Labeling nucleic acids

• US 5,700,921 A
• Filed: 11/27/1995
• Issued: 12/23/1997
• Est. Priority Date: 11/27/1995
• Status: Expired due to Fees

• Current Assignee: Vector Laboratories
• Original Assignee: Vector Laboratories
• Inventors: Westling, Mark E., Daniel, Steven G.
• Primary Examiner(s): Jones, W. Gary
• Assistant Examiner(s): WHISENANT, ETHAN C
• Application Number:
  US08/562,650
• Time in Patent Office: 757 Days
• Field of Search: 536/22.1, 536/25.32, 436/6
• US Class Current: 536/22.1
• CPC Class Codes: C07H 21/00 Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids

Abstract

Reagents and methods for multi-step labeling of nucleic acids allow the addition of relatively insoluble or unstable labels to nucleic acid in the final step. Nucleic acids can be stored as a stable intermediate capable of reacting with a label conjugated to a thiol-reactive group.

Claims

1. A method for modifying a nucleic acid comprising:

a. contacting a nucleic acid with a pro-thiol aryl azide having the structure;

##STR40## and salts thereof wherein, R₁ to R₄, which may be the same or different, are selected from the group consisting of H, alkyl, nitro, hydroxy, halide, carboxylic acid, methoxy, cyano, and amino groups;

wherein E is a chain of C₁ -C₂₀ having chain constituents selected from the group consisting of alkyl, alkenyl, alkynyl and heteroatoms, said chain constituents having substituents selected from the group consisting of H, C₁ -C₆ alkyl, aryl, ester, ether, amine, amide and halo groups; and

wherein Y is a protecting group for protecting the sulfur moiety from chemical reaction and is removable so as to generate a thiol moiety; and

b. subjecting the nucleic acid and the pro-thiol aryl azide to activation conditions sufficient to cause reaction therebetween resulting in modifying the nucleic acid.

2. The method of claim 1 wherein step b comprises photoactivating the pro-thiol aryl azide in the presence of the nucleic acid.

3. The method of claim 2 further comprising:

c. removing unreacted pro-thiol aryl azide; and

d. removing the protecting group Y to form an intermediate having the structure;

##STR41##

4. The method of claim 3 further comprising reacting the intermediate formed in step (d) with a label conjugated to a thiol-reactive group whereby a labeled nucleic acid results having the structure:

##STR42## wherein R₉ is the thiolated conjugate of the thiol-reactive group and L is selected from the group consisting of a ligand or a detectable label.

5. The method of claim 4 wherein L is selected from the group consisting of fluorophores, biotin, fucose and haptens.

6. The method of claim 4 wherein the thiol-reactive group is selected from the group consisting of maleimides, iodoacetamides, pyridyl disulfides, vinyl pyridines, vinyl sulfones, acrylates, aryl mercurial compounds and aziridino compounds covalently linked to the detectable label or ligand.

7. The method of claim 6 wherein the thiol-reactive group is a maleimide and L is fluorescein.

8. A labeling kit for labeling a nucleic acid comprising:

a) a pro-thiol aryl azide having the structure;

##STR43## and salts thereof, wherein, R₁ to R₄, which may be the same or different, are selected from the group consisting of H, alkyl, nitro, hydroxy, halide, carboxylic acid, methoxy, cyano, amino groups;

wherein E is a chain of C₁ -C₂₀ having chain constituents selected from the group consisting of alkyl, alkenyl, alkynyl and heteroatoms, said chain constituents having substituents selected from the group consisting of H, C₁ -C₆ alkyl, aryl, ester, ether, amine, amide and halo groups; and

wherein Y is a group capable of protecting the sulfur moiety from chemical reaction and removable so as to generate a thiol moiety

b) a reagent to remove the protecting group so as to generate a terminal thiol; and

c) a thiol-reactive label or ligand capable of reacting with the thiol.

9. The labeling kit of claim 8 wherein the pro-thiol aryl azide has the structure:

##STR44##