Loading molecules onto substrates
Disclosed are compositions, devices, and methods for loading molecules of interest onto a substrate by contacting beads having molecules of interest attached to them with the substrate, for example by providing a field that brings the beads into proximity or contact with the substrate and moves the beads with respect to the substrate. Such molecules of interest can be deposited onto substrates for single-molecule analysis.
1. A method for loading polymerase-nucleic acid complexes onto a substrate comprising:
providing a solution of beads, individual beads having bound thereto a plurality of polymerase-nucleic acid complexes,
exposing the solution to a substrate, wherein the substrate comprises an array of zero mode waveguides, and wherein the beads have diameters that are greater than the smallest cross-sectional dimension of the zero mode waveguides, the substrate comprising coupling groups for coupling the polymerase-nucleic acid complexes to the substrate within the zero mode waveguides; and
applying a field to draw the particles to the substrate, whereby polymerase-nucleic acid complexes become bound to the substrate through the coupling groups.
2. The method of claim 1 further comprising applying a field that moves the particles across the surface of the substrate.
3. The method of claim 1 further comprising removing the beads from the substrate, leaving the bound polymerase-nucleic acid complexes on the substrate.
4. The method of claim 1 wherein the field is a magnetic, electric, or gravitational field.
5. The method of claim 2 wherein the field to draw the particles to the substrate and the field to move the polymerase-nucleic acid complexes comprise different types of fields.
6. The method of claim 2 wherein the field to draw the particles to the substrate and the field to move the polymerase-nucleic acid complexes comprise the same type of field.
7. The method of claim 6 wherein the field comprises a magnetic field.
8. The method of claim 7 wherein the magnetic field is applied using one or more permanent magnets that are moved relative to the substrate.
9. The method of claim 7 wherein the magnetic field is applied using one or more electromagnets.
10. The method of claim 1 wherein a portion of the zero mode waveguides have a single polymerase-nucleic acid complex attached thereto.
11. The method of claim 1 wherein the diameter of the bead is 2 times greater or more than the smallest cross-sectional dimension of the zero mode waveguide.
12. The method of claim 1 wherein the diameter of the bead is 2 times greater to 10,000 times greater than the smallest cross-sectional dimension of the zero mode waveguide.
13. The method of claim 1 wherein the zero mode waveguides are cylindrical, and the smallest cross sectional dimensions are the diameters of the zero mode waveguides.
14. A method for loading active polymerase-nucleic acid complexes onto a substrate comprising:
providing a solution of magnetic beads having poiymerase-nucleic acid complexes bound thereto, each polymerase-nucleic acid complex comprising a polymerase enzyme, and a template nucleotide;
contacting the solution of magnetic beads with the top of a substrate comprising an array of nanoscale wells having bases, wherein the bases of the wells have coupling agent bound thereto, wherein the beads have diameters that are greater than the smallest cross-sectional dimension of the nanoscale wells; and
applying a dynamic magnetic field to move the magnetic beads in solution down to the top of the substrate, whereby the dynamic magnetic field also causes the particles to be moved across the top surface of the substrate, whereby some polymerase-nucleic acid complexes become bound to the coupling groups on the bases of the nanoscale wells.
15. The method of claim 14 wherein the polymerase-nueleic acid complexes are bound to the magnetic beads via hybridization between an oligonucleotide attached to the magnetic bead and a sequence on the template nucleic acid.
16. The method of claim 14 wherein the magnetic bead is attached to a hook oligonucleotide comprising a retrieval sequence that is complimentary to an oligonucleotide attached to the magnetic bead and a capture sequence that is complementary to the template nucleic acid.
17. The method claim 14 wherein the nanoscale wells are cylindrical, and the smallest cross sectional dimensions are the diameters of the nanoscale wells.
18. A method of loading a polymerase-nucleic acid complex onto a substrate, wherein the substrate comprises an array of zero mode waveguides comprising:
providing a double-stranded DNA sample;
treating the double-stranded DNA sample with terminal transferase in the presence of dATP to add poly(A) regions to the 3′ ends of the DNA sample;
adding a hook oligonucleotide comprising a 3′ poly(T) region and a 5′ retrieval region under conditions where hybridization of the poly(T) region of the hook oligonucleotide to the poly(A) region of the DNA sample occurs;
adding a polymerase enzyme under conditions where the enzyme will form a polymerase-nucleic acid complex;
adding beads comprising sequences that are complementary to the retrieval sequence on the hook oligonucleotide under conditions where hybridization occurs;
exposing the beads comprising the polymerase-nucleic acid complexes to a substrate, wherein the beads have diameters that are greater than the smallest cross-sectional dimension of the zero mode waveguides; and
applying a field to bring the beads down to the surface to load the polymerase-nucleic acid complexes onto the surface.
19. The method of claim 18 further comprising applying a field that moves the particles across the surface of the substrate.
20. The method of claim 18 further comprising removing the beads from the substrate, leaving the bound polymerase-nucleic acid complexes on the substrate.
21. The method of claim 18 wherein the field comprises a magnetic field.
22. The method of claim 21 wherein the magnetic field is applied using one or more permanent magnets that are moved relative to the substrate.