Method for binding reactive groups in observation area of zero mode waveguide

• US 7,993,891 B2
• Filed: 10/31/2007
• Issued: 08/09/2011
• Est. Priority Date: 09/30/2005
• Status: Active Grant

• Current Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Original Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Inventors: Peluso, Paul, Roitman, Daniel, Foquet, Mathieu
• Primary Examiner(s): Naff; David
• Application Number:
  US11/981,551
• Publication Number:
  US 20090061429A1
• Time in Patent Office: 1,378 Days
• Field of Search: None
• US Class Current: 435/174
• CPC Class Codes: B01J 2219/00605 the compounds being directly bound or immobilised to solid supports
• CPC Class Codes: B01J 2219/0061 The surface being organic
• CPC Class Codes: B01J 2219/00612 the surface being inorganic
• CPC Class Codes: B01J 2219/00626 Covalent
• CPC Class Codes: B01J 2219/00628 Ionic
• CPC Class Codes: B01J 2219/0063 Other, e.g. van der Waals forces, hydrogen bonding
• CPC Class Codes: B01J 2219/00637 by coating it with another layer
• CPC Class Codes: B01J 2219/00659 Two-dimensional arrays
• CPC Class Codes: B01J 2219/00722 Nucleotides
• CPC Class Codes: B01J 2219/00725 Peptides
• CPC Class Codes: G01N 33/543 with an insoluble carrier for immobilising immunochemicals
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing
• CPC Class Codes: G01N 33/54393 Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding

Abstract

Reactive surfaces, substrates and methods of producing and using such substrates and surfaces are provided. The substrates and surfaces provide low density reactive groups preferably on an otherwise non-reactive surface for use in different applications including single molecule analyses.

Claims

1. A method for binding reactive groups in an observation area of a zero mode waveguide comprising;

providing a zero mode waveguide comprising a cladding layer on a transparent base substrate, and an aperture having wall surfaces extending through the cladding layer to the transparent base substrate where the wall surfaces of the aperture contact the transparent base substrate to provide an observation area having a cross-sectional dimension of the aperture on the transparent base substrate;

coupling a layer of exclusion molecules to the wall surfaces of the aperture, such that the observation area for binding of reactive groups is reduced; and

binding reactive groups to the observation area whereby the exclusion molecules coupled to the wall surfaces of the aperture sterically exclude binding of the reactive groups to the observation area to reduce the radius of the observation area for binding the reactive groups.

2. The method of claim 1 wherein the reactive groups comprise catalytic reactive, groups.

3. The method, of claim 1 wherein the reactive groups comprise enzymes.

4. The method of claim 1 wherein the exclusion molecules provide only sufficient space for the coupling of a single reactive group.

5. The method of claim 1 wherein the exclusion molecules provide only sufficient space for the coupling of a single catalytic reactive group.

6. The method of claim 1 wherein the exclusion molecules provide only sufficient space for the coupling of a single enzyme.

7. The method of claim 1 wherein the zero mode waveguide is in an array of zero mode waveguides.

8. The method of claim 1 wherein the exclusion molecules comprise polymers.

9. The method of claim 1 wherein the exclusion molecules comprise proteins.

10. The method of claim 1 wherein the cladding comprises a metal, and wherein the exclusion molecules comprise metal chelating groups.

11. The method of claim 1 wherein the aperture has a cross-sectional, dimension from about 20 nm to about 200 nm.

12. The method of claim 1 wherein the reactive groups are bound near the center of the observation area.

13. An array of zero mode waveguides, each zero mode waveguide comprising:

a cladding layer on a transparent base substrate, an aperture having wall surfaces extending through the cladding layer to the transparent base substrate where the wall surfaces of the aperture contact the transparent base substrate to provide an observation area having cross-sectional dimension of the aperture on the transparent base substrate for binding reactive groups, and a layer of exclusion molecules coupled to wall surfaces of the aperture, such that the exclusion molecules sterically exclude binding of the reactive groups to the observation area to reduce the radius of the observation area for binding the reactive groups.

14. The array of claim 13 wherein the exclusion molecules comprise polymers.

15. The array of claim 13 wherein the exclusion molecules comprise proteins.

16. The array of claim 13 wherein the cladding comprises a metal, and wherein the exclusion molecules comprise metal chelating groups.

17. The array of claim 13 wherein the aperture has a cross-sectional dimension from about 20 nm to about 200 nm.

18. The array of claim 13 further comprising one or more reactive groups.

19. The array of claim 18 wherein the reactive groups comprise catalytic reactive groups.

20. The array of claim 18 wherein the reactive groups comprise enzymes.

21. The array of claim 18 wherein the reactive groups comprise biotin.

22. The array of claim 18 wherein at least some of the zero mode waveguides comprise a single reactive group.

23. The array of claim 22 wherein the single reactive group comprises a single catalytic reactive group.

24. The array of claim 22 wherein the single reactive group comprises an enzyme.

25. The array of claim 18 wherein the reactive groups are near the center of the observation area.