IP Library Granted Patent US 8,294,122
Granted Patent B2
US 8,294,122 · App. 12/400,321 · Granted Oct 23, 2012

Method for fluorescence analysis and fluorescence analyzer

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Quick Facts
Patent No.
US 8,294,122
App. No.
12/400,321
Granted
Oct 23, 2012
Kind
B2
Abstract

The present invention aims at reducing background noise derived from a substance that is present in the vicinity of a target substance such as a DNA and protein and attached to the surface of a substrate without an effect on a fluorescent dye labeling the target substance. The substrate that has a probe and is capable of interacting with the target substance is irradiated with noise removing light such that an evanescent field is generated on the surface of the substrate. A target substance and a foreign particle, which are non-specifically stuck to the surface of the substrate, are decomposed by the evanescent field generated by the irradiation with the noise removing light. The evanescent field present near the surface of the substrate has almost no effect on the probe. It is possible to reduce the background noise derived from the substance that is present in the vicinity of the target substance and attached to the surface of the substrate and suppress effects on the probe and the target substance interacting with the probe.

Claims (32)

1. A fluorescence analyzer comprising:

a substrate including a probe configured to interact with a target substance;

an excitation light irradiation optical system configured to irradiate the target substance or the probe with excitation light;

a fluorescence detection optical system configured to detect fluorescence generated by the irradiation with the excitation light from the excitation light irradiation optical system; and

a noise removing optical system comprising a noise removing source, wherein the noise removing optical system is configured to irradiate the substrate with noise removing light, wherein the target substance and a foreign particle are non-specifically stuck to the surface of the substrate, and the target substance and the foreign particle are decomposed by the noise removing light, under a condition that an evanescent field is generated on the surface of the substrate, wherein:

the probe is present outside the evanescent field, and inside an area irradiated with excitation light, and

the excitation light irradiation optical system is configured to irradiate the target substance or the probe with excitation light after the noise removing optical system irradiates the substrate with noise removing light.

2. The fluorescence analyzer according to claim 1 , wherein the excitation light irradiation optical system is configured to irradiate the substrate with the excitation light, under a condition that an evanescent field is generated on the surface of the substrate.

3. The fluorescence analyzer according to claim 2 , wherein the excitation light is visible light, and the noise removing light is ultraviolet light.

4. The fluorescence analyzer according to claim 1 , wherein a spacer is present on the surface of the substrate and provided with the probe.

5. The fluorescence analyzer according to claim 1 , wherein a support body provided with the probe faces the surface of the substrate.

6. The fluorescence analyzer according to claim 1 , wherein the

substrate has a nano-aperture, and the noise removing optical system irradiates the nano-aperture with the noise removing light to generate an evanescent field on the surface of the substrate.

7. The fluorescence analyzer according to claim 1 , wherein the probe is a deoxyribonucleic acid, a ribonucleic acid, an aptamer, a gene, a nucleosome, a chromatin, a chromosome, a nucleoid, a cell membrane, a cell wall, a virus, an antigen, an antibody, a lectin, a hapten, a receptor, an enzyme, a peptide, a glycosphingolipid or a sphingolipid.

8. The fluorescence analyzer according to claim 1 , wherein the target substance is a deoxyribonucleic acid, a ribonucleic acid, an aptamer, an antigen, an antibody, a deoxyribonucleoside triphosphate, or a ribonucleoside triphosphate.

9. The fluorescence analyzer according to claim 1 , wherein the target substance is a monomer of a fluorescent-labeled nucleotide or an oligomer of a fluorescent-labeled nucleotide, the probe is a nucleic acid synthesis enzyme or a nucleic acid molecule, the probe interacts with the target substance to generate a nucleic acid chain containing the nucleotide, and fluorescence emitted by a fluorescent dye contained in the nucleotide is detected to acquire information on a nucleic acid sequence.

10. A fluorescence analyzer comprising:

an optically transparent substrate having a spacer comprising a probe;

a reaction tank configured to hold, on the surface of the optically transparent substrate, a solution containing a target substance configured to interact with the probe;

a prism in direct contact with or in indirect contact with the optically transparent substrate;

a first light source configured to emit excitation light that is laser light; and

a noise removing light source configured to emit ultraviolet light that is laser light, wherein:

the excitation light is incident on the prism and totally reflected by the surface of the optically transparent substrate to generate an evanescent field in a region in which the probe is present, and the ultraviolet light is incident on the prism and totally reflected by the surface of the optically transparent substrate to generate an evanescent field in a region in which the probe is not present, and

the first light source is configured to emit the excitation light after the ultraviolet light is emitted.

11. A fluorescence analyzer comprising:

a substrate having a probe configured to interact with a target substance;

a first reaction tank configured to hold a solution on the surface of the substrate;

a noise removing optical system comprising a noise removing source, wherein the noise removing optical system is configured to irradiate the substrate provided in the first reaction tank with a noise removing light, under a condition that an evanescent field is generated on the surface of the substrate;

a second reaction tank configured to hold, on the surface of an optically transparent substrate, a solution containing the target substance capable of interacting with the probe;

an excitation light irradiation optical system configured to irradiating the substrate provided in the second reaction tank with excitation light; and

a fluorescence detection optical system configured to detect fluorescence generated by the irradiation with the excitation light,

wherein the excitation light irradiation optical system is configured to irradiate the target substance or the probe with excitation light after the noise removing optical system irradiates the substrate with noise removing light.

Assignments (1)
CHANGE OF NAME AND ADDRESS Recorded Mar 30, 2020
From: HITACHI HIGH-TECHNOLOGIES CORPORATION
To: HITACHI HIGH-TECH CORPORATION
Reel/Frame 052259/0227 →