초록 ▼

A method of detecting the presence of an analyte, such as a target nucleic acid sequence, protein sequence or small molecule, which can also be employed to detect the formation of duplex structures, is disclosed. The method can comprise nucleic acids, proteins and small molecules, employing photoele

A method of detecting the presence of an analyte, such as a target nucleic acid sequence, protein sequence or small molecule, which can also be employed to detect the formation of duplex structures, is disclosed. The method can comprise nucleic acids, proteins and small molecules, employing photoelectrochemically active nanoparticles, branched polymers or other structures that carry photoelectrochemically active molecules capable of generating a photocurrent when excited by light in the presence of an electric field is disclosed. The method can be employed to detect hybridization on an array and can be employed in sequencing, mutational analysis (for example, single nucleotide polymorphisms and other variations in a population) and for monitoring gene expression by analysis of the level of expression of messenger RNA extracted from a cell. The method is applicable to the detection of antibody binding or other protein binding for analyte detection in an array format. The creation of an array addressable by light is disclosed.

대표청구항 ▼

What is claimed is: 1. A method of detecting a plurality of different target analytes comprising: (a) providing a conductive support comprising a single electrode, wherein said single electrode comprises an array comprising a plurality of different probes, wherein each of the plurality of different

What is claimed is: 1. A method of detecting a plurality of different target analytes comprising: (a) providing a conductive support comprising a single electrode, wherein said single electrode comprises an array comprising a plurality of different probes, wherein each of the plurality of different probes is attached at one of a plurality of discrete positions; (b) contacting the plurality of different probes with a plurality of different target analytes, wherein each of the plurality of different target analytes is selected from the group consisting of a single stranded DNA oligomer, a single stranded RNA oligomer, a peptide nucleic acid analog, double stranded DNA, an antibody, a polypeptide, a peptide, a target analyte that is reverse transcribed from a nucleic acid sequence, a target analyte comprising intact genomic DNA, a target analyte comprising fragmented genomic DNA, mRNA, a PCR product and an OLA product, further wherein each of the plurality of different target analytes comprises a nanoparticle comprising a photoelectrochemically active moiety, thereby forming a support comprising a plurality of different target analytes attached thereto; (c) irradiating one of the plurality of discrete positions with light individually, thereby generating a photoelectric current between a photoelectrochemically active moiety and the conductive support if a target analyte is present; (d) measuring the photoelectric current to determine the presence or the amount of a target analyte at the discrete position irradiated; and (e) repeating the irradiating and measuring steps for each of a plurality of discrete positions on the support sequentially, thereby determining the presence or the amount of each of a plurality of different target analytes. 2. The method of 1, wherein the nanoparticle comprises a material selected from the group consisting of a metal, a metal oxide, a ceramic, a semiconductor, a dendrimer and an organic polymer. 3. The method of claim 2, wherein the nanoparticle comprises a material selected from the group consisting of titanium, titanium dioxide, tin, tin oxide, silicon, silicon dioxide, iron, ironIII oxide, silver, gold, copper, nickel, aluminum, steel, indium, indium tin oxide, fluoride-doped tin, ruthenium oxide, germanium cadmium selenide, cadmium sulfide and titanium alloy. 4. The method of claim 1, wherein the support comprises a material selected from the group consisting of titanium dioxide, tin oxide, silicon, ironIII oxide, silver, nickel, gold, indium tin oxide, conductive polymers, metals, semiconductors and plastics coated with a conductant. 5. The method of claim 1, wherein each of the plurality of different target analytes is an oligonucleotide whose sequence is determined by surface binding or hybridization. 6. The method of claim 5, wherein each of the plurality of different target analytes further comprises a tag sequence. 7. The method of claim 1, wherein the photoelectrochemically active moiety comprises a ruthenium center. 8. The method of claim 1, wherein the light is provided by a light source selected from the group consisting of a tungsten halogen light source, a xenon arc lamp and a laser. 9. The method of claim 1, wherein the irradiating is by rastering. 10. The method of claim 1, wherein the irradiating is performed in the presence of a redox mediator. 11. The method of claim 1, wherein each of the plurality of different probes is selected from the group consisting of a single stranded DNA oligomer, a single stranded RNA oligomer, a peptide nucleic acid analog, double stranded DNA, an antibody, a polypeptide, a peptide, a target analyte that is reverse transcribed from a nucleic acid sequence, a target analyte comprising intact genomic DNA, a target analyte comprising fragmented genomic DNA, mRNA, a PCR product and an OLA product. 12. The method of claim 11, wherein each of the plurality of different probes further comprises a tag sequence. 13. The method of claim 1, further comprising passivating the support with a passivation moiety before contacting the plurality of different target analytes with the plurality of different probes under hybridization conditions. 14. The method of claim 13, wherein the passivation moiety comprises a moiety selected from the group consisting of silyl chloride, a sol gel, polyethylene glycol, a thiol, a siloxane, an organic polymer, a carboxylate and combinations thereof. 15. The method of claim 1, further comprising contacting the support with a secondary component after contacting the plurality of different target analytes with the plurality of different probes under hybridization conditions. 16. The method of claim 15, wherein the secondary component is a photoelectrochemically active moiety. 17. The method of claim 1, wherein the providing comprises contacting the plurality of different probes with the plurality of different target analytes under hybridization conditions and further wherein the nanoparticle comprises a central component and a plurality of photoelectrochemically active moieties. 18. The method of claim 17, wherein each of the plurality of different target analytes is selected from the group consisting of an mRNA sequence derived from a sample to be monitored for gene expression and a cDNA sequence derived from a sample to be monitored for gene expression. 19. The method of claim 18, wherein one of the plurality of different probes comprises a gene of interest. 20. The method of claim 18, wherein the presence of a photoelectric current is indicative of duplex formation and duplex formation is indicative of gene expression. 21. The method of claim 1, wherein one or more of the plurality of different probes comprises or is suspected to comprise a mutation to be detected, and the plurality of different probes is contacted with the plurality of different target analytes under hybridization conditions. 22. The method of claim 1, wherein the nanoparticle comprises a central component comprising gold or titanium dioxide, said central component having attached thereto a plurality of thiolated [Ru(bpy)3]2+ groups. 23. The method of claim 1, wherein each of the plurality of different target analytes is isolated from a cell or is chemically or enzymatically synthesized.