SYSTEMS AND METHODS FOR POINT-OF-CARE AMPLIFICATION AND DETECTION OF POLYNUCLEOTIDES

• US 20100285479A1
• Filed: 05/13/2010
• Published: 11/11/2010
• Est. Priority Date: 02/22/2008
• Status: Active Grant

• Current Assignee: Vela Diagnostics Holding Pte. Ltd.
• Original Assignee: Great Basin Scientific
• Inventors: Jenison, Robert Delmar
• Granted Patent: US 8,637,250 B2
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: B01J 2219/00529 DNA chips
• CPC Class Codes: B01J 2219/00608 DNA chips
• CPC Class Codes: B01J 2219/00612 the surface being inorganic
• CPC Class Codes: B01J 2219/00626 Covalent
• CPC Class Codes: B01J 2219/00637 by coating it with another layer
• CPC Class Codes: B01J 2219/00722 Nucleotides
• CPC Class Codes: C12Q 1/6834 Enzymatic or biochemical coupling of nucleic acids to a solid phase
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 2521/513 Winding/unwinding enzyme, e.g. helicase
• CPC Class Codes: C12Q 2523/313 Irradiation, e.g. UV irradiation
• CPC Class Codes: C12Q 2527/101 Temperature
• CPC Class Codes: C12Q 2527/107 Temperature of melting, i.e. Tm
• CPC Class Codes: C12Q 2527/125 Specific component of sample, medium or buffer
• CPC Class Codes: C12Q 2537/101 Homogeneous assay format, e.g. one pot reaction
• CPC Class Codes: C12Q 2565/519 characterised by the capture moiety being a single stranded oligonucleotide

Abstract

Composition and methods for amplifying and detecting solution-state polynucleotide targets in a single device are described. In one aspect, a method for a coupled isothermal amplification and detection process utilizes a coated solid support, including a solid substrate, a cationic layer, and a plurality of target-specific probes attached to the coated solid support. Polynucleotide targets in the sample are amplified by an isothermal amplification process involving in situ hybridization onto the coated solid support. The entire process can be carried out with a high degree of specificity under low salt conditions in less than one hour. Further aspects of the present invention include methods for coupled hybridization/detection of polynucleotide targets, coated silicon biosensors optimized for use with the coupled detection systems to provide visual detection of polynucleotide targets under visible light conditions, and kits for practicing in the above described methods.

Claims

1. A method for detecting the presence or absence of a polynucleotide target in a sample, comprising:

a. providing a coated solid support comprising a solid support, a coating layer, and a plurality of target-specific probes attached to the coating layer;

b. applying to the coated solid support the sample and a reaction medium;

c. subjecting the sample to an isothermal amplification process capable of amplifying a polynucleotide target;

d. subjecting reaction products from the isothermal amplification process to conditions suitable for hybridizing amplified polynucleotide targets to the probes; and

e. detecting the presence or absence of polynucleotide targets bound to the probes.

3. The method of claim 1, wherein the isothermal amplification process comprises helicase-dependent amplification.

4. The method of claim 1, wherein the amplification and hybridization steps are performed concurrently in the reaction medium.

5. The method of claim 1, wherein the isothermal amplification and hybridization steps are performed at a monovalent cation concentration between about 10 mM and about 100 mM.

6. The method of claim 1, wherein each of the isothermal amplification, hybridization, and detection steps is performed on the coated solid support.

150. The method of claim 1, wherein the amplification step incorporates a label into the amplified polynucleotide targets.

151. The method of claim 150, wherein the detection step comprises binding an enzyme to the label and generating reaction products that are detectable on the surface of the coated solid support.

152. The method of claim 150, wherein the detection step comprises binding an anti-label antibody/enzyme conjugate to the label.

153. The method of claim 150, wherein the detection step comprises binding an enzyme to the label and generating precipitable reaction products that are detectable on the surface of the coated solid support under visible light.

154. The method of claim 1, wherein the solid support is formed from a member of the group consisting of silicon, plastic, glass, and membrane.

155. The method of claim 1, wherein the solid support comprises a silicon wafer or chip.

156. The method of claim 1, wherein the solid substrate is blocked or aged to reduce surface passivation of reaction components interfering with detection of polynucleotide targets bound to the probes.

157. The method of claim 1, wherein the coating layer comprises at least one polycationic polymer.

158. The method of claim 157, wherein the polycationic polymer is selected from one or more of the group consisting of polylysine, poly(lys-phe), poly(lys-tyr), poly(lys-trp), poly(arg-trp), and poly(arg-pro-tyr).

159. The method of claim 157, wherein the polycationic polymer is attached to the solid support.

160. The method of claim 1, wherein the coating layer comprises a compound selected from one or more of the group consisting of a cationic silane, a cationic siloxane, or a cationic derivative thereof.

161. The method of claim 1, wherein the coating layer comprises or is attached to a compound selected from one or more of the group consisting of aminopropyltrimethoxysilane, aminopropyltriethoxysilane, amino-functional organopolylsiloxanes, and amino-functional siloxane alkoxylates.

162. The method of claim 1, wherein the coating layer comprises an attachment layer.

163. The method of claim 1, wherein the plurality of target-specific probes are attached to an attachment layer comprising a coating of coupling agents deposited on the solid support surface.

164. The method of claim 1, wherein the plurality of target-specific probes comprise at least one modified oligonucleotide containing a structural element reducing binding of an isothermal amplification enzyme to an oligonucleotide bound to the polynucleotide target.

165. The method of claim 1, wherein the plurality of target-specific probes comprise at least one modified oligonucleotide containing a structural element reducing enzymatic denaturation of the oligonucleotide bound to the polynucleotide target.

166. The method of claim 1, wherein the plurality of target-specific probes comprise at least one probe having at least one terminus blocked to reduce recognition by an isothermal amplification enzyme.

167. The method of claim 1, wherein the plurality of target-specific probes comprise at least one probe modified or blocked to reduce recognition by a helicase.

168. The method of claim 1, wherein the plurality of target-specific probes comprise at least one probe comprising a backbone having at least one neutral charge.

169. The method of claim 1, wherein the plurality of target-specific probes comprise at least one probe comprising a methylphosphonate backbone.

170. The method of claim 1, wherein the plurality of target-specific probes comprise at least one probe comprising a peptide nucleic acid.

171. The method of claim 1, wherein the plurality of target-specific probes comprise at least one probe comprising a 2′

-O-methyl linkage.

172. The method of claim 1, wherein the plurality of target-specific probes comprise at least one probe comprising a locked nucleic acid.

173. The method of claim 1, wherein the sample comprises a purified polynucleotide or extract from an animal cell, microbial cell, or combinations thereof.

2. (canceled)

7-149. -149. (canceled)