Methods, kits and compositions pertaining to combination oligomers and libraries for their preparation

• US 7,256,275 B2
• Filed: 03/09/2002
• Issued: 08/14/2007
• Est. Priority Date: 03/09/2001
• Status: Expired due to Fees

• Current Assignee: Applied Biosystems LLC (Thermo Fisher Scientific Incorporated)
• Original Assignee: Boston Probes, Inc. (Thermo Fisher Scientific Incorporated)
• Inventors: Coull, James M., Hyldig-Nielsen, Jens J., Fiandaca, Mark J., Kristjanson, Mark D., Creasey, Theresa S.
• Primary Examiner(s): Riley; Jezia
• Application Number:
  US10/096,125
• Publication Number:
  US 20030077608A1
• Time in Patent Office: 1,984 Days
• Field of Search: 435/6, 435/810, 536/23.1, 536/25.3
• US Class Current: 536/23.1
• CPC Class Codes: C07B 2200/11 Compounds covalently bound to a solid support
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 2525/107 incorporating a peptide nucleic acid
• CPC Class Codes: C12Q 2531/113 PCR
• CPC Class Codes: C12Q 2565/137 Chromatographic separation
• CPC Class Codes: C40B 20/04 Identifying library members by means of a tag, label, or other readable or detectable entity associated with the library members, e.g. decoding processes
• CPC Class Codes: C40B 30/04 by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
• CPC Class Codes: C40B 40/00 Libraries per se, e.g. arrays, mixtures
• CPC Class Codes: C40B 40/06 Libraries containing nucleotides or polynucleotides, or derivatives thereof
• CPC Class Codes: Y10S 435/81 Packaged device or kit

Abstract

This invention pertains to the field of combination oligomers, including the block synthesis of combination oligomers in the absence of a template, as well as related methods, kits, libraries and other compositions.

Claims

1. A composition comprising;

(a) a polynucleobase strand; and

(b) a combination oligomer that comprises a first oligomer block and a second oligomer block that are each independently a peptide nucleic acid, PNA chimera or PNA combination oligomer;

wherein the first and second oligomer blocks are linked covalently to each other by a linker that is at least three atoms in length and that is not part of a nucleobase containing backbone subunit of the polymer and the first and second oligomer blocks are sequence specifically hybridized to a target sequence of contiguous nucleobases in the polynucleobase strand to thereby form a double stranded target sequence/combination oligomer complex.

2. The composition of claim 1, which further comprises a third oligomer block that is linked covalently to the first or second oligomer block by a second linker that is at least three atoms in length, such that the second linker is the sane or different in kind from the first said linker.

3. The composition of claim 1, wherein the combination oligomer comprises 6 to 30 nucleobase containing subunits designed to sequence specifically hybridize to a target sequence of contiguous bases in the polynucleobase strand.

4. The composition of claim 1, wherein the first and second oligomer blocks are peptide nucleic acids.

5. The composition of claim 1, wherein the PNA subunits of the oligomer blocks have the formula:

6. The composition of claim 1, wherein the PNA subunits of the oligomer blocks consist of a naturally occurring or non-naturally occurring nucleobase attached to the N-α

-glycine nitrogen of a N-[2-(anilnoethyl)] glycine backbone through a methylene carbonyl linkage.

7. The composition of claim 1, wherein the linker is selected from the group consisting of:

one amino acid residue, two amino acid residues, three amino acid residues, one E-linker residue, two E-Linker residues, one O-linker residue, two O-linker residues, one X-linker residue and two X-linker residues.

8. The composition of claim 7, wherein the linker is selected from the group consisting of:

the amino acid glycine the amino add dimer gly-gly, the amino acid dimer gly-lys. the amino add dimer lys-gly, the amino add dimer glu-gly, the amino add dimer gly-cys, the amino acid dimer cys-gly and the amino add dimer asp-gly.

9. The composition of claim 1, wherein the combination oligomer further comprises at least one energy transfer set of labels such that at least one acceptor moiety of the energy transfer set is linked to one of the linked oligomer blocks of the combination oligomer whilst at least one donor moiety of the energy transfer set is linked to another of the linked oligomer blocks of the combination oligomer wherein the labels of the set are linked to the oligomer blocks at positions that facilitate a change in detectable signal of at least one label when the combination oligomer is hybridized to the target sequence as compared to when the combination oligomer is in a non-hybridized state.

10. The composition of claim 9, wherein the labels of the energy transfer set are linked to the distal-most termini of the oligomer block or to sites within the oligomer blocks.

11. The composition of claim 9, wherein the energy transfer set comprises a single donor moiety and a single acceptor moiety.

12. The composition of claim 11, wherein both the donor and acceptor moieties are fluorophores.

13. The composition of claim 11, wherein the donor moiety is a donor fluorophore and the acceptor moiety is a non-fluorescent quencher moiety.

14. The composition of claim 13, wherein the quencher is a diazo-containing moiety.

15. The composition of claim 1, wherein the combination oligomer further comprises one or more reporter moieties.

16. The composition of claim 15, wherein the one or more reporter moieties are linked at the oligomer block termini, linked at a position internal to the oligomer blocks or linked at a position integral to the linker.

17. The composition of claim 15, wherein the reporter moieties are each independently selected from the group consisting of a chromophore, a fluorochrome, a quencher, a spin label, a radioisotope, an enzyme, a hapten and a chemluminescent compound.

18. The composition of claim 17, wherein the enzyme is selected from the group consisting of alkaline phosphatase, soybean peroxidase, horseradish peroxidase, ribonuclease and protease.

19. The composition of claim 17, wherein the hapten is selected from the group consisting of fluorescein, biotin, 2,4-dinitrophenyl and digoxigenin.

20. The composition of claim 1, wherein the linker comprises a cleavage site for an enzyme.

21. The composition of claim 1, wherein the composition is support bound.

22. The composition of claim 1, wherein the composition exists at a unique position of an array.

23. The composition of claim 1, wherein the target sequence is a subsequence of a polynucleobase strand of nucleic acid that has been amplified by a nucleic acid amplification process.

24. The composition of claim 9, wherein the target sequence is a subsequence of a polynucleobase strand that has been amplified by a nucleic add amplification process.

25. The composition of claim 1, wherein the target sequence is contained within a cell or organism.

26. The composition of claim 1, wherein the target sequence is contained within a polynucleobase strand of nucleic add that has been extracted from a cell or organism.

27. A method comprising:

(a) contacting a palynucleobase strand comprising a target sequence of contiguous nucleobases with a combination oligomer under suitable hybridization conditions;

wherein the combination oligomer comprises a first oligomer block and a second oligomer block tat are each independently a peptide nucleic acid, PNA chimera or PNA combination oligomer;

wherein the first and second oligomer blocks are linked covalently to each other by a linker that is at least three atoms in length and that is not part of a nucleobase containing backbone subunit of the polymer; and

wherein the first and second oligomer blocks are sequence specifically hybridized to the target sequence of contiguous nucleobases to thereby form a double stranded target sequence/combination oligoiner complex; and

(b) determining the complex to thereby determine the target sequence.

28. The method of claim 27, wherein the target sequence is a subsequence of a nucleic add that has been amplified by a nucleic add amplification process.

29. The method of claim 28, wherein the nucleic acid amplification process is selected from the group consisting of:

Polymerase Chain Reaction (PCR), Ligase Chain Reaction (LCR), Strand Displacement Amplification (SDA), Transcription-Mediated Amplification (TMA), Q-beta replicase amplification (Q-beta) and Rolling Circle Amplification (RCA).

30. The method of claim 27, wherein the target sequence is contained within a cell or organism.

31. The method of claim 27, wherein the target sequence is contained within nucleic acid that has been extracted from a cell or organism.

32. The method of claim 27, wherein the combination oligomer further comprises a third oligomer block that Is linked covalently to the first or second oligomer block by a second linker that is at least three atoms in length, such that the second linker is the same or different in kind from the first said linker.

33. The method of claim 27, wherein the combination oligomer comprises 6 to 30 nucleobase containing subunits designed to bind to a target sequence of contiguous nucleobases.

34. The method of claim 27, wherein the first and second oligomer blocks are peptide nucleic adds.

35. The method of claim 27, wherein the PNA subunits of the oligomer blocks of the combination oligomer have the formula:

36. The method of claim 27, wherein the PNA subunits of the oligomer blocks consist of a naturally occurring or non-naturally occurring nucleobase attached to the N-α

-glycine nitrogen of a N-[2-(aminoethyl)] glycine backbone through a methylene carbonyl linkage.

37. The method of claim 27, wherein the linker is selected from the group consisting of:

one amino add residue, two amino acid residues, three amino acid residues, one E-linker residue, two E-Linker residues, one O-linker residue, two O-linker residues, one X-linker residue and two X-linker residues.

38. The method of claim 37, wherein the linker is selected from the group consisting of:

the amino acid glycine, the amino acid dimer gly-gly, the amino acid dimer gly-lys, the amino acid dimer lys-gly, the amino acid dimer glu-gly, the amino add dimer gly-cys, the amino acid dirner cys-gly and the amino acid dimer asp-gly.

39. The method of claim 27, wherein the combination oligomer further comprises at least one energy transfer set of labels such that at least one acceptor moiety of the energy transfer set is linked to one of the linked oligomer blocks of the combination oligomer whilst at Least one donor moiety of the energy transfer set is linked to another of the linked oligomer blocks of the combination oligomer wherein the labels of the set are linked to the oligomer blocks at positions that facilitate a change in detectable signal of at least one label when the combination oligomer is hybridized to the target sequence as compared to when the combination oligomer is in a non-hybridized state.

40. The method of claim 39, wherein the labels of the energy transfer set are linked to the distal-most termini of the oligomer blocks or linked at a position internal to the oligomer blocks.

41. The method of claim 40, wherein the energy transfer set comprises a single donor moiety and a single acceptor moiety.

42. The method of claim 41, wherein both the donor and acceptor moieties are fluorophores.

43. The method of claim 41, wherein the donor moiety is a donor fluorophore and the acceptor moiety is a non-fluorescent quencher moiety.

44. The method of claim 43, wherein the quencher is diazo-containing moiety.

45. The method of claim 27, wherein the combination oligomer further comprises one or more reporter moieties.

46. The method of claim 45, wherein the one or more reporter moieties are linked at the oligomer block termini, linked at a position internal to the oligomer blocks or linked at a position integral to the linker.

47. The method of claim 46, wherein the reporter moieties are selected from the group consisting of:

a chromophore, a fluorochrome, a quencher, a spin label, a radioisotope, an enzyme, a hapten and a chemiluminescent compound.

48. The method of claim 47, wherein the enzyme is selected from the group consisting of alkaline phosphatase, soybean peroxidase, horseradish peroxidase, ribonuclease and protease.

49. The method of claim 47, wherein the hapten is selected from the group consisting of fluorescein, biotin, 2,4-dinitrophenyl and digoxigenin.

50. The method of claim 27, wherein the target sequence is labeled with a reporter moiety.

51. The method of claim 27, wherein neither of the target sequence nor the combination oligomer are labeled with a reporter moiety and the complex is determined using a labeled antibody tat specifically binds to said complex.

52. The method of claim 27, wherein the linker comprises a cleavage site for an enzyme.

53. The method of claim 27, wherein the combination oligomer is support bound.

54. The method of claim 27, wherein the combination oligomer exists at a unique position of an array.

55. A method comprising:

(a) contacting a nucleic acid sample with at least two independently detectable combination oligomers, wherein

(i) each independently detectable combination oligomer comprises a first oligomer block and a second oligomer block that are each independently a peptide nucleic acid, PNA chimera or PNA combination oligomer and are linked covalently to each other by a linker that is at least three atoms in length and that is not part of a nucleobase containing backbone subunit of the polymer; and

(ii) the first and second oligomer blocks taken together encode a probing nucleobase sequence that is designed to sequence specifically hybridize to a target sequence of contiguous nucleobases in a polynucleobase strand of the nucleic add sample to thereby form a double stranded target sequence/independently detectable combination oligomer complex, and the probing nucleobase sequence in each independently detectable combination oligomer differs from the other by at least one nucleobase;

(b) contacting the nucleic acid sample and combination oligomers with one or more reagents suitable for performing a nucleic acid amplification reaction that amplifies the nucleic acid present in the sample;

(c) performing the nucleic add amplification in the presence of the nucleic acid, the combination oligomers and the reagents;

(d) determining complex formation for each independently detectable combination oligomer/target sequence complex to thereby determine whether the nucleic add is heterozygous or homozygous for a particular SNP.

57. The method of claim 55, wherein each independently detectable combination oligomer comprises an independently detectable energy transfer set of labels such tat at least one acceptor moiety of the set is linked to one of the linked oligomer blocks of the combination oligomer whilst at least one donor moiety of the set is linked to another of the linked oligomer blocks of the combination oligomer to thereby produce a change in detectable signal of at least one label when each combination oligomer is sequence specifically hybridized to its target sequence of contiguous nucleobases as compared to when the combination oligomer is in a non-hybridized state.

58. The method of claim 55, wherein the nucleic add amplification reaction is selected from the group consisting of:

Polymerase Chain Reaction (PCR), Ligase Chain Reaction (LCR), Strand Displacement Amplification (SDA), Transcription-Mediated Amplification (TMA), Q-beta replicase amplification (Q-beta) and Rolling Circle Amplification (RCA).

59. The method of claim 57, wherein the nucleic acid amplification reaction is selected from the group consisting of:

Polymerase Chain Reaction (PCR), Ligase Chain Reaction (LCR), Strand Displacement Amplification (SDA), Transcription-Mediated Amplification (TMA), Q-beta replicase amplification (Q-beta) and Rolling Circle Amplification (RCA).

60. The method of claim 55, wherein the first and second oligomer blocks are peptide nucleic acids.

61. The method of claim 57, wherein the first and second oligomer blocks are peptide nucleic acids.

62. The method of claim 57, wherein the labels of each energy transfer set are linked to the distal-most termini of the oligomer blocks or to sites within the oligomer blocks.

63. The method of claim 57, wherein each energy transfer set comprises a single donor moiety and a single acceptor moiety.

64. The method of claim 63, wherein the donor moiety is a donor fluorophore and the acceptor is a non-fluorescent quencher moiety.

65. The method of claim 55, wherein one or more of the target sequence/independently detectable combination oligomer complexes is support bound.

66. The method of claim 57, wherein one or more of the target sequence/independently detectable combination oligomer complexes is support bound.

56. A method comprising:

(a) contacting a combination oligomer with a possible binding partner under suitable binding conditions to thereby possibly form a combination oligomer/binding partner complex;

wherein the combination oligomer is a polymer comprising a segment of the formula;

A-W-C;

 

wherein,

A and C are oligomer blocks that are each independently a pep tide nucleic add, PNA chimera or PNA combination oligomer and are optionally linked to other moieties; and

W is a linker of at least three atoms in length that is not part of a nucleobase containing backbone subunit of the polymer and that;

(i) covalently links oligomer block A to oligomer block C; and

(ii) is a deavage site for an enzyme;

(b) freating the product of step (a) with an enzyme suitable for cleaving the cleavage site under suitable enzyme cleaving conditions; and

(c) determining whether or not the combination oligomer has been cleaved by the activity of the enzyme to thereby determine whether or not the combination oligomer/binding partner complex formed.

67. The method of claim 56, wherein the combination oligomer is a self-indicating combination oligomer comprising an energy transfer set of labels such that at least one acceptor moiety of the energy transfer set is linked to one of the linked oligomer blocks of the combination oligomer whilst at least one donor moiety of the energy transfer set is linked to another of the linked oligomer blocks of the combination oligomer wherein the labels of the set are linked to the oligomer blocks at positions that facilitate a change in detectable signal of at least one label when the combination oligomer is hybridized to a target sequence as compared to when the combination oligomer is in a non-hybridized state.

68. The method of claim 56, wherein the combination oligomer is support bound.