초록 ▼

This invention pertains to the design, fabrication, and uses of an electronic system which can actively carry out and control multi-step and multiplex reactions in macroscopic or microscopic formats. In particular, these reactions include molecular biological reactions, such as nucleic acid hybridiz

This invention pertains to the design, fabrication, and uses of an electronic system which can actively carry out and control multi-step and multiplex reactions in macroscopic or microscopic formats. In particular, these reactions include molecular biological reactions, such as nucleic acid hybridizations, nucleic acid amplification, sample preparation, antibody/antigen reactions, clinical diagnostics, combinatorial chemistry and selection, drug screening, oligonucleotide and nucleic acid synthesis, peptide synthesis, biopolymer synthesis and catalytic reactions. A key feature of the present invention is the ability to control the localized concentration of two or more reaction-dependant molecules and their reaction environment in order to greatly enhance the rate and specificity of the molecular biological reaction.

대표청구항 ▼

1. A device for the modulation of a reaction comprising:a first buffer reservoir containing a first buffer and a first charged entity, wherein the first buffer has an initial conductance less than 1000 μS/cm;a second buffer reservoir separated from the first buffer reservoir containing a secon

1. A device for the modulation of a reaction comprising:a first buffer reservoir containing a first buffer and a first charged entity, wherein the first buffer has an initial conductance less than 1000 μS/cm;a second buffer reservoir separated from the first buffer reservoir containing a second buffer comprising a second charged entity, wherein the second charged entity has a charge opposite that of the first charged entity, the second charged entity modulates the specific reaction between the specific binding entity and the first charged entity;a conductive semipermeable matrix contained in a non-conductive support material, the conductive semipermeable matrix disposed between and fluidically connecting the first buffer reservoir and the second buffer reservoir;a first electrode linked to a power source and located in the first buffer reservoir and contacting the first buffer; anda second electrode linked to the power source and located in the second buffer reservoir and contacting the second buffer; anda specific binding entity which reacts specifically with the first charged entity and which is physically fixed on, in, or adjacent to the semipermeable matrix. 2. The device of claim 1 comprising a common first buffer reservoir connected through a plurality of semipermeable matrices to a common second buffer reservoir. 3. The device of claim 1 further comprising a plurality of first buffer reservoirs connected through a plurality of semipermeable matrices to a common second buffer reservoir. 4. The device of claim 1 further comprising a plurality of first buffer reservoirs connected through a plurality of semipermeable matrices to a plurality of second buffer reservoirs. 5. The device of claim 1 further comprising a common first buffer reservoir connected through a plurality of semipermeable matrices to a plurality of second buffer reservoirs. 6. The device of claim 1 comprising a common first electrode and a common second electrode. 7. The device of claim 1 further comprising a plurality of first electrodes and a common second electrode. 8. The device of claim 1 further comprising a common first electrode and a plurality of second electrodes. 9. The device of claim 1 further comprising a plurality of first electrodes and a plurality of second electrodes. 10. The device of claim 1 wherein the specific binding entity is attached through a covalent or non-covalent bond to a portion of the semipermeable matrix comprising at least the portion of the semipermeable matrix at or around the first-buffer-side of the semipermeable matrix. 11. The device of claim 1 wherein the initial conductance of the first buffer is in the range of 0.1 to 250 μS/cm. 12. The device of claim 1 wherein the initial conductance of the first buffer is in the range of 0.1 to 100 μS/cm. 13. The device of claim 1 wherein the initial conductance of the first buffer is in the range of 0.1 to 50 μS/cm. 14. The device of claim 1 wherein the concentration of the buffer species in the first buffer is in the range of 10 mM to 300 mM. 15. The device of claim 1 wherein the concentration of the buffer species in the first buffer is in the range of 25 mM to 200 mM. 16. The device of claim 1 wherein the ratio of the initial concentration of the second charged entity in the first buffer to the initial concentration of the second charged entity in the second buffer is less than 1:1. 17. The device of claim 1 wherein the ratio of the initial concentration of the second charged entity in the first buffer to the initial concentration of the second charged entity in the second buffer is less than 1:10. 18. The device of claim 1 wherein the ratio of the initial concentration of the second charged entity in the first buffer to the initial concentration of the second charged entity in the second buffer is less than 1:100. 19. The device of claim 1 wherein the ratio of the initial concentration of the second charged entity in the first buffer to the initia l concentration of the second charged entity in the second buffer is less than 1:1000. 20. The device of claim 1 wherein the first buffer comprises a zwitterionic buffer. 21. The device of claim 20 wherein the zwitterionic buffer is chosen from the group consisting of β-alanine, taurine, cysteine, histidine, methylhistidine, lysine, γ-amino butyric acid, glycine, ε-amino caproic acid, and carnosine buffers. 22. The device of claim 20 wherein the zwitterionic buffer is a histidine buffer. 23. The device of claim 1 wherein the second charged entity is more than one charged species. 24. The device of claim 23 wherein the each of the charged species comprising the second charged entity has approximately the same rate of migration through the semipermeable matrix when an electric potential is applied across the semipermeable matrix. 25. The device of claim 23 wherein the each charged species comprising the second charged entity has a significantly different rate of migration through the semipermeable matrix when an electric potential is applied across the semipermeable matrix. 26. The device of claim 1 wherein the first charged entity is more than one charged species. 27. The device of claim 1 wherein the first charged entity is a nucleic acid polymer. 28. The device of claim 27 wherein the specific binding entity is a nucleic acid polymer. 29. The device of claim 1 wherein the specific binding entity is a polypeptide. 30. The device of claim 1 wherein the first charged entity is a polypeptide. 31. The device of claim 1 wherein the second charged entity is a cation. 32. The device of claim 31 wherein the cation is chosen from the group consisting of positively charged amino acids, positively charged oligopeptides, metal cations, organically chelated metal cations, positively charged detergents, and positively charged amines. 33. The device of claim 31 wherein the cation is protonated histidine. 34. The device of claim 33 wherein the cation is selected from the group consisting of Na + , K + , Ag + , Cu + , Mg +2 , Ca +2 , Zn +2 , Cu +2 , Ni +2 , Co +2 , Fe +2 , Se +2 , Mn +2 , Al +3 , Cr +3 , Fe +3 , Co +3 , Mn +4 and Se +4 . 35. The device of claim 1 wherein all first electrodes and second electrodes are connected to a power source which controls the voltage of the electrodes in parallel. 36. The device of claim 9 wherein the plurality of first electrodes and second electrodes are connected to a power source which controls the voltage of the electrodes in series. 37. The device of claim 9 wherein the plurality of first electrodes and second electrodes are connected to a power source which controls the voltage of the electrodes independently. 38. The device of claim 9 wherein the plurality of first electrodes and second electrodes are connected to a power source which controls the current through the electrodes in parallel. 39. The device of claim 9 wherein the plurality of first electrodes and second electrodes are connected to a power source which controls the current through the electrodes in series. 40. The device of claim 9 wherein the plurality of first electrodes and second electrodes are connected to a power source which controls the current through the electrodes independently. 41. The device of claim 9 wherein the plurality of first electrodes and second electrodes are connected to a power source which controls the power to the electrodes in parallel. 42. The device of claim 9 wherein the plurality of first electrodes and second electrodes are connected to a power source which controls the power to the electrodes in series. 43. The device of claim 9 wherein the plurality of first electrodes and second electrodes are connected to a power source which controls the power to the electrodes independently. 44. The device of claim 1 wherein the first electrodes and second electrodes comprise a material chosen from the group consisting of as aluminum, gold, silver, tin, platinum, titanium, cop per, palladium, iridium, conductive polymers, conductive metal alloys, and carbon. 45. The device of claim 1 wherein the first electrodes and second electrodes comprise platinum. 46. The device of claim 1 wherein the semipermeable matrix is contained within a support material selected from the group consisting of glass, polymers, rubber, ceramics, and combinations thereof. 47. The device of claim 1 wherein the semipermeable matrix is contained within a support material that produces a low background signal. 48. The device of claim 46 wherein the support material is a black-colored organic polymer material with a low fluorescence signal. 49. The device of claim 46 wherein the support material is a low-fluorescence silica glass. 50. The device of claim 1 wherein the semipermeable matrix comprises a single layer of material. 51. The device of claim 50 wherein the single layer of material is substantially uniform throughout the semipermeable matrix. 52. The device of claim 50 wherein the single layer of material is chemically modified at or near the first-buffer-side surface of the semipermeable matrix for the attachment of a specific binding entity. 53. The device of claim 50 wherein the single layer of material consists of a composite material. 54. The device of claim 1 wherein the semipermeable matrix comprises a plurality of material layers. 55. The device of claim 54 wherein the semipermeable matrix comprises a membrane layer. 56. The device of claim 55 wherein the membrane has an pore size limit which is slightly greater than the radius of gyration of the first charged entity. 57. The device of claim 55 wherein the membrane has a molecular weight cutoff between 1 kilodalton and 10 kilodaltons. 58. The device of claim 55 wherein the membrane has a molecular weight cutoff between 3 kilodaltons and 5 kilodaltons. 59. The device of claim 55 wherein the membrane has a pore size limit which is between 1 nm and 10 nm. 60. The device of claim 55 wherein the membrane has a charged surface. 61. The device of claim 60 wherein the membrane has a negatively charged surface. 62. The device of claim 60 wherein the membrane has a positively charged surface. 63. The device of claim 55 wherein the membrane provides sites for the attachment of the specific binding entity. 64. The device of claim 1 wherein the semipermeable matrix comprises a sedimentation layer. 65. The device of claim 64 wherein the sedimentation layer is bounded on only one side by another layer of the semipermeable matrix. 66. The device of claim 64 wherein the sedimentation layer comprises a material chosen from the group consisting of metallic microspheres, silica, chromatography resins, and polymer microspheres. 67. The device of claim 1 wherein the semipermeable matrix comprises at least one material chosen from the group consisting of organic hydrogels, sol-gels, aero-gels, fritted glass, porous glass, chromatographic resins, porous silicon, cross linked polymers, and membranes. 68. The device of claim 67 wherein the organic hydrogel is chosen from the group consisting of polyacrylamide gels and carbohydrate gels. 69. The device of claim 67 wherein the chromatographic resin is chosen from the group consisting of charged chromatographic resins and size-exclusion pore chromatographic resins. 70. The device of claim 69 wherein the charged chromatographic resin is an anionic chromatographic resin. 71. The device of claim 69 wherein the charged chromatographic resin is a cationic chromatographic resin. 72. The device of claim 67 wherein the membrane is chosen from the group consisting of cellulose membranes, nitrocellulose membranes, nylon membranes, chitosan membranes, polycarbonate membranes, and DEAE membranes. 73. The device of claim 1 further comprising a microprobe at the first-buffer-side surface of the semipermeable matrix which is capable of detecting the concentration of the second charged entity at and around the first-buffer-side surface of the semipermeable mat rix. 74. The device of claim 73 wherein the microprobe measures pH at and around the first-buffer-side surface of the semipermeable matrix. 75. The device of claim 73 wherein the microprobe measures conductance at and around the first-buffer-side surface of the semipermeable matrix. 76. The device of claim 73 wherein the microprobe is connected to a microprocessor which controls the first electrodes and second electrodes. 77. The device of claim 1 further comprising a microprobe at the first-buffer-side surface of the semipermeable matrix which is capable of detecting the concentration of the product of a reaction between the first charged entity, the second charged entity, and the specific binding entity, at and around the first-buffer-side surface of the semipermeable matrix. 78. The device of claim 77 wherein the microprobe measures pH at and around the first-buffer-side surface of the semipermeable matrix. 79. The device of claim 77 wherein the microprobe measures conductance at and around the first-buffer-side surface of the semipermeable matrix. 80. The device of claim 77 wherein the microprobe is connected to a microprocessor which controls a voltage regulator which controls the first electrodes and second electrodes. 81. The device of claim 1 wherein the second buffer reservoir is a common second buffer reservoir for all semipermeable matrices, and the second electrode is a common second electrode for all semipermeable matrices, and wherein the device further comprises a set of baffles in the second buffer reservoir. 82. The device of claim 1 wherein the semipermeable matrix is so composed as to inhibit free diffusion of molecules between the first and second buffer reservoirs. 83. The device of claim 1 wherein the semipermeable matrix is so composed that there is little or no migration of the first charged entity through the semipermeable matrix into the second buffer reservoir during the time necessary to complete the biochemical reaction in the absence or presence of an electric potential across the semipermeable matrix. 84. The device of claim 1 wherein the semipermeable matrix is so composed that there is little or no migration of the second charged entity through the semipermeable matrix into the first buffer reservoir during the time necessary to complete the biochemical reaction in the absence of an electric potential across the semipermeable matrix, but so that there is controlled migration of the second charged entity through the semipermeable matrix in the presence of an electric potential across the semipermeable matrix. 85. The device of claim 1 wherein the first electrode is negatively biased. 86. The device of claim 1 wherein the second electrode is positively biased.