MATERIALS AND METHODS FOR SINGLE MOLECULE NUCLEIC ACID SEQUENCING

• US 20100035268A1
• Filed: 02/21/2008
• Published: 02/11/2010
• Est. Priority Date: 02/21/2007
• Status: Abandoned Application

• Current Assignee: Life Technologies Corporation (Thermo Fisher Scientific Incorporated)
• Original Assignee: Life Technologies Corporation (Thermo Fisher Scientific Incorporated)
• Inventors: Beechem, Joseph, Nikiforov, Theo, Choong, Vi-En
• Application Number:
  US12/528,311
• Publication Number:
  US 20100035268A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C12Q 2563/113 the label being electroactive, e.g. redox labels
• CPC Class Codes: C12Q 2565/101 Interaction between at least two labels
• CPC Class Codes: C12Q 2565/518 characterised by the immobilisation of the nucleic acid sample or target

Abstract

Provided herein are methods and compositions for real time single molecule sequencing of short nucleotide sequences using nucleotide fluorescent semiconductor nanocrystals-conjugated nucleotide primers.

Claims

1. A method for genotyping or sequencing a single target nucleic acid molecule, said method comprising:

a) immobilizing onto a solid support a target nucleic acid molecule to form a solid support comprising more than one site or location each bearing only one individual molecule of target nucleic acid sequence;

b) contacting the solid support with a polymerase, a primer operably linked to at least one semiconductor nanocrystal, and at least one fluorescent labeled nucleotide polyphosphate;

c) optically detecting a time sequence of incorporation of the fluorescently labeled nucleotide polyphosphates into the growing nucleotide strand at an active site complementary to the target nucleic acid molecule, by detecting fluorescence resonance energy transfer (FRET) signals between the semiconductor nanocrystal and the fluorescent labeled nucleotide polyphosphate,

wherein the identity of each fluorescent labeled nucleotide is determined by its fluorescent label,

wherein the fluorescent label is then cleaved from the nucleotide upon incorporation into the growing strand; and

d) genotyping or sequencing said single target nucleic acid molecule by converting the sequence of the FRET signals detected during the polymerization reaction into a nucleic acid sequence.

2. The method of claim 1, wherein the target nucleic acid molecule is DNA, and the polymerase is a DNA or RNA polymerase.

3. The method of claim 1, wherein the target nucleic acid molecule is RNA, and the polymerase is reverse transcriptase.

4. The method of claim 1, wherein the polymerase is a Klenow fragment of DNA polymerase I, E. coli DNA polymerase I, T7 DNA polymerase, T4 DNA polymerase, Thermus aquaticus DNA polymerase, or Thermococcus litoralis, DNA polymerase.

5. The method of claim 1, wherein the semiconductor nanocrystal acts as a donor fluorophore and the fluorescent label on the nucleotide polyphosphate acts as the acceptor fluorophore.

6. The method of claim 1, wherein the fluorescent label is selected from the group consisting of fluorescein, cyanine, rhodamine, coumarin, acridine, Texas Red dye, BODIPY, ALEXA, and a derivative or modification of any of the foregoing.

7. The method of claim 1, wherein the fluorescent label is attached to the γ

-phosphate of the nucleotide polyphosphate.

8. The method of claim 1, wherein the detection occurs in real-time or near real-time.

9. The method of claim 1, further comprising sequencing a second nucleic acid according to the method of claim 1 in parallel with sequencing the first nucleic acid.

10. The method of claim 1, wherein the solid support is glass or plastic.

11. The method of claim 4, wherein the primer is extended by a plurality of nucleotides.

12. The method of claim 5, wherein the primer is extended by less than 50 nucleotides.

13. The method of claim 1, wherein the primer comprises at least 10 nucleotides.

14. The method of claim 1, wherein the primer comprises at least 20 nucleotides.

15. The method of claim 1, wherein the fluorescent labeled nucleotide polyphosphate has three or more phosphates.

16. The method of claim 1, wherein the fluorescent labeled nucleotide polyphosphate has four or more phosphates.