Apparatus and method for performing nucleic acid analysis
The present invention relates to optical confinements, methods of preparing and methods of using them for analyzing molecules and/or monitoring chemical reactions. The apparatus and methods embodied in the present invention are particularly useful for high-throughput and low-cost single-molecular analysis.
1. A nucleic acid sequencing method comprising:
subjecting a target nucleic acid molecule to a template-directed polymerization reaction to yield a nascent nucleic acid strand that is complementary to the target nucleic acid molecule in the presence of a plurality of types of nucleotides or nucleotide analogs, and a polymerization enzyme exhibiting strand-displacement activity, wherein said template-directed polymerization reaction processes an identical sequence of nucleotides in the target nucleic acid molecule more than once; registering a time sequence of incorporation of nucleotides or nucleotide analogs into the nascent nucleotide strand; and determining a sequence of nucleotides in the target sequence.
2. The method of claim 1 , wherein the target nucleic acid molecule is a circular nucleic acid.
3. The method of claim 2 , wherein the target nucleic acid molecule is a circular DNA.
4. The method of claim 2 , wherein said template-directed polymerization reaction processes a sequence of nucleotides in the circular nucleic acid multiple times.
5. The method of claim 1 , wherein the target nucleic acid molecule comprises a sequence of nucleotides that is present multiple times within the target nucleic acid molecule.
6. The method of claim 1 , wherein the target nucleic acid comprises a product of a template dependent replication of a circular nucleic acid.
7. Previously Presented) The method of claim 1 , wherein the polymerization enzyme is a modified or unmodified φ29 DNA polymerase.
8. The method of claim 1 , wherein said target nucleic acid molecule is sequenced more than once by the polymerization enzyme.
9. The method of claim 1 , wherein aid target nucleic acid molecule is sequenced more than twice by the polymerization enzyme.
10. The method of claim 1 , wherein the nucleotides or nucleotide analogs further comprise a label.
11. The method of claim 10 , wherein the label is attached to the nucleotides or nucleotide analogs at a base, sugar moiety, alpha phosphate, or beta phosphate, of said nucleotides or nucleotide analogs.
12. The method of claim 10 , wherein the label is attached to the nucleotides or nucleotide analogs at a terminal phosphate.
13. The method of claim 10 , wherein the label is on a terminal phosphate of a nucleotide or nucleotide analog, comprising a phosphate moiety selected from the group consisting of monophosphate, diphosphate, triphosphate, tetraphosphate, pentaphosphate, and hexaphosphate.
14. The method of claim 10 , wherein each type of the nucleotides or nucleotide analogs has a different label which is distinguished from one another during said registering step.
15. The method of claim 10 , wherein the label is a fluorescence resonance energy transfer donor or acceptor.
16. The method of claim 1 , wherein said target nucleic acid molecule is attached to a support.
17. The method of claim 1 , wherein said target nucleic acid molecule is hybridized to primer which is attached to a support.
18. The method of claim 1 , wherein said polymerization enzyme is attached to a support.
19. The method of claim 1 , wherein said registering is performed while the template-directed polymerization reaction is taking place.
20. The method of claim 1 , wherein said registering step comprising identifying nucleotides or nucleotide analogs provided in said plurality of types of nucleotides or nucleotide analogs.
21. The method of claim 1 , wherein the template-directed polymerization reaction takes place in an optical confinement.
22. The method of claim 1 , wherein the template-directed polymerization reaction takes place in an array of optical confinements.
23. The method of claim 1 , wherein the template-directed polymerization reaction takes place in a zero-mode waveguide.
24. The method of claim 1 , wherein the target nucleic acid molecule and the polymerization enzyme form a single complex immobilized in an optical confinement.
25. The method of claim 24 , wherein the array of optical confinements has a fill fraction greater than 0.0001.
26. The method of claim 24 , wherein the array of optical confinements has a fill fraction greater than 0.01.
27. The method of claim 24 , wherein the array of optical confinements has a fill fraction between 0.00 and 0.1
28. The method of claim 24 , wherein the array of optical confinements has a fill fraction greater than 0.1.
29. The method of claim 22 , wherein the array of optical confinements has a density on a substrate exceeding 4 ×10 4 confinements per mm 2 .
30. The method of claim 22 , wherein the array of optical confinements has a density on a substrate exceeding 10 5 confinements per mm 2 .