Method for detecting biomolecules

• US 7,410,762 B1
• Filed: 06/27/2005
• Issued: 08/12/2008
• Est. Priority Date: 06/27/2005
• Status: Active Grant

• Current Assignee: National Technology & Engineering Solutions Of Sandia LLC (Honeywell International Inc.)
• Original Assignee: Sandia Corporation (Martin Marietta Corporation)
• Inventors: Liu, Jun, Huo, Qisheng
• Primary Examiner(s): WHISENANT, ETHAN C
• Application Number:
  US11/168,247
• Time in Patent Office: 1,142 Days
• Field of Search: 435/6, 435/7.1, 536/23.1, 536/24.3
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6825 Nucleic acid detection involving sensors

Abstract

A method for detecting and measuring the concentration of biomolecules in solution, utilizing a conducting electrode in contact with a solution containing target biomolecules, with a film with controllable pore size distribution characteristics applied to at least one surface of the conducting electrode. The film is functionalized with probe molecules that chemically interact with the target biomolecules at the film surface, blocking indicator molecules present in solution from diffusing from the solution to the electrode, thereby changing the electrochemical response of the electrode.

Claims

1. A method for detecting biomolecules, comprising:

contacting a solution containing target biomolecules and indicator molecules with a sensor platform, said sensor platform comprising a nanoporous film deposited on a conducting electrode, said nanoporous film functionalized with probe molecules that chemically interact with said target biomolecules, wherein said nanoporous film is a self-assembled film, said self-assembled film comprising a precursor sol, said precursor sol comprising an aqueous solution prepared from a surfactant, a solvent, and a compound selected from tetra-alkoxysilanes, an alkoxysilane, and a metal alkoxide, and measuring current across said conducting electrode to detect the presence of said target biomolecules.

2. The method of claim 1 where wherein said self-assembled film has a controllable pore size distribution with pores having diameters in the range of 1.5 nm to 30 nm.

3. The method of claim 2 wherein said pore size distribution has a value of the mean pore diameter divided by the variance of less than 4.

4. The method of claim 1 wherein said film is defect-free.

5. The method of claim 1 wherein the conducting electrode comprises a conducting substrate material.

6. The method of claim 1 wherein the conducting electrode comprises an indium tin oxide material.

7. The method of claim 1 wherein the conducting electrode comprises a non-conducting substrate material coated with a conducting film.

8. The method of claim 7 wherein the non-conducting substrate material is selected from a plastic, a glass, and a ceramic.

9. The method of claim 1 wherein said indicator compound is selected from iron phenanthroline, cobalt phenanthroline and ruthenium phenanthroline.

10. The method of claim 1 wherein said plurality of target biomolecules comprises a material selected from a protein and DNA.

11. The method of claim 1 wherein said surfactant is selected from an anionic surfactant, a cationic surfactant, a nonionic surfactant, and a block copolymer surfactant.

12. The method of claim 1 wherein said surfactant is a poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) triblock copolymer of the general formula EO_xPO_yEO_z.

13. The method of claim 12 wherein said surfactant is EO₁₀₆PO₇₀EO₁₀₆.

14. The method of claim 1 wherein said film is a self-assembled film, said self-assembled film comprising a precursor sol, said precursor sol comprising an aqueous solution prepared from EO₁₀₆PO₇₀EO₁₀₆, tetraethoxysilicate, and 3-aminopropyltriethoxysilicate under acidic conditions.

15. The method of claim 1 wherein said probe molecules comprise biotin and the target biomolecules comprise streptavidin.

16. The method of claim 1 wherein said target biomolecules comprise DNA molecules.

17. The method of claim 1 wherein said plurality of target biomolecules comprise a concentration of less than 10 nmoles in solution.

18. A method for detecting biomolecules, comprising:

contacting a solution containing target biomolecules with a sensor platform, said sensor platform comprising a nanoporous film deposited on a conducting electrode, said nanoporous film functionalized with probe molecules that chemically interact with said target biomolecules, and

measuring the potential difference between said solution and said conducting electrode to detect said target biomolecules.