Method for base sequencing and biologically active nucleic acids

• US 7,374,882 B2
• Filed: 11/11/2001
• Issued: 05/20/2008
• Est. Priority Date: 11/28/2000
• Status: Expired due to Fees

• Current Assignee: Riken
• Original Assignee: Riken
• Inventors: Hayashizaki, Yoshihide
• Primary Examiner(s): Riley; Jezia
• Application Number:
  US10/432,991
• Publication Number:
  US 20040115665A1
• Time in Patent Office: 2,382 Days
• Field of Search: 435/6, 435/91.1, 435/91.2, 536/23.1, 536/24.3, 536/24.33
• US Class Current: 435/6.11
• CPC Class Codes: C07H 19/10 with the saccharide radical esterified by phosphoric or polyphosphoric acids
• CPC Class Codes: C07H 19/20 with the saccharide radical esterified by phosphoric or polyphosphoric acids
• 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
• CPC Class Codes: C12N 15/115 Aptamers, i.e. nucleic acids binding a target molecule specifically and with high affinity without hybridising therewith ; Nucleic acids binding to non-nucleic acids, e.g. aptamers
• CPC Class Codes: C12N 2310/33 of the base
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 2525/117 incorporating modified base
• 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: G01N 33/6845 Methods of identifying protein-protein interactions in protein mixtures

Abstract

Aptamers are nucleic acids and similar molecules, such as peptide-nucleic acids, that specifically bind to a ligand such as a protein or peptide. The present invention provides aptamers comprising at least one base capable of base pairing and different from the standard Watson-Crick bases. The present invention also relates to a method for preparation of such aptamers and to methods for sequencing nucleic acids that comprise at least one base capable of base pairing and different from the standard Watson-Crick bases.

Claims

1. A method for determining the nucleotide base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases comprising:

a) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C bases;

b) elongating said template using a primer or a promoter or a promoter and an initiator in the presence of a nucleic acid synthesizing enzyme, nucleic acid synthesizing enzyme substrates and nucleic acid enzyme substrate derivatives;

c) determining the base sequence of the template as the reverse complement of the sequence of the elongation product obtained in b), wherein the product of step b) comprises a plurality of polynucleotides and each of said polynucleotides is separated from the others differing in length by a single nucleotide.

2. The method of claim 1 wherein after step a) an annealing reaction between said template and a primer able to hybridize to said template is carried out.

3. The method of claim 2, wherein the nucleic acid template comprises at least one standard W-C base A, C, G, T or U and at least one base capable of base pairing and different from the standard W-C bases.

5. The method of claim 1, wherein the base capable of base pairing and different from the standard W-C bases is selected from the group consisting of:

iso-C;

iso-G;

2,6-diaminopyrimidine;

xanthine;

6-amino-5-substituted pyrazin-2(1H)-one;

1 -methyl-pyrazolo [4,3-d]pyrimidine-5,7(4H,6H)-dione;

5-aza-7-deazaguanine;

6-amino-3-substituted pyrazin-2(1H)-one;

3-amino-1-methylpurin-2-one;

2,4-diamino-5,6-dihydropyryimidine;

2-amino-6-(N,N-dimethylamino)purine;

pyridin-2-one;

3-methyl isocarbostyril;

5-methyl isocarbostyril;

7-propynyl isocarbostyril;

m-xylene;

1,3,4-trimethylbenzene;

2-methylanaphthalene;

1,4-dimethylnaphthalene;

1-methylanaphthalene;

naphthalene;

7-azaindole;

isocarbostyril;

6-methyl-7-asaindole;

3-propynyl-7-azaindole;

imidazopyridine;

pyrrolopyridine and a heterocyclic base having a structural formula of

6. The method of claim 1, wherein the base capable of base pairing and different from the standard W-C bases is isoC and/or isoG.

8. The method of claim 1, wherein the template is DNA, the synthesizing enzyme is DNA-dependent DNA polymerase, the synthesizing enzyme substrate is a plurality of dNTPs and substrate derivatives comprise ddNTPs.

9. The method of claim 8, wherein a dNTP or a ddNTP is labeled.

10. The method of claim 9, wherein the primer or initiator is labeled.

11. The method of claim 9, wherein the label is an isotope, a chromophore or a fluorophore.

4. A method for determining the nucleotide base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases comprising:

a) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C bases;

b) elongating said template using a primer or a promoter or a promoter and an initiator in the presence of a nucleic acid synthesizing enzyme, nucleic acid synthesizing enzyme substrates and nucleic acid enzyme substrate derivatives;

c) determining the base sequence of the template as the reverse complement of the sequence of the elongation product obtained in b),

wherein after step a) an annealing reaction between said template and a primer able to hybridize to said template is carried out,

wherein the nucleic acid template comprises at least one standard W-C base A, C, G, T or U and at least one base capable of base pairing and different from the standard W-C bases, and

wherein the base triphosphates different from the standard W-C bases are present at a different concentration than the standard W-C base triphosphates are present at in the elongation step b).

7. A method for determining the nucleotide base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases comprising:

a) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C bases;

b) elongating said template using a primer or a promoter or a promoter and an initiator in the presence of a nucleic acid synthesizing enzyme, nucleic acid synthesizing enzyme substrates and nucleic acid enzyme substrate derivatives;

c) determining the base sequence of the template as the reverse complement of the sequence of the elongation product obtained in b),

wherein the base capable of base pairing and different from the standard W-C bases is isoC and/or isoG, and

wherein the concentration of isoC and isoG triphosphate is lower than the concentration of the standard base triphosphates in the elongation step b).

12. A method for determining the nucleotide base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases comprising:

a) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C bases;

b) elongating said template using a primer or a promoter or a promoter and an initiator in the presence of a nucleic acid synthesizing enzyme, nucleic acid synthesizing enzyme substrates and nucleic acid enzyme substrate derivatives;

c) determining the base sequence of the template as the reverse complement of the sequence of the elongation product obtained in b),

wherein the template is DNA and the synthesizing enzyme is a DNA-dependent RNA polymerase, the synthesizing enzyme substrate is a plurality of NTPs and substrate derivatives comprise 3′

-dNTPs derivatives.

13. The method of claim 12, wherein a NTP or a 3 ′

-dNTP derivative is labeled.

14. The method of claim 12, wherein the primer or initiator is labeled.

15. The method of claim 13, wherein the label is an isotope, a chromophore or a fluorophore.

16. A method for determining the nucleotide base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases comprising:

a) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C bases;

b) elongating said template using a primer or a promoter or a promoter and an initiator in the presence of a nucleic acid synthesizing enzyme, nucleic acid synthesizing enzyme substrates and nucleic acid enzyme substrate derivatives;

c) determining the base sequence of the template as the reverse complement of the sequence of the elongation product obtained in b),

wherein the template is RNA and the synthesizing enzyme is a RNA-dependent DNA polymerase, the synthesizing enzyme substrate is a plurality of dNTPs and the substrate derivatives comprise ddNTPs.

17. The method of claim 16, wherein a dNTP or a ddNTP is labeled.

18. The method of claim 17, wherein the primer or initiator is labeled.

19. The method of claim 17, wherein the label is an isotope, a chromophore or a fluorophore.

20. A method for determining the nucleotide base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases comprising:

a) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C bases;

b) elongating said template using a primer or a promoter or a promoter and an initiator in the presence of a nucleic acid synthesizing enzyme, nucleic acid synthesizing enzyme substrates and nucleic acid enzyme substrate derivatives;

c) determining the base sequence of the template as the reverse complement of the sequence of the elongation product obtained in b),

wherein the template is RNA and the synthesizing enzyme is a RNA-dependcnt RNA polymerase, the synthesizing enzyme substrate is a plurality of NTPs and the substrate derivatives comprise 3′

-dNTPs derivatives.

21. The method of claim 20, wherein a NTP or a 3′

-dNTP derivative is labeled.

22. The method of claim 20, wherein the primer or initiator is labeled.

23. The method of claim 21, wherein the label is an isotope, a chromophore or a fluorophore.

24. A method for determining the nucleotide base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases comprising:

a) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C bases;

b) labeling one end of said template;

c) chemically degrading said labeled template;

d) determining the length of the products obtained in c, obtaining the sequence of the template as the sequence of the incremental lengths of the products.

25. The method of claim 24, wherein the nucleic acid template comprises at least one standard W-C base and at least one base capable of base pairing and different from the standard W-C bases.

26. The method of claim 24, wherein the base capable of base pairing and different from the standard W-C bases is selected from the group consisting of:

iso-C;

iso-G;

2,6-diaminopyrimidine;

xanthine;

6-amino-5-substituted pyrazin-2(1H)-one;

1-methyl-pyrazolo[4,3-d]pyrimidine-5,7(4H,6H)-dione;

5-aza-7-deazaguanine;

6-amino-3-substituted pyrazin-2(1H)-one;

3-amino-1-methylpurin-2-one;

2,4-diamino-5,6-dihydropyryimidine;

2-amino-6-(N,N-dimethylamino)purine;

pyridin-2-one;

3-methyl isocarbostyril;

5-methyl isocarbostyril;

7-propynyl isocarbostyril;

m-xylene;

1,3,4-trimethylbenzene;

2-methylanaphthalene;

1,4-dimethylnaphthalene;

1-methylanaphthalene;

naphthalene;

7-azaindole;

isocarbostyril;

6-methyl-7-asaindole;

3-propynyl-7-azaindole;

imidazopyridine; and

pyrrolopyridine and having a hetrocyclic base having a structural formula of

27. The method of claim 24, wherein the base capable of base pairing and different from the standard W-C bases is isoC and/or isoG.

28. A method for the determination of the base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases, comprising:

A) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C bases;

B) elongating said template using a primer or a promoter or a promoter and an initiator in the presence of a nucleic acid synthesizing enzyme, nucleic acid synthesizing enzyme substrates and nucleic acid synthesizing enzyme substrate derivatives, to produce a plurality of polynucleotides;

C) separating polynucleolides differing in length by a single polynucleotide and determining the base sequence of the separated polynucleotides using MALDI-TOF-MS analysis.

29. A method for the determining the base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases,:

a) providing a nucleic acid template comprising at least one base capable of base pairing and different from the standard W-C standard bases;

b) carrying out elongation by using a primer, a promoter, or a promoter and initiator in the presence of nucleoside triphosphates whose base comprises at least one base capable of base pairing and different from the standard W-C bases by adding a first nucleoside triphosphate and detecting PPi release and degrading the first nucleoside triphosphate, then adding a second nucleoside triphosphate and detecting PPi and degrading the second nucleoside triphosphate, and repeating the procedure according to the kind of base of the nucleoside triphosphates provided;

c) repeating step b) above according to the template bases number desired to be sequenced;

d) determining the sequence of the template as the sequence of the nucleoside triphosphates added.

30. A method for determining the base sequence of a nucleic acid template comprising at least one base capable of base pairing and different from the standard Watson-Crick (W-C) bases,:

a) providing a plurality of oligonucleotides fixed on a chip, the oligonucleotides comprising at least one base capable of base pairing and different from the standard W-C bases and having overlapping frames displaced by one or two bases;

b) hybridizing the oligonucleotides with a labeled template according to the invention comprising at least one base capable of base pairing and different from the standard W-C bases;

c) detecting the signal of the label;

d) determining the sequence of the template as the set of overlapping oligonucleotides that are labeled.