Polymeric nucleic acid hybridization probes

• US 20050112636A1
• Filed: 09/23/2004
• Published: 05/26/2005
• Est. Priority Date: 09/23/2003
• Status: Abandoned Application

• Current Assignee: ATOM Sciences Corporation
• Original Assignee: ATOM Sciences Corporation
• Inventors: Whitaker, Tom J., Hurt, Richard A.
• Application Number:
  US10/947,310
• Publication Number:
  US 20050112636A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6832 Enhancement of hybridisation reaction
• CPC Class Codes: C12Q 2525/151 repeat or repeated sequences, e.g. VNTR, microsatellite, concatemer
• CPC Class Codes: C12Q 2537/143 Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
• CPC Class Codes: C12Q 2565/543 characterised by the use of two or more capture oligonucleotide primers in concert, e.g. bridge amplification

Abstract

A novel polymeric nucleic acid probe improves detection sensitivity and specificity in a variety of hybridization platforms. The probe is made up of multiple short nucleic acid sequences (referred to as monomers) attached together to form a long polymeric probe for use in hybridization applications. For applications requiring immobilization of the probes to a surface, the polymeric probes are similar to long DNA probes in that they can be immobilized to a variety of surfaces without need for a chemical modification to the end of the probe. Because target nucleic acids hybridize to the relatively short monomers in the polymeric probe, the polymeric probes are more specific than long DNA probes. In addition, polymeric probes also improve the signal-to-background ratio by increasing the number of accessible monomer oligonucleotide probes immobilized per unit area on a surface.

Claims

1. A single-stranded polymeric probe comprising multiple copies of one or more sequences of single-stranded nucleic acid (monomers), which are joined together, wherein;

the monomers are at least 6 nucleotides in length;

the monomers are joined either directly end-to-end or to opposite ends of a molecular linker that may or may not include other monomers with a different sequence;

said polymeric probe contains at least 4 copies of said monomer; and

said polymeric probe has at least one probe sequence that is known to be complementary either to a potential sequence in a target nucleic acid, to a positive control sequence in the nucleic acid, or to a negative control sequence that is absent in the target nucleic acid.

2. The polymeric probe of claim 1, wherein the monomeric nucleic acid is selected from the group consisting of synthetic oligodeoxynucleotides (ODNs), peptide nucleic acid (PNAs), locked nucleic acids (LNAs), and sections of isolated DNA formed using DNA amplification techniques.

3. The polymeric probe of claim 1 wherein said monomeric sequences of single-stranded nucleic acid include an additional sequence of nucleic acid on one or both ends of said probe sequence.

4. The polymeric probe of claim 1 wherein said monomeric sequences of single-stranded nucleic acid are linked on one or both ends of said probe sequence by a molecular linker that is not a nucleic acid.

5. The polymeric probe of claim 1 wherein the polymeric probe is a homopolymer.

6. The polymeric probe of claim 1 wherein the polymeric probe is a copolymer having two or more different sequences for the monomeric units.

7. The polymeric probe of claim 1 wherein said polymeric probe is linear.

8. The polymeric probe of claim 1 wherein said probe polymeric probe is circular.

9. A method of forming the probe of claim 1 which comprises repeatedly joining a phosphorylated 5′

terminus of a monomer or polymer to a 3′

end of a polymer or monomer sequence that is not phosphorylated on the 5′

end.

10. The process of claim 9 wherein joining is accomplished by hybridizing a complementary coupler nucleic acid to a sequence on the 3′

of one monomer or polymer and to a sequence on the 5′

end of another monomer or polymer, so as to form a double-stranded section with a gap (“

nick”

), and ligating the ends of the nucleic acids that form the gap.

11. The method of claim 10, wherein a ligase enzyme is used to ligate the ends of the nucleic acid.

12. The method of claim 11, wherein the ligase enzyme is an enzyme that requires a phosphate on the 5′

terminus and a hydroxyl on the 3′

terminus of the nucleic acid.

13. The method of claim 12, wherein the ligase enzyme is T4 DNA ligase, T7 DNA ligase, Tfi DNA ligase, Ampligase, Tsc DNA ligase, or Chlorella virus PBCV-1 DNA ligase.

14. The method of claim 10, wherein a universal coupler is used for different probe sequences by terminating the 3′

ends and 5′

ends of the probe sequences with a nucleic acid linker having at least 4 bases in length;

wherein the nucleic acid linker for the 5′

end is the same or different in length, sequence, or both from nucleic acid linker for the 3′

end.

15. The method of claim 10, wherein the ligation is repeated by using a thermal cycle, having a reaction mixture temperature that cycles from a value that permits the coupler to hybridize, to a value that permits ligation, to a value that dissociates the hybridized coupler molecule from the ligated polymer.

16. The method of claim 15, wherein said thermal cycle is repeated multiple times to increase the length of the polymer.

17. The method of claim 15, wherein ligase denaturing is avoided by using a coupler that has a length and G+C content that to will form a hybrid that will dissociate at a temperature where at least 50% of the ligase remains effective after 30 minutes of incubation.

18. The method of claim 15, wherein ligase denaturing is avoided by using a thermally stable ligase.

19. The method of claim 9, wherein the monomers and/or polymers are joined using a ligase that can directly link the single-stranded monomers and polymers together without the need of a coupler molecule.

20. The method of claim 19, wherein the ligase enzyme is T4 RNA ligase or Thermophage™

single-stranded DNA ligase.

21. The method of claim 9, wherein the monomers and/or polymers are joined using a non-ligase enzyme method.

22. A method of making a nucleic acid array, which comprises immobilizing the polymeric probes of claim 1 onto a solid substrate surface at different discrete locations, wherein each polymeric nucleic acid probe is made up of one or more monomer sequences.

23. The method of claim 22, wherein the solid substrate is glass, silicon, nylon, polyacrylamide gel, Teflon™

, or metal.

24. The method of claim 22, wherein the solid substrate surface is coated with a moiety to enhance nucleic acid immobilization.

25. The method of claim 22, wherein the solid substrate surface is coated with an epoxide, aldehyde, poly-L-lysine, nylon, amino, carboxylate, or other moiety that enhances binding chemistry.

26. The method of claim 22 wherein the probes are covalently cross-linked to the solid substrate surface using ultraviolet light, heat, or reactive chemistry.

27. A nucleic acid array comprising polymeric probes of claim 1 immobilized onto a solid substrate surface at different discrete locations, wherein each polymeric nucleic acid probe is made up of one or more monomer sequences.

28. A method of assaying for a target nucleic acid which comprises, contacting a sample that contains the target nucleic acid with a nucleic acid array of claim 27, hybridizing the immobilized polymeric probes with the target nucleic acid;

and detecting hybridization between the polymeric probes and target nucleic acid.

29. The method of claim 28, wherein the detection is done using radiological labeling, fluorescent labeling, bioluminescent labeling, chemiluminescent labeling, electrical detection, or mass spectrometry of labeled or unlabeled target nucleic acid.

30. The method of claim 28, wherein hybridization information obtained from the assay is used to determine if a specific nucleic acid sequence exists in the sample.

31. The method of claim 28, wherein hybridization information obtained from the assay is used to detect nucleic acid polymorphisms.

32. The method of claim 28, wherein the hybridization information from the assay is used to detect and/or identify a pathogen.

33. The method of claim 32, wherein the pathogen is from a bacteria, virus or fungus.

34. The method of claim 28, wherein the hybridization information is used to diagnose a disease.

35. The method of claim 28, wherein the hybridization information is used to monitor the efficacy of a disease treatment.

36. A method of forming a polymeric probe of claim 1, wherein the polymeric probe is prepared by direct oligonucleotide synthesis.

37. A method of forming a polymeric probe of claim 1, wherein the polymeric probe is prepared by strand displacement amplification of a circularized template.

38. The polymeric probe of claim 2, wherein the sections of isolated DNA formed using DNA amplification techniques is formed using polymerase chain reaction (PCR).