Method for Nucleic Acid Analysis

• US 20080287305A1
• Filed: 06/09/2005
• Published: 11/20/2008
• Est. Priority Date: 06/10/2004
• Status: Active Grant

• Current Assignee: Global Life Sciences Solutions USA LLC (Danaher Corporation)
• Original Assignee: GE Healthcare Bio-Sciences Corporation (General Electric Company)
• Inventors: Nelson, John R., Fuller, Carl W.
• Granted Patent: US 7,871,771 B2
• Time in Patent Office: Days
• US Class Current: 506/4
• CPC Class Codes: C12Q 1/6834 Enzymatic or biochemical coupling of nucleic acids to a solid phase
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 2523/113 Denaturating agents
• CPC Class Codes: C12Q 2527/127 the enzyme inhibitor or activator used
• CPC Class Codes: C12Q 2563/137 Metal/ion, e.g. metal label
• CPC Class Codes: C12Q 2565/301 Pyrophosphate (PPi)
• CPC Class Codes: C12Q 2565/519 characterised by the capture moiety being a single stranded oligonucleotide

Abstract

This invention provides methods for nucleic acid analysis. A closed complex of nucleic acid template, nucleotide and polymerase can be formed during polymerase reaction, absent divalent metal ion. This is used to trap the labeled nucleotide complementary to the next template nucleotide in the closed complex. Detection of the label allows determination of the identity of this next correct nucleotide. Identification can be either in place, as part of the complex, or as the dye is eluted from the complex when the reaction cycle is completed by the addition of divalent metal ion. In this way, sequential nucleotides of a DNA can be identified, effectively determining the DNA sequence. This method can be applied to nucleic acid single molecules or to collections of identical or nearly identical sequence such as PCR products or clones. Multiple templates can be sequenced in parallel, particularly if they are immobilized on a solid support.

Claims

1. A method of characterizing a target region of a nucleic acid template, comprising:

a) initiating a nucleic acid polymerization reaction on a support, by forming a reaction mixture, said reaction mixture including a nucleic acid template, a primer, a nucleic acid polymerizing enzyme, and at least one terminal-phosphate-labeled nucleotides each containing a distinct label, wherein a component of said reaction mixture or a first complex of two or more of said components, is immobilized on said support, and said component or components are selected from the group consisting of said nucleic acid template, said primer, and said nucleic acid polymerizing enzyme, and wherein each of said at least one terminal-phosphate-labeled nucleotides contains a base complementary to each of the four naturally occurring bases;

b) progressing said nucleic acid polymerization reaction by incubating said reaction mixture, in the absence of a divalent cation, to form a second complex comprising said nucleic acid template, said primer, said nucleic acid polymerizing enzyme, and a terminal-phosphate-labeled nucleotide, wherein said terminal-phosphate-labeled nucleotide contains a base complementary to the template base at the site of polymerization;

c) removing unbound terminal-phosphate-labeled nucleotides and other components of said reaction mixture; and

d) detecting the label of said terminal-phosphate-labeled nucleotide from said second complex.

2. The method of characterizing a target region of a nucleic acid template of claim 1, further comprising:

e) adding a divalent cation to complete said polymerization reaction;

f) removing said divalent cation and other end products from said polymerization reaction; and

g) repeating steps a) through f) for determining each additional nucleotide sequence.

3. The method of claim 1 or 2, wherein said steps are carried out in a sequential manner in a flow through or a stop-flow system.

4. The method of claim 1 or 2, wherein said support is in the form of beads.

8. The method of claim 1 or 5 wherein said support structure is a first surface of a microscope slide.

9. The method of claim 1 or 5 wherein said labels in said terminal-phosphate-labeled nucleotides are fluorescent dyes or colored dyes.

12. The method of claim 1 or 5, wherein said nucleic acid polymerizing enzyme is FY7 DNA polymerase.

13. The claim of claim 1 or 5, wherein said nucleic acid polymerizing enzyme is selected from DNA polymerase, RNA polymerase, reverse transcriptase, a terminal nucleotidyl transferase, a primase, or a telomerase.

14. The method of claim 1 or 5, wherein said nucleic acid polymerizing enzyme is selected from DNA polymerase I, T4 DNA polymerase, Amplitaq FS, T7 DNA polymerase, Phi 29 DNA polymerase, Klenow exo⁻

, Sequenase, Taq DNA polymerase, Thermo Sequenase I, ThermoSequenase II, FY7 DNA polymerase, ThemoSequenase E681M, T. hypogea (Thy B), T. neapolitana (Tne), T. subterranea (Tsu), T. barossii (Tba), T. litoralis (NEB Vent), T. kodakaraensis (Novagen), P. furiosis (Strategene), P. GB-D (NEB Deep Vent), Human Pol beta, Tsp JS 1, AMV-reverse transcriptase, MMLV-reverse transcriptase and HIV-reverse transcriptase, or exonuclease deficient variants of these polymerases.

15. The method of claim 1 or 5, wherein said reaction mixture in said initiating step further includes EDTA.

16. The method of claim 2 or 6, wherein said divalent cation is magnesium.

17. The method of claim 2 or 6, wherein said divalent cation is manganese.

18. The method of claim 1, further comprising:

prior to said detecting step d), adding a divalent cation to complete said polymerization reaction.

19. The method of sequencing a target region of a nucleic acid template of claim 18, further comprising:

f) removing said divalent cation and other end products from said polymerization reaction; and

g) repeating steps a) through f) for determining each additional nucleotide sequence.

5. A method for parallel characterization of a target region of a plurality of nucleic acid templates, comprising:

a) immobilizing a plurality of primers or nucleic acid templates on a support structure, wherein each primer or template contains a unique sequence and wherein multiple copies of each primer or template are localized to an identifiable, discrete location on said support structure;

b) initiating a plurality of nucleic acid polymerization reactions on said support structure, by forming a reaction mixture, said reaction mixture including said plurality of primers, said plurality of nucleic acid templates, a nucleic acid polymerizing enzyme, and at least one terminal-phosphate-labeled nucleotides each containing a distinct label, wherein each of said at least one terminal-phosphate-labeled nucleotides contains a base complementary to each of the four naturally occurring bases;

c) progressing said nucleic acid polymerization reactions by incubating said reaction mixture to form a plurality of complexes, each comprising one of said plurality of primers, one of said plurality of nucleic acid template, said nucleic acid polymerizing enzyme, and a terminal-phosphate-labeled nucleotide, wherein said terminal-phosphate-labeled nucleotide contains a base complementary to the template base at the site of polymerization;

d) removing unbound terminal-phosphate-labeled nucleotides and other components of said reaction mixture;

e) detecting, at each of said identifiable, discrete locations, the distinct label of said terminal-phosphate-labeled nucleotide from said complex;

f) recording data obtained from step e) to a data storage media; and

g) characterizing said target region sequence of each of said plurality of nucleic acid templates by converting said data to one of said four nucleotides.

6. The method for parallel characterization of a target region of a plurality of nucleic acid templates of claim 5, further comprising:

h) adding a divalent cation to complete said polymerization reactions;

i) removing said divalent cation and other end products from said polymerization reactions; and

j) repeating steps a) through i) for the characterization of each additional nucleotide of said plurality of nucleic acid templates.

7. The method of claim 5 wherein said support structure is beads, and wherein said beads carry one primer is identifiably separated from said beads carrying a different primer.

10-11. -11. (canceled)

20-21. -21. (canceled)

22. A method of analyzing a target region of a nucleic acid template, comprising:

a) initiating a nucleic acid polymerization reaction on a support, by forming a reaction mixture, said reaction mixture including a nucleic acid template, a primer, a nucleic acid polymerizing enzyme, and one to four nucleotides each containing a distinct label, wherein a component of said reaction mixture or a first complex of two or more of said components, is immobilized on said support, and said component or components are selected from the group consisting of said nucleic acid template, said primer, and said nucleic acid polymerizing enzyme, and wherein one of said one to four labeled nucleotides contains a base complementary to the template base at the site of polymerization;

b) incubating said reaction mixture to form a second complex comprising said nucleic acid template, said primer, said nucleic acid polymerizing enzyme, and one of said at least one labeled nucleotide, wherein said labeled nucleotide contains a base complementary to the template base at the site of polymerization, and wherein said labeled nucleotide is in dynamic equilibrium within said second complex;

c) detecting said label of said labeled nucleotide; and

d) identifying the sequence based on the detected distinctive label.

23. The method of analyzing a target region of a nucleic acid template of claim 22, further comprising:

e) removing, from said reaction mixture, said at least one labeled nucleotides and other unbounded components of said reaction mixture;

f) adding, to said reaction mixture, a nucleic acid polymerizing enzyme, a divalent cation, and a nucleotide containing the base complementary to the template base at the site of polymerization;

g) completing said polymerization reaction by incubating said reaction mixture for a period of time;

h) removing said divalent cation and other end products from said polymerization reaction; and

i) repeating steps a) through h) for each additional nucleotide to be sequenced.

27. The method of claim 22 further comprising:

prior to said detecting step c), removing, from said reaction mixture, said at least one labeled nucleotides and other unbound components of said reaction mixture.

24. A method for parallel analysis of a plurality of nucleic acid templates, comprising:

a) immobilizing a plurality of primers on a support structure, wherein each primer contains a unique sequence and wherein multiple copies of each primer are localized to an identifiable, discrete location on said support structure;

b) initiating a plurality of nucleic acid polymerization reactions on said support structure, by forming a reaction mixture, said reaction mixture including said plurality of immobilized primers, a plurality of nucleic acid templates, a nucleic acid polymerizing enzyme, and four labeled nucleotides each containing a distinct label, wherein each of said four labeled nucleotides contains a base complementary to each of the four naturally occurring bases;

c) incubating said reaction mixture to form a plurality of second complexes, each comprising one of said plurality of immobilized primers, one of said plurality of nucleic acid templates, said nucleic acid polymerizing enzyme, and a labeled nucleotide, wherein said labeled nucleotide contains a base complementary to the template base at the site of polymerization, and wherein said labeled nucleotide is in dynamic equilibrium within said second complex;

d) detecting, at each of said identifiable, discrete locations, said label of said labeled nucleotide;

e) recording data obtained from step d) to a data storage media; and

f) characterizing said target sequence of each of said plurality of nucleic acid templates by converting said recorded data to one of said four nucleotides.

29. The method of claim 24, further comprising:

prior to said detecting step d) removing, from said reaction mixture, said labeled nucleotides and other components of said reaction mixture.

25. A method for parallel analysis of a plurality of nucleic acid templates, comprising:

a) immobilizing a plurality of primers on a support structure, wherein each primer contains a unique sequence and wherein each primer is localized to an identifiable, discrete location on said support structure;

b) initiating a plurality of nucleic acid polymerization reactions on said support structure, by forming a reaction mixture, said reaction mixture including said plurality of immobilized primers, a plurality of nucleic acid templates, a nucleic acid polymerizing enzyme, and one labeled nucleotide;

c) incubating said reaction mixture to form a plurality of second complexes, each comprising one of said plurality of immobilized primers, one of said plurality of nucleic acid templates, said nucleic acid polymerizing enzyme, and said labeled nucleotide, wherein said labeled nucleotide contains a base complementary to the template base at the site of polymerization, and wherein said labeled nucleotide is in dynamic equilibrium within said second complex;

d) detecting, at said identifiable, discrete locations, said label of said labeled nucleotide;

e) recording data obtained from said detecting step to a data storage media;

f) removing, from said reaction mixture, said labeled nucleotides and other components of said reaction mixture;

g) adding, to said reaction mixture, a nucleic acid polymerizing enzyme, a divalent cation, and an un-labeled equivalent of said labeled nucleotide;

h) completing said polymerization reaction by incubating said reaction mixture for a period of time;

i) removing said divalent cation and other end products from said polymerization reaction;

j) repeating steps a) through i) with one of the other three nucleotides, until all four nucleotides are tested; and

k) repeating steps a) through j) for determining additional nucleotide sequences.

26. The method of claim 25, further comprising the step of:

l) characterizing said target sequences of said plurality of nucleic acid templates by converting said recorded data to sequence of one of said four nucleotides and assembling said target sequence for each of said plurality of nucleic acid templates.

32. The method of claim 25, wherein the order of addition of labeled nucleotides occurs in a preset cycle.

33. The method of claim 25, wherein said first removing step f) is performed prior to said detecting step d).

28. (canceled)

30-31. -31. (canceled)