Method for analyzing luminescent species

Patent metadata

Field	Value
Publication number	US-10901145-B2
Application number	US-201816201670-A
Country	US
Kind code	B2
Filing date	Nov 27, 2018
Priority date	Sep 11, 2009
Publication date	Jan 26, 2021
Grant date	Jan 26, 2021

Abstract

The application relates to methods of analyzing luminescent species. A substrate is provided that has a plurality of zero mode waveguides having apertures that extend through an upper non-reflective layer that is disposed on a lower transparent layer of a substrate. The apertures have non-reflective oxide layers on the reflective side walls of the apertures, the side walls having a thickness of greater than 10 nm, and the oxide layer is formed by oxidizing the non-reflective layer. The volume within the oxide layer defines a solution volume, and the volume within the reflective walls defines a ZMW volume. Having such non-reflective layers on the walls of the ZMW usefully decouples the solution volume from the ZMW volume.

First claim

What is claimed is:

1. A method for analyzing a luminescent species comprising:
a) providing a substrate comprising a plurality of zero mode waveguides comprising a plurality of apertures that extend through an upper non-reflective layer that is disposed on a lower transparent layer of the substrate, wherein the apertures comprise reflective side walls, and wherein each of the apertures comprises a non-reflective oxide layer on the reflective side walls having a thickness of greater than 10 nm, wherein the oxide layer is formed by oxidizing the upper non-reflective layer, whereby there is a volume within the oxide layer of each zero mode waveguide that defines a solution volume, and whereby there is a volume within the reflective walls of each zero mode waveguide that defines a ZMW volume;
b) providing a solution comprising luminescent species in contact with the substrate whereby the luminescent species are present in the solution volume of the plurality of apertures, and
c) detecting emitted light from the luminescent species in the solution volume of the plurality of apertures wherein the emitted light from the luminescent species passes through the lower transparent layer.

2. The method of claim 1 wherein the solution volume of each of the zero-mode waveguides is less than about 80% of the ZMW volume of that zero-mode waveguide.

3. The method of claim 1 wherein the solution volume of each of the zero-mode waveguides is less than about 70% of the ZMW volume of that zero-mode waveguide.

4. The method of claim 1 wherein the luminescent species comprise fluorescent species, the method further comprising illuminating the fluorescent species with illumination light.

5. The method of claim 1 wherein the luminescent species is associated with a biomolecule.

6. The method of claim 1 wherein the luminescent species is covalently attached to an enzyme substrate and wherein the emitted light provides information regarding an interaction of the enzyme substrate with the enzyme.

7. The method of claim 1 wherein each of the plurality of apertures comprise a complex of a polymerase enzyme, a nucleic acid template, and a primer, such complex capable of adding a complementary nucleotide, and wherein the emitted light provides information about the addition of the nucleotide.

8. The method of claim 7 wherein the luminescent species is covalently attached to the enzyme, the nucleotide, the template, or the primer.

9. The method of claim 7 wherein the luminescent species is covalently attached to the nucleotide.

10. The method of claim 9 wherein the polymerase enzyme is selectively bound to the lower transparent layer of the substrate.

11. The method of claim 1 wherein the upper non-reflective layer comprises a metal.

12. The method of claim 11 wherein the metal comprises aluminum, silver, or titanium.

13. The method of claim 1 wherein the upper non-reflective layer comprises aluminum.

14. The method of claim 1 wherein the plurality of apertures comprise cylinders.

15. The method of claim 1 wherein the plurality of apertures have a cylindrical profile and the apertures have a zero mode waveguide diameter within the reflective walls of 70 nm to 300 nm.

16. The method of claim 1 wherein the plurality of apertures comprise conical structures.

17. The method of claim 1 wherein the non-reflective oxide layer is formed by chemical oxidation.

18. The method of claim 1 wherein the non-reflective oxide layer is formed electrochemically.

19. The method of claim 1 wherein the non-reflective oxide layer is formed with an oxygen plasma.

Assignees

• Pacific Biosciences California Inc

Inventors

• Gray Jeremy
• Sun Lei

Classifications

• C25D11/022 Primary

  Anodisation on selected surface areas · CPC title

• C23F1/00

  Etching metallic material by chemical means (manufacture of printing surfaces B41C; manufacture of printed circuits H05K) · CPC title

• G02B6/107 Primary

  Subwavelength-diameter waveguides, e.g. nanowires · CPC title

• G02B6/10

  of the optical waveguide type (G02B6/02, G02B6/24 take precedence; devices or arrangements for the control of light by electric, magnetic, electro-magnetic or acoustic means G02F1/00; transferring the modulation of modulated light G02F2/00; optical logic elements G02F3/00; optical analogue/digital converters G02F7/00) · CPC title

• G02B6/136

  by etching · CPC title