Quality control of probe attachment on electrodes

• US 20070099194A1
• Filed: 11/02/2005
• Published: 05/03/2007
• Est. Priority Date: 11/02/2005
• Status: Abandoned Application

• Current Assignee: Geneohm Sciences Incorporated (Becton, Dickinson & Co)
• Original Assignee: Geneohm Sciences Incorporated (Becton, Dickinson & Co)
• Inventors: Yang, Xing, Zhu, Qun
• Application Number:
  US11/264,996
• Publication Number:
  US 20070099194A1
• Time in Patent Office: Days
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 2563/113 the label being electroactive, e.g. redox labels

Abstract

The present disclosure relates to methods of quantifying nucleic acid molecules immobilized on an electrode of an electrochemical assay chip. Such quantification can be used in testing and quality control of assay chips. Materials and instrumentation useful in performing such techniques are also disclosed.

Claims

1. A method of quantifying nucleic acid probes comprising:

providing an electrode surface;

immobilizing a plurality of nucleic acid probes on said electrode surface;

providing a redox moiety capable of electrostatic association with said plurality of nucleic acid probes; and

detecting a total electrical current transferred by said redox moiety, wherein said total electrical current comprises a diffusion current and an adsorption current, wherein said detection occurs at a frequency at which said adsorption current is greater than said diffusion current.

2. The method of claim 1 wherein said electrode surface comprises gold.

3. The method of claim 1 wherein said electrode surface comprises carbon.

4. The method of claim 1 wherein said redox moiety comprises ruthenium.

5. The method of claim 4 wherein said redox moiety is ruthenium hexamine.

6. The method of claim 1 wherein said frequency is greater than about 50 Hz.

7. The method of claim 1 wherein said frequency is greater than about 200 Hz.

8. The method of claim 1 wherein said frequency is about 300 Hz.

9. The method of claim 1 wherein said frequency is greater than about 300 Hz.

10. The method of claim 1 wherein said adsorption current is at least twice as large as said diffusion current.

11. A method of evaluating the quality of a nucleic acid assay device comprising:

providing a nucleic acid assay device comprising an electrode surface wherein a plurality of nucleic acid probes are immobilized on said electrode surface;

quantitating said nucleic acid probes by detecting an electrical signal;

hybridizing a plurality of nucleic acid targets to said nucleic acid probes;

quantitating said nucleic acid targets by detecting an electrical signal;

correlating the quantity of said nucleic acid probes with the quantity of said nucleic acid targets to evaluate the quality of the nucleic acid assay device.

12. A method for performing an electrochemical assay, comprising:

providing an assay device comprising at least one electrode having polynucleotide capture probe attached;

providing a redox moiety in solution in contact with the electrode, wherein the redox moiety is capable of association with both the capture probe and with a polynucleotide target capable of hybridizing with the capture probe;

quantitating the capture probe on the electrode by measuring current associated with redox interaction with the electrode using cyclic voltammetry at a frequency greater than 75 Hz;

thereafter contacting the capture probe with a liquid to be analyzed for the presence of the polynucleotide target;

measuring a target current associated with interaction between the electrode and redox moiety associated with the polynucleotide target; and

calibrating the result of the target current measurement with reference to the quantity of polynucleotide capture probe on the electrode.

13. A method for performing an electrochemical assay, comprising the steps of:

providing an assay device having a capture probe attached to an electrode;

providing device-specific data reflective of the quantity of capture probe on the electrode, as measured electrochemically;

performing an electrochemical assay to detect an analyte, thereby generating a value reflective of the quantity of the analyte; and

providing a result of the assay reflecting interpretation of the result in light of the device-specific data.