METHOD FOR IDENTIFYING AND QUANTIFYING ORGANIC AND BIOCHEMICAL SUBSTANCES
A method for identifying and quantifying organic or biochemical substances in a fluid medium using a nanogap sensor is disclosed. A nanogap sensor with two electrodes of different materials is used, a respective probe molecule is bonded to each electrode and the free remainder of the probe molecules have at least one bondable group with specificity to a substance or analyte. The analyte has at least two binding sites and passes selectively out of the fluid medium, binds to the free ends of the probe molecules to form a bridge, modifying the impedance between the electrodes.
1 . (canceled)
2 . A method of detecting an analyte, the method comprising:
exposing a closed circuit to the analyte in a fluid medium, the closed circuit comprising: a first electrode; a second electrode spaced apart from the first electrode by a nanogap; a first affinity probe bonded to the first electrode; a second affinity probe bonded to the second electrode; and a single-stranded DNA oligonucleotide bridge molecule bonded at each end to the first and second affinity probes, bridging the nanogap;
binding the analyte to the first affinity probe while correspondingly dissolving the bond between the first affinity probe and an end of the single-stranded DNA oligonucleotide bridge molecule, thereby opening the closed circuit; and
observing a resulting change in impedance from the opening of the closed circuit, the change in impedance indicating the presence of the analyte in the fluid medium.
3 . The method of claim 2 , wherein the first electrode comprises diamond and the second electrode comprises silicon.
4 . The method of claim 3 , wherein the bond between the diamond electrode and the first affinity probe comprises a bifunctional crosslink between an amino group of a phenylamino moiety immobilized on the diamond electrode and an amino group present on the first affinity probe, the bifunctional cross-link comprising the two amino groups and a phenylene di-isothiocyanate cross-linker.
5 . The method of claim 2 , wherein the first electrode comprises silicon and the second electrode comprises diamond.
6 . The method of claim 5 , wherein the bond between the diamond electrode and the second affinity probe comprises a bifunctional crosslink between an amino group of a phenylamino moiety immobilized on the diamond electrode and an amino group present on the second affinity probe, the bifunctional cross-link comprising the two amino groups and a phenylene di-isothiocyanate cross-linker.
7 . The method of claim 2 , wherein the closed circuit further comprises at least one helper oligonucleotide bonded to the single-stranded DNA oligonucleotide bridge molecule initially bridging the nanogap in the closed circuit.
8 . The method of claim 2 , wherein the nanogap measures from about 20 nm to about 70 nm.
9 . The method of claim 2 , wherein the single-stranded DNA oligonucleotide bridge molecule initially bridging the nanogap in the closed circuit comprises at least one point mutation resulting in weaker binding between the single-stranded DNA oligonucleotide bridge molecule and the first affinity probe relative to binding between the analyte and the first affinity probe.
10 . The method of claim 2 , wherein the closed circuit further comprises an external reference electrode.
11 . The method of claim 2 , wherein the first and second electrodes are electrically connected to a measuring device.
12 . The method of claim 11 , wherein the measuring device is capable of measuring DC voltage offset impedance.
13 . The method of claim 2 , further comprising equilibrating the electrodes with a buffer that does not comprise the analyte, prior to exposing the closed circuit to the analyte in the fluid medium.