Substrates and methods for selective immobilization of active molecules

• US 20080220537A1
• Filed: 03/05/2008
• Published: 09/11/2008
• Est. Priority Date: 03/07/2007
• Status: Abandoned Application

• Current Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Original Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Inventors: Foquet, Mathieu
• Application Number:
  US12/074,716
• Publication Number:
  US 20080220537A1
• Time in Patent Office: Days
• US Class Current: 436/518
• CPC Class Codes: B01J 2219/00605 the compounds being directly bound or immobilised to solid supports
• CPC Class Codes: B01J 2219/00617 by chemical means
• CPC Class Codes: B01J 2219/00621 by physical means, e.g. trenches, raised areas
• CPC Class Codes: B01J 2219/00637 by coating it with another layer
• CPC Class Codes: B01L 2200/12 Specific details about manufacturing devices
• CPC Class Codes: B01L 2300/0636 Integrated biosensor, microarrays
• CPC Class Codes: B01L 2300/0654 Lenses; Optical fibres
• CPC Class Codes: B01L 2300/0819 Microarrays; Biochips
• CPC Class Codes: B01L 3/5085 for multiple samples, e.g. microtitration plates
• CPC Class Codes: G01N 2021/0346 Capillary cells; Microcells

Abstract

Substrates and methods for providing increased selectivity in the immobilization of active molecules of interest in desired locations of substrates for use in analytical operations and particularly optical analytical operations.

Claims

1. A substrate having active molecules of interest disposed thereon, comprising:

a first layer having a first surface;

a second layer disposed over a portion of the first surface;

wherein the second layer comprises a material having a substantially increased or decreased ability to bind the active molecules of interest, relative to the first layer;

active molecules of interest preferentially bound to one of the first and second layers.

2. The substrate of claim 1, wherein the second layer has a substantially increased ability to bind the molecules of interest relative to the first layer.

3. The substrate of claim 1, wherein the second layer has a substantially increased ability to bind the molecules of interest relative to the first layer.

4. The substrate of claim 2, wherein the molecules of interest are bound to the second layer relative to the first layer at a ratio of at least 5:

1.

5. The substrate of claim 2, wherein the molecules of interest are bound to the second layer relative to the first layer at a ratio of at least 10:

1.

6. The substrate of claim 2, wherein the molecules of interest are bound to the second layer relative to the first layer at a ratio of at least 50:

1.

7. The substrate of claim 2, wherein the molecules of interest are bound to the second layer relative to the first layer at a ratio of at least 100:

1.

8. The substrate of claim 1, wherein the second layer has a substantially decreased ability to bind the molecules of interest relative to the first layer.

9. The substrate of claim 2, wherein the molecules of interest are bound to the first layer relative to the second layer at a ratio of at least 5:

1.

10. The substrate of claim 2, wherein the molecules of interest are bound to the first layer relative to the second layer at a ratio of at least 10:

1.

11. The substrate of claim 2, wherein the molecules of interest are bound to the first layer relative to the second layer at a ratio of at least 50:

1.

12. The substrate of claim 2, wherein the molecules of interest are bound to the first layer relative to the second layer at a ratio of at least 100:

1.

13. The substrate of claim 1, further comprising a third layer disposed over at least a portion of the second layer.

14. The substrate of claim 1, further comprising a third layer disposed between the portion of the first surface of the first layer and the second layer.

15. The substrate of claim 1, wherein the first layer comprises a transparent layer and the second layer comprises a metal layer.

16. The substrate of claim 15, wherein the metal layer comprises a metal layer having a substantially increased ability to bind the molecules of interest relative to the transparent layer.

17. The substrate of claim 16, wherein the metal layer comprises gold, and the molecules of interest are bound to the second layer through thiol groups.

18. The substrate of claim 1, wherein the second layer comprises an opaque material disposed upon the first surface and further comprising a plurality of apertures disposed through the second layer to the first surface.

19. The substrate of claim 1, wherein the third layer is disposed over the second layer and further comprising a plurality of apertures disposed through the second and third layers to the first surface thereby exposing a portion of the second layer.

20. The substrate of claim 14, wherein the second layer comprises a material having a decreased ability to bind active molecules of interest.

21. The substrate of claim 20, wherein the material of the second layer has a deactivating influence on an activity of the molecules of interest.

22. The substrate of claim 21, wherein the material of the second layer comprises an enzyme having a deactivating influence on the activity of the active molecules of interest.

23. The substrate of claim 21, wherein the material of the second layer comprises TiO₂.

24. The substrate of claim 1, wherein the active molecules of interest comprise nucleic acid polymerase enzymes.

25. A method of selectively providing active molecules of interest in a first location on a substrate, comprising:

providing a first substrate layer having a first surface;

providing a second layer disposed over a portion of the first surface, the second layer having an increased ability to bind the active molecules of interest relative to the first layer;

providing a third layer disposed over at least a portion of the second layer, the third layer having a substantially descreased ability to bind the molecules of interest relative to the second layer, and a portion of the second layer remaining exposed; and

contacting the substrate with the molecules of interest to coupled active molecules of interest preferentially to the portion of the second layer that is exposed, relative to an exposed portion of the first layer and the third layer.

26. A method of analyzing an active molecule of interest, comprising:

providing a layered substrate comprising;

a first transparent layer;

a second layer disposed over the first transparent layer, the second layer having a substantially increased ability to bind the active molecules of interest relative to the first transparent layer;

a third layer disposed over the second layer;

a plurality of apertures disposed through the second and third layers to provide an observation aperture through the transparent layer, an internal wall of the apertures exposing a portion of the second layer; and

active molecules of interest preferentially bound to the portion of the second layer exposed in the apertures;

observing activity of the active molecules of interest through the observation aperture in the transparent substrate.