Nanogrid rolling circle DNA sequencing
The present invention relates to methods for sequencing a polynucleotide immobilized on an array having a plurality of specific regions each having a defined diameter size, including synthesizing a concatemer of a polynucleotide by rolling circle amplification, wherein the concatemer has a cross-sectional diameter greater than the diameter of a specific region, immobilizing the concatemer to the specific region to make an immobilized concatemer, and sequencing the immobilized concatemer.
1. A method of sequencing a polynucleotide immobilized on an array comprising:
synthesizing a concatemer of a polynucleotide by rolling circle amplification;
immobilizing the concatemer to the array, wherein the array comprises a substrate having a plurality of specific functionalized regions attached to the substrate in a pattern forming an ordered array, wherein each specific functionalized region comprises an inner spot functionalized with a first group which serves to capture the concatemer and an outer spot functionalized with a second group which serves as an attachment point for an amplification primer, wherein the concatermer is immobilized to the inner spot, and wherein the concatemer has a cross-sectional diameter greater than the diameter of the inner spot; and
sequencing the immobilized concatemer.
2. The method of claim 1 , wherein the concatemer has a cross-sectional diameter of at least 200 nanometers.
3. The method of claim 1 , wherein the concatemer has a cross-sectional diameter of at least 300 nanometers.
4. The method of claim 1 , wherein the polynucleotide is DNA.
5. The method of claim 1 , wherein one concatemer is immobilized at the plurality of specific functionalized regions.
6. The method of claim 1 , wherein the array has at least 100 specific functionalized regions.
7. The method of claim 6 , wherein one concatemer is immobilized at each of the plurality of specific functionalized regions.
8. The method of claim 6 , wherein at least 90 of the specific functionalized regions each contains one immobilized concatemer.
9. The method of claim 1 , wherein the array has at least 1000 specific functionalized regions.
10. The method of claim 1 , wherein the array has at least 10,000 specific functionalized regions.
11. The method of claim 1 , wherein sequencing the immobilized concatemer is performed by fluorescent in situ sequencing.
12. The method of claim 1 , wherein the array is a nanoarray.
13. The method of claim 1 , wherein optical magnification is used to sequence the immobilized concatemer.
14. The method of claim 1 , wherein immobilization is performed by hybridization.
15. The method of claim 1 , wherein immobilization is performed by an interaction selected from the group consisting of biotin-avidin capture, biotin-streptavidin capture, NHS-ester capture, thioether linkage, static charge interactions and van der Waals forces.
16. A method of sequencing a polynucleotide immobilized on an comprising:
synthesizing a concatemer of a polynucleotide by rolling circle amplification
immobilizing the concatemer to the array, wherein the array comprises a substrate having a plurality of specific functionalized regions attached to the substrate in a pattern forming an ordered array, wherein each specific functionalized region comprises an inner spot functionalized with a first group which serves to capture the concatemer and an outer spot functionalized with a second group which serves as an attachment point for an amplification primer, wherein the concatermer is immobilized to the inner spot, and wherein the concatemer has a cross-sectional diameter greater than the diameter of the inner spot;
clonally amplifying the immobilized concatemer to make a clonally amplified concatemer; and
sequencing the clonally amplified concatemer.
17. The method of claim 16 , wherein clonally amplifying is performed by a method selected from the group consisting of rolling circle amplification, multiple displacement amplification, thermophilic helicase-dependent amplification and bridge PCR.
18. The method of claim 17 , wherein rolling circle amplification is selected from the group consisting of hyperbranched rolling circle amplification, padlock probe rolling circle amplification and linear rolling circle amplification.
19. The method of claim 1 , wherein immobilization is performed by biotin-avidin capture or NHS-ester capture.