21. The composition of claim 18 wherein the cleavable linker has a structure selected from structures (III), (IV) or (V);

wherein R4, R6, R7, R10, and R11 are each independently selected from H or lower alkyl;

R5 is -Lnk-Sub; and

R13 is lower alkyl.

22. The composition of claim 18, wherein the linking group Lnk is selected from:

(1) a lower alkyl group;

(2) a modified lower alkyl group in which one or more linkages selected from ether-, thio-, amino-, oxo-, ester-, and amido- is present;

(3) a modified lower alkyl substituted with one or more groups including lower alkyl;

aryl, aralkyl, alkoxyl, thioalkyl, hydroxyl, amino, amido, sulfonyl, halo;

or

(4) a modified lower alkyl substituted with one or more groups including lower alkyl;

alkoxyl, thioalkyl, hydroxyl, amino, amido, sulfonyl, halo, and in which one or more linkages selected from ether-, thio-, amino-, oxo-, ester-, and amido- is present.

23. The composition of claim 18, wherein the linking group Lnk has the structure

—

(CH2)m-Lkg-(CH2)n-

wherein;

m and n are integers independently selected from the range of 1 to about 12, and

Lkg is a linkage selected from ether-, thio-, amino-, oxo-, ester-, or amido-.

24. The composition of claim 18 wherein the polynucleotide comprises at least one protecting group selected from a nucleobase protecting group, a 2′

-hydroxyl protecting group, and a phosphorus protecting group, wherein said at least one protecting group and the cleavable linker are both characterized as labile under conditions which include an α

-effect nucleophile.

25. The composition of claim 18:

wherein the polynucleotide bound to the substrate via the cleavable linker is an RNA, said RNA has a 2′

-hydroxyl protecting group; and

wherein said 2′

hydroxyl protecting group and the cleavable linker are characterized as being labile under conditions which include an α

-effect nucleophile.

26. The composition of claim 18:

wherein the polynucleotide comprises a 2′

-hydroxyl protecting group and at least one additional protecting group selected from a nucleobase protecting group and a phosphorus protecting group,

wherein said 2′

-hydroxyl protecting group is characterized as stable under conditions which include an α

-effect nucleophile;

wherein said at least one additional protecting group is characterized as labile under conditions which include an α

-effect nucleophile.

27. The composition of claim 18:

wherein the polynucleotide comprises a 2′

-hydroxyl protecting group, a phosphorus protecting group, and a nucleobase protecting group,

wherein said 2′

-hydroxyl protecting group is characterized as stable under conditions which include an α

-effect nucleophile;

wherein said phosphate protecting group is characterized as stable under conditions which include an α

-effect nucleophile; and

wherein said nucleobase protecting group is characterized as labile under conditions which include an α

-effect nucleophile.