Nanoscale transduction systems for detecting molecular interactions

• US 20050176029A1
• Filed: 10/20/2004
• Published: 08/11/2005
• Est. Priority Date: 10/20/2003
• Status: Abandoned Application

• Current Assignee: Regents of the University of California (University of California)
• Original Assignee: Regents of the University of California (University of California)
• Inventors: Zlatanovic, Sanja, Sullivan, Benjamin, Heller, Michael, Esener, Sadik, Dehlinger, Dietrich
• Application Number:
  US10/970,756
• Publication Number:
  US 20050176029A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: B82Y 10/00 Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
• CPC Class Codes: B82Y 15/00 Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
• CPC Class Codes: B82Y 30/00 Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: B82Y 5/00 Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
• CPC Class Codes: G01N 33/54346 Nanoparticles

Abstract

The present invention relates to nanoscale transduction systems that produce reversible signals to facilitate detection. In one respect, the invention relates to the analysis of molecular binding events using higher order signaling nanoscale constructs, or “nanomachines”, that allow nanostructures to be individually detectable, even in the midst of high background noise. Such systems are particularly useful for improving the performance of rare target detection methods, as well as being generally useful in any field in which sensitivity, discrimination and confidence in detection are important.

Claims

1. A method comprising binding a nanostructure and an associated structure to a target and reversibly altering interaction between the nanostructure, the associated structure and the target.

2. The method of claim 1, wherein the reversible alteration is in response to applied energy.

3. The method of claim 2, wherein the applied energy is an electric field.

4. The method of claim 2, wherein the applied energy is a DC field.

5. The method of claim 2, wherein the applied energy is an AC field.

6. The method of claim 2, wherein the applied energy is a capacitive field.

7. The method of claim 2, wherein the applied energy is thermal.

8. The method of claim 2, wherein the applied energy is electrical.

9. The method of claim 2, wherein the applied energy is chemical.

10. The method of claim 9, wherein the chemical energy is adenosine triphosphate (ATP) or nicotinamide adenine dinucleotide (NADH).

11. The method of claim 2, wherein the applied energy is photonic.

12. The method of claim 2, wherein the applied energy is magnetic.

13. The method of claim 2, wherein the applied energy is kinetic.

14. The method of claim 2, wherein the applied energy is acoustic.

15. The method of claim 14, wherein the applied energy is ultrasonic.

16. The method of claim 2, wherein the applied energy is microwave.

17. The method of claim 2, wherein the applied energy is radiative.

18. The method of claim 1, wherein the reversible alteration is deformation.

19. The method of claim 18, wherein the deformation is elastic, inelastic or plastic deformation.

20. The method of claim 1, wherein the reversible alteration is angular motion.

21. The method of claim 1, wherein the reversible alteration is a separation distance.

22. The method of claim 1, wherein the reversible alteration is a rotation.

23. The method of claim 1, wherein the reversible alteration is a linear displacement.

24. The method of claim 1, wherein the reversible alteration is helical motion.

25. The method of claim 1, wherein the reversible alteration is in response to shear force.

26. The method of claim 1, wherein the reversible alteration is in response to pressure.

27. The method of claim 1, wherein the interaction is resonant energy.

28. The method of claim 27, wherein the resonant energy is dipole coupling.

29. The method of claim 27, wherein the resonant energy is quadrapole coupling.

30. The method of claim 27, wherein the resonant energy is fluorescence resonance energy transfer.

31. The method of claim 1, wherein the interaction is plasmonic.

32. The method of claim 1, wherein the interaction is near field coupling.

33. The method of claim 1, wherein the interaction is photonic.

34. The method of claim 1, wherein the interaction is capacitive.

35. The method of claim 1, wherein the interaction is magnetic.

36. The method of claim 1, wherein the interaction is electrostatic.

37. The method of claim 1, wherein the method further comprises detecting a changed characteristic resulting from the interaction.

38. The method of claim 37, wherein the changed characteristic is a variation in luminescence.

39. The method of claim 37, wherein the changed characteristic is a variation in fluorescence.

40. The method of claim 37, wherein the changed characteristic is a variation in optical properties.

41. The method of claim 37, wherein the changed characteristic is color.

42. The method of claim 37, wherein the changed characteristic is a magnetic field.

43. The method of claim 37, wherein the changed characteristic is an electric field.

44. Then method of claim 37, wherein the changed characteristic is a surface enhanced Raman scattering (SERS) or Raman spectra.

45. The method of claim 1, wherein the reversibly altering interaction between the nanostructure, the associated structure and the target is spatially independent.

46. The method of claim 45, wherein the interaction occurs in a solution.

47. The method of claim 45, wherein the interaction occurs at a fixed location for which there is no a priori knowledge.

48. The method of claim 45, wherein the interaction occurs in a homogeneous assay.

49. The method of claim 45, wherein the interaction occurs in a heterogeneous assay.

50. The method of claim 45, wherein the interaction occurs in an in situ assay.

51. The method of claim 45, wherein the interaction occurs at a fixed location for which there is a priori knowledge.

52. The method of claim 51, wherein the method is performed on a microarray or nanoarray.

53. An apparatus comprising a nanostructure and an associated structure, wherein the nanostructure and the associated structure are adapted to reversibly interact with each other and a target.

54. The apparatus of claim 53, wherein the nanostructure is a quantum dot.

55. The apparatus of claim 53, wherein the nanostructure is a semiconductor nanoparticle.

56. The apparatus of claim 53, wherein the nanostructure is a photonic crystal.

57. The apparatus of claim 53, wherein the nanostructure is a metallic nanoparticle.

58. The apparatus of claim 53, wherein the nanostructure is a ceramic nanoparticle.

59. The apparatus of claim 53, wherein the nanostructure is a polymeric nanoparticle.

60. The apparatus of claim 53, wherein the nanostructure is a nanotube.

61. The apparatus of claim 53, wherein the associated structure is a quantum dot.

62. The apparatus of claim 53, wherein the associated structure is a semiconductor nanoparticle.

63. The apparatus of claim 53, wherein the associated structure is a photonic crystal.

64. The apparatus of claim 53, wherein the associated structure is a metallic nanoparticle.

65. The apparatus of claim 53, wherein the associated structure is a ceramic nanoparticle.

66. The apparatus of claim 53, wherein the associated structure is a polymeric nanoparticle.

67. The apparatus of claim 53, wherein the associated structure is a nanotube.

68. The apparatus of claim 53, wherein the associated structure further comprises a fluorophore, a quencher, a chromophore, a phycobillic protein, a lumiphore, a fluorescent protein.

69. The apparatus of claim 53, wherein the apparatus further comprises an interaction amplifying element.

70. The apparatus of claim 69, wherein the interaction amplifying element is attached to the nanostructure.

71. The apparatus of claim 69, wherein the interaction amplifying element is attached to the associated structure.

72. The apparatus of claim 69, wherein the interaction amplifying element is a pressure responsive element.

73. The apparatus of claim 69, wherein the interaction amplifying element is a displacement amplifying element.

74. The apparatus of claim 53, wherein the nanostructure has attached thereto a fluorescent donor, and wherein the associated structure further comprises a fluorescent quencher.

75. The apparatus of claim 53, wherein the nanostructure and the associated structure have attached thereto individual members of a fluorescent energy transfer (FRET) pair.

76. The apparatus of claim 53, wherein the nanostructure and the associated structure are adapted to reversibly and spatially independently interact with each other and a target.

77. The apparatus of claim 76, wherein the nanostructure and the associated structure are adapted to reversibly and spatially independently interact with each other and a target in solution.

78. The apparatus of claim 76, wherein the nanostructure and the associated structure are adapted to reversibly and spatially independently interact with each other and a target on a surface.

79. The apparatus of claim 78, wherein the surface is on a microarray or nanoarray.

80. A method comprising:

a. providing nanostructures, associated structures, and targets; and

b. detecting a temporally varying, spatially independent, information signal produced by the nanostructures, associated structures, and targets.

81. The method of claim 80, further comprising applying a driving force to the nanostructures, associated structures, and targets.

82. The method of claim 81, wherein the driving force is photonic.

83. The method of claim 81, wherein the driving force is electrical.

84. The method of claim 81, wherein the driving force is thermal.

85. The method of claim 81, wherein the driving force is magnetic.

86. The method of claim 81, wherein the driving force is periodic.

87. The method of claim 81, wherein the driving force is a series of impulses.

88. The method of claim 81, wherein the driving force is an impulse.

89. The method of claim 81, wherein the driving force is constant.

90. The method of claim 80, wherein the information signal is a variation in fluorescence of the nanostructure, associated structure, and target combinations.

91. The method of claim 80, wherein the information signal is a variation in color of the nanostructure, associated structure, and target combinations.

92. The method of claim 80, wherein the information signal is a variation in temperature of the nanostructure, associated structure, and target combinations.

93. The method of claim 80, wherein the information signal is a variation in electric field strength of the nanostructure, associated structure, and target combinations.

94. The method of claim 80, wherein the information signal is a variation in magnetic field strength of the nanostructure, associated structure, and target combinations.

95. The method of claim 80, wherein the information signal is a change in frequency of a characteristic of the nanostructure, associated structure, and target combinations.

96. The method of claim 80, further comprising processing the detected information signal to classify a molecular binding event.

97. The method of claim 80, further comprising processing the detected information signal utilizing neural networks.

98. The method of claim 80, further comprising processing the detected information signal utilizing Bayesian networks.

99. The method of claim 80, further comprising processing the detected information signal utilizing MAP detection.

100. The method of claim 80, further comprising applying a driving force that produces a reversibly altering interaction between a nanostructure, an associated structure, and a target comprising the information signal.

101. A system for detecting a target comprising:

a. a nanostructure, an associated structure, and the target, adapted to produce a reversibly altering interaction between the nanostructure, associated structure and target;

b. an input source adapted to impart energy to the nanostructure, associated structure, and target combination thereby producing the reversibly altering interaction; and

c. a detector configured to detect transduced output generated by the reversibly altering interaction.

102. The system of claim 101, wherein the imparted energy is photonic.

103. The system of claim 101, wherein the imparted energy is electrical.

104. The system of claim 101, wherein the imparted energy is thermal.

105. The system of claim 101, wherein the imparted energy is magnetic.

106. The system of claim 101, wherein the imparted energy is periodic.

107. The system of claim 101, wherein the imparted energy is a series of impulses.

108. The system of claim 101, wherein the imparted energy is an impulse.

109. The system of claim 101, wherein the imparted energy is constant.

110. The system of claim 101, wherein the transduced output is a variation in fluorescence of the nanostructure, associated structure, and target.

111. The system of claim 101, wherein the transduced output is a variation in color of the nanostructure, associated structure, and target.

112. The system of claim 101, wherein the transduced output is a variation in temperature of the nanostructure, associated structure, and target.

113. The system of claim 101, wherein the transduced output is a variation in a frequency of a characteristic of the nanostructure, associated structure, and target.

114. The system of claim 101, wherein the transduced output is a variation in electrical field strength of the nanostructure, associated structure, and target.

115. The system of claim 101, wherein the transduced output is a variation in magnetic field strength of the nanostructure, associated structure, and target.

116. A signaling nanostructure comprising at least one target binding region and at least one signal influencing region, wherein the signal influencing region has attached thereto a signal influencing element that alters a signaling characteristic of the nanostructure, and wherein the target binding region is selective for a predetermined target.

117. The signaling nanostructure of claim 116, wherein the signal influencing element is a signal inhibiting element.

118. The signaling nanostructure of claim 116, wherein the signaling nanostructure is fluorescent and the signal inhibiting element is a fluorescent quencher.

119. The signaling nanostructure of claim 116, wherein the target binding region and the signal influencing region are asymmetrically patterned on the surface of the signaling nanostructure.

120. The signaling nanostructure of claim 116, wherein the nanostructure further comprises only one target binding region.

121. The signaling nanostructure of claim 116, wherein the signal influencing element is a metallic nanoparticle.

123. The signaling nanostructure of claim 121, wherein the signal influencing element is a metallic nanoparticle.

122. A signaling nanostructure having at least one signal influencing region having attached thereto a signal influencing element that alters a signaling characteristic of the nanostructure, wherein the signal influencing element further comprises at least one target binding region having attached thereto a target binding element, and wherein the target binding element is selective for a predetermined target.

124. The signaling nanostructure of claim 122, wherein the target binding region further comprises a single target binding element attached thereto.

125. The signaling nanostructure of claim 122, wherein the target binding element is an oligonucleotide.

126. The signaling nanostructure of claim 122, wherein the target binding element is an antibody.

127. The signaling nanostructure of claim 122, wherein the target binding element is a polypeptide.

128. The signaling nanostructure of claim 122, wherein the signaling nanostructure and the signal influencing element are attached via the target binding element.

129. The signaling nanostructure of claim 122 having a first signal influencing element attached thereto, wherein the signal influencing element further comprises at least one target binding region, and wherein the signaling nanostructure further comprises a second signal influencing element attached thereto.

130. The signaling nanostructure of claim 122, wherein the first and the second signal influencing elements are metallic nanoparticles.

131. A kit comprising:

a. a first signaling nanostructure having a first metallic nanoparticle attached thereto, wherein the first metallic nanoparticle further comprises at least one first target binding region having attached thereto a first target binding element, and wherein the first target binding element is selective for a predetermined target; and

b. a second metallic nanoparticle comprising at least one second target binding region having attached thereto a second target binding element, and wherein the second target binding element is selective for the same predetermined target.

132. The kit of claim 131, wherein the first and second target binding elements are antibodies.

133. The kit of claim 131, wherein the first and second target binding elements are oligonucleotides.

134. The kit of claim 131, wherein the first and second target binding elements are polypeptides.

135. The kit of claim 131, wherein the first and second metallic nanoparticle are attached via a tethering group.

136. The kit of claim 131, wherein the tethering group is a synthetic polymer, a single stranded nucleic acid, a fatty acid, a glycosaminoglycan or a polypeptide.

137. A method comprising the steps of:

a. binding a nanostructure to a target;

b. binding an associated structure to the target;

c. reversibly altering an interaction between the nanostructure, the associated structure and the target to produce information; and

d. detecting the information.

138. The method of claim 137, wherein the target is a nucleic acid.

139. The method of claim 137, wherein the target is a protein.

140. The method of claim 137, wherein the target is an inorganic surface.

141. The method of claim 137, wherein the target is genomic nucleic acid.

142. The method of claim 137 further comprising detecting a target in a biological sample.

143. The method of claim 137, wherein the biological sample is a cell or tissue sample on a microscope slide.

144. The method of claim 143, wherein the target is a nucleic acid.

145. The method of claim 137, wherein the nanostructure further comprises a first target binding region having a target binding element attached thereto that is selective for a predetermined target;

and wherein the associated structure further comprises a second target binding region having attached thereto a second target binding element that is selective for the same predetermined target.

146. The method of claim 145, wherein the first and second target binding elements are oligonucleotides.

147. The method of claim 137, wherein the target is an antigen, and wherein the first and second target binding elements are antibodies that bind to the antigen.

148. The method of claim 137 adapted to be performed in a solution, and wherein step c. is performed without removing the nanostructure or the associated structure from the solution.

149. A metallic nanoparaticle having attached thereto a signaling element and a target binding element.

150. The metallic nanoparticle of claim 149, wherein the signaling element is a quantum dot.

151. The metallic nanoparticle of claim 149, wherein the signaling element is a fluorophore.

152. The metallic nanoparticle of claim 149, wherein the signaling element is a FRET donor or a FRET acceptor.

153. The metallic nanoparticle of claim 149, wherein the target binding element is an antibody.

154. The metallic nanoparticle of claim 149, wherein the target binding element is a nucleic acid.

155. The metallic nanoparticle of claim 149, wherein the target binding element is a polypeptide.

156. A method for identifying a target nucleic acid molecule in a sample, the method comprising:

a. contacting the target nucleic acid molecule with a first nucleic acid probe comprising a signaling element, wherein the first nucleic acid probe hybridizes to the target molecule;

b. contacting the target nucleic acid with a second nucleic acid probe comprising a signal inhibiting element, wherein the second probe hybridizes to the target nucleic acid molecule such that the signal inhibiting element is in proximity to the signaling element thereby reducing the signal associated with the signaling element;

c. applying a pulsed electric field to a nucleic acid complex formed by the target nucleic acid and hybridized probes, wherein the pulsed electric field periodically interrupts the ability of the signal inhibiting element to reduce the signal associated with the signaling element thereby producing an oscillating signal; and

d. detecting the oscillating signal.

157. The method of claim 156, wherein the signaling element is a fluorescent label.

158. The method of claim 156, wherein the signal inhibiting element is a fluorescent quencher.

159. The method of claim 157, wherein the fluorescent label comprises a donor group for fluorescent energy transfer (FRET).

160. The method of claim 158, wherein the fluorescent quencher comprises an acceptor group for fluorescent energy transfer (FRET).

161. The method of claim 156, wherein the application of the electric field results in a change in distance between the signaling element and the signal inhibiting element.

162. The method of claim 156, wherein the target nucleic acid molecule is DNA or RNA.

163. The method of claim 156, wherein the first nucleic acid probe is DNA or RNA.

164. The method of claim 156, wherein the second nucleic acid probe is DNA or RNA.

165. The method of claim 156, wherein the target nucleic acid molecule is associated with a pathological condition or genetic alteration.

166. The method of claim 156, wherein the sample comprises a plurality of non-target nucleic acid molecules.

167. The method of claim 156, wherein the sample comprises a plurality of target nucleic acid molecules.

168. The method of claim 156, wherein the pulsed electric field is alternating current or direct current.

169. The method of claim 156, wherein the signaling element is a nanoparticle.

170. The method of claim 169, wherein the nanoparticle is selected from the group consisting of a polymer bead, a quantum dot and a gold particle.

171. The method of claim 156, wherein the sample is associated with a solid support.

172. The method of claim 171, wherein the solid support is an array.

173. The method of claim 172, wherein the array is a microarray.

174. The method of claim 156, further comprising amplifying the target nucleic acid molecule.

175. A diagnostic profile produced by the method of claim 156.

176. The diagnostic profile of claim 175, wherein the diagnostic profile is correlated with a wild-type state, a pathological condition, or a genetic alteration.