ELECTROCHEMICAL CELLULAR CIRCUITS

Abstract

Disclosed herein is a method of measuring a cell population, the method including culturing a cell population in a growth medium, wherein the cell population includes a cell strain including a control gene and a promoter sequence; positioning first and second electrodes in contact with the growth medium, wherein the first and second electrodes are connected to different terminals of an electrical source; applying an electrical signal between the two electrodes; measuring an electrical parameter of the growth medium as a function of time; and determining information about the cell population based upon the measured electrical parameter.

Description

Claims

1. A method of measuring a cell population, the method comprising: culturing a cell population in a growth medium, wherein the cell population comprises a cell strain comprising a control gene and a promoter sequence;positioning first and second electrodes in contact with the growth medium, wherein the first and second electrodes are connected to different terminals of an electrical source;applying an electrical signal between the two electrodes;measuring an electrical parameter of the growth medium as a function of time; anddetermining information about the cell population based upon the measured electrical parameter.

2. The method of claim 1, wherein the electrical parameter comprises an electrical admittance of the growth medium.

3. The method of claim 1, wherein the electrical parameter comprises an electrical impedance of the growth medium.

4. The method of claim 1, wherein the electrical parameter comprises a conductance of the growth medium.

5. The method of claim 1, wherein the electrical parameter comprises a resistance of the growth medium.

6. The method of claim 1, wherein applying the electrical signal comprises applying an electrical potential difference between the two electrodes.

7. The method of claim 1, wherein the cell population comprises one or more different bacterial strains.

8. The method of claim 1, wherein the cell population comprises one or more different yeast strains.

9. The method of claim 1, wherein the cell population comprises one or more different mammalian cell strains.

10. The method of claim 1, wherein the cell population comprises one or more different insect cell strains.

11. The method of claim 1, wherein the growth medium is selected from the group consisting of a liquid medium and a solid medium.

12. The method of claim 11, wherein the solid medium comprises a hydrogel.

13. The method of claim 11, wherein the solid medium comprises at least one gel-based material.

14. The method of claim 1, further comprising maintaining the cell population in a chamber, and flowing the growth medium through the chamber.

15. The method of claim 14, further comprising measuring the electrical parameter in different portions of the flowing growth medium as a function of time.

16. The method of claim 1, wherein the control gene is activated by at least one mechanism selected from the group consisting of: an external inducer; a self-activated inducer; and a combination of an external inducer and a self-activated inducer.

17. The method of claim 16, wherein the external inducer is selected from the group consisting of: exposure to optical radiation, a change in temperature, a chemical reagent, a viral agent, and combinations thereof.

18. The method of claim 1, wherein measuring the electrical parameter comprises measuring at least member selected from the group consisting of: a cyclic voltammetry signal for the growth medium; a potentiometry signal for the growth medium; an electrical conductivity of the growth medium; a phase difference between electrical signals measured for the growth medium; and combinations thereof.

19. The method of claim 1, wherein the electrical signal is an alternating current (AC) electrical signal.

20. The method of claim 1, wherein the electrical signal is a direct current (DC) electrical signal.

21. The method of claim 1, wherein the control gene is a single-gene lysis gene, a multi-gene lysis gene, one or more TA module genes, one or more toxin genes, or one or more peptide toxin gene.

22. The method of claim 1, wherein the control gene is activated by a target analyte.

23. The method of claim 22, wherein the target analyte comprises a chemical species.

24. The method of claim 22, wherein the target analyte comprises a biochemical molecule.

25. The method of claim 23 or claim 24, further comprising determining a relative concentration of the target analyte in the growth medium as a function of time based on the information about the cell population.

26. The method of claim 1, wherein the information about the cell population comprises information about a relative concentration of at least one metabolite generated by the cell population.

27. The method of claim 1, comprising measuring the electrical parameter of the growth medium without introducing a redox active species into the growth medium.

28. A system for monitoring a cell population, the apparatus comprising: a reservoir configured to contain a cell population, wherein the cell population comprises a cell strain comprising a control gene and a promoter sequence;electrodes configured to contact a growth medium in the reservoir;an electrical source connected to the electrodes and configured to apply an electrical signal to the growth medium;a detector configured to measure an electrical parameter of the growth medium as a function of time; andan electronic processor connected to the detector and configured to receive measurements of the electrical parameter, and to determine information about the cell population based on the measured electrical parameter.

29. The system of claim 28, wherein the reservoir is formed in a microfluidic device.

30. The system of claim 29, wherein the reservoir comprises an inlet and an outlet, and wherein the apparatus comprises a fluidic device configured to transport the growth medium through the reservoir from the inlet to the outlet.

31. The system of claim 28, wherein the reservoir comprises a recess configured to support a solid growth medium.

32. The system of claim 28, wherein the electrical parameter comprises an electrical admittance of the growth medium.

33. The system of claim 28, wherein the electrical parameter comprises an electrical impedance of the growth medium.

34. The system of claim 28, wherein the electrical parameter comprises a conductance of the growth medium.

35. The system of claim 28, wherein the electrical parameter comprises a resistance of the growth medium.

36. The system of claim 28, wherein applying the electrical signal comprises applying an electrical potential difference between the two electrodes.

37. The system of claim 28, wherein the cell population comprises one or more different bacterial strains.

38. The system of claim 28, wherein the cell population comprises one or more different yeast strains.

39. The system of claim 28, wherein the cell population comprises one or more different mammalian cell strains.

40. The system of claim 28, wherein the cell population comprises one or more different insect cell strains.

41. The system of claim 28, wherein the growth medium is selected from the group consisting of a liquid medium and a solid medium.

42. The system of claim 41, wherein the solid medium comprises a hydrogel.

43. The system of claim 41, wherein the solid medium comprises at least one gel-based material.

44. The system of claim 28, further comprising maintaining the cell population in a chamber, and flowing the growth medium through the chamber.

45. The system of claim 44, further comprising measuring the electrical parameter in different portions of the flowing growth medium as a function of time.

46. The system of claim 28, wherein the control gene is activated by at least one mechanism selected from the group consisting of: an external inducer; a self-activated inducer; and a combination of an external inducer and a self-activated inducer.

47. The system of claim 46, wherein the external inducer is selected from the group consisting of: exposure to optical radiation, a change in temperature, a chemical reagent, a viral agent, and combinations thereof.

48. The system of claim 28, wherein measuring the electrical parameter comprises measuring at least member selected from the group consisting of: a cyclic voltammetry signal for the growth medium; a potentiometry signal for the growth medium; an electrical conductivity of the growth medium; a phase difference between electrical signals measured for the growth medium; and combinations thereof.

49. The system of claim 28, wherein the electrical signal is an alternating current (AC) electrical signal.

50. The system of claim 28, wherein the electrical signal is a direct current (DC) electrical signal.

51. The system of claim 28, wherein the control gene is a single-gene lysis gene, a multi-gene lysis gene, one or more TA module genes, one or more toxin genes, or one or more peptide toxin gene.

52. The system of claim 28, wherein the control gene is activated by a target analyte.

53. The system of claim 52, wherein the target analyte comprises a chemical species.

54. The system of claim 52, wherein the target analyte comprises a biochemical molecule.

55. The system of claim 53 or claim 54, further comprising determining a relative concentration of the target analyte in the growth medium as a function of time based on the information about the cell population.

56. The system of claim 28, wherein the information about the cell population comprises information about a relative concentration of at least one metabolite generated by the cell population.

57. The system of claim 28, comprising measuring the electrical parameter of the growth medium without introducing a redox active species into the growth medium.

58. A method for determining a presence of a target analyte in a medium, the method comprising: culturing a cell population a medium, wherein: the cell population comprises a cell strain comprising a control gene and a promoter sequence;the promoter sequence is configured to bind a target analyte and, upon binding the target analyte, to activate the control gene to be expressed; andthe control gene is configured to modulate growth of the cell population;introducing the target analyte into the medium;measuring a change in an electrical parameter of the medium arising from a change in a concentration of a metabolite generated by the cell population following introduction of the target analyte; andidentifying a presence of the target analyte in the medium based on the measured change in the electrical parameter.

59. The method of claim 58, wherein the target analyte is a protein, oligonucleotide, or chemical compound.

60. The method of claim 59, wherein the chemical compound is a metal-containing chemical compound.

61. The method of claim 58, wherein the electrical parameter comprises an electrical admittance of the growth medium.

62. The method of claim 58, wherein the electrical parameter comprises an electrical impedance of the growth medium.

63. The method of claim 58, wherein the electrical parameter comprises a conductance of the growth medium.

64. The method of claim 58, wherein the electrical parameter comprises a resistance of the growth medium.

65. The method of claim 58, wherein applying the electrical signal comprises applying an electrical potential difference between the two electrodes.

66. The method of claim 58, wherein the cell population comprises one or more different bacterial strains.

67. The method of claim 58, wherein the cell population comprises one or more different yeast strains.

68. The method of claim 58, wherein the cell population comprises one or more different mammalian cell strains.

69. The method of claim 58, wherein the cell population comprises one or more different insect cell strains.

70. The method of claim 58, wherein the growth medium is selected from the group consisting of a liquid medium and a solid medium.

71. The method of claim 70, wherein the solid medium comprises a hydrogel.

72. The method of claim 70, wherein the solid medium comprises at least one gel-based material.

73. The method of claim 58, further comprising maintaining the cell population in a chamber, and flowing the growth medium through the chamber.

74. The method of claim 73, further comprising measuring the electrical parameter in different portions of the flowing growth medium as a function of time.

75. The method of claim 58, wherein the control gene is activated by at least one mechanism selected from the group consisting of: an external inducer; a self-activated inducer; and a combination of an external inducer and a self-activated inducer.

76. The method of claim 75, wherein the external inducer is selected from the group consisting of: exposure to optical radiation, a change in temperature, a chemical reagent, a viral agent, and combinations thereof.

77. The method of claim 58, wherein measuring the electrical parameter comprises measuring at least member selected from the group consisting of: a cyclic voltammetry signal for the growth medium; a potentiometry signal for the growth medium; an electrical conductivity of the growth medium; a phase difference between electrical signals measured for the growth medium; and combinations thereof.

78. The method of claim 58, wherein the electrical signal is an alternating current (AC) electrical signal.

79. The method of claim 58, wherein the electrical signal is a direct current (DC) electrical signal.

80. The method of claim 58, wherein the control gene is a single-gene lysis gene, a multi-gene lysis gene, one or more TA module genes, one or more toxin genes, or one or more peptide toxin gene.

81. The method of claim 58, wherein the control gene is activated by a target analyte.

82. The method of claim 81, wherein the target analyte comprises a chemical species.

83. The method of claim 81, wherein the target analyte comprises a biochemical molecule.

84. The method of claim 82 or claim 83, further comprising determining a relative concentration of the target analyte in the growth medium as a function of time based on the information about the cell population.

85. The method of claim 58, wherein the information about the cell population comprises information about a relative concentration of at least one metabolite generated by the cell population.

86. The method of claim 58, comprising measuring the electrical parameter of the growth medium without introducing a redox active species into the growth medium.

87. A device for detecting a target analyte, the device comprising: a substrate comprising a reservoir configured to contain a cell population, wherein: the cell population comprises a cell strain comprising a control gene and a promoter sequence;the promoter sequence is configured to bind a target analyte and, upon binding the target analyte, to activate the control gene to be expressed; andthe control gene is configured to modulate growth of the cell population;an inlet formed on or in the substrate and connected to the reservoir;a fluid delivery mechanism connected to the inlet and configured to introduce the target analyte into the reservoir;electrodes configured to contact a medium supporting the cell population in the reservoir;an electrical source connected to the electrodes and configured to apply an electrical signal to the medium;a detector configured to measure an electrical parameter of the medium arising from a change in a concentration of a metabolite generated by the cell population following introduction of the target analyte; andan electronic processor connected to the detector and configured to receive measurements of the electrical parameter, and to identify the target analyte based on the measured change in the electrical parameter.

88. The device of claim 87, wherein the electrical parameter comprises an electrical admittance of the growth medium.

89. The device of claim 87, wherein the electrical parameter comprises an electrical impedance of the growth medium.

90. The device of claim 87, wherein the electrical parameter comprises a conductance of the growth medium.

91. The device of claim 87, wherein the electrical parameter comprises a resistance of the growth medium.

92. The device of claim 87, wherein applying the electrical signal comprises applying an electrical potential difference between the two electrodes.

93. The device of claim 87, wherein the cell population comprises one or more different bacterial strains.

94. The device of claim 87, wherein the cell population comprises one or more different yeast strains.

95. The device of claim 87, wherein the cell population comprises one or more different mammalian cell strains.

96. The device of claim 87, wherein the cell population comprises one or more different insect cell strains.

97. The device of claim 87, wherein the growth medium is selected from the group consisting of a liquid medium and a solid medium.

98. The device of claim 97, wherein the solid medium comprises a hydrogel.

99. The device of claim 97, wherein the solid medium comprises at least one gel-based material.

100. The device of claim 87, further comprising maintaining the cell population in a chamber, and flowing the growth medium through the chamber.

101. The device of claim 100, further comprising measuring the electrical parameter in different portions of the flowing growth medium as a function of time.

102. The device of claim 87, wherein the control gene is activated by at least one mechanism selected from the group consisting of: an external inducer; a self-activated inducer; and a combination of an external inducer and a self-activated inducer.

103. The device of claim 102, wherein the external inducer is selected from the group consisting of: exposure to optical radiation, a change in temperature, a chemical reagent, a viral agent, and combinations thereof.

104. The device of claim 87, wherein measuring the electrical parameter comprises measuring at least member selected from the group consisting of: a cyclic voltammetry signal for the growth medium; a potentiometry signal for the growth medium; an electrical conductivity of the growth medium; a phase difference between electrical signals measured for the growth medium; and combinations thereof.

105. The device of claim 87, wherein the electrical signal is an alternating current (AC) electrical signal.

106. The device of claim 87, wherein the electrical signal is a direct current (DC) electrical signal.

107. The device of claim 87, wherein the control gene is a single-gene lysis gene, a multi-gene lysis gene, one or more TA module genes, one or more toxin genes, or one or more peptide toxin gene.

108. The device of claim 87, wherein the control gene is activated by a target analyte.

109. The device of claim 108, wherein the target analyte comprises a chemical species.

110. The device of claim 108, wherein the target analyte comprises a biochemical molecule.

111. The device of claim 109 or claim 110, further comprising determining a relative concentration of the target analyte in the growth medium as a function of time based on the information about the cell population.

112. The device of claim 87, wherein the information about the cell population comprises information about a relative concentration of at least one metabolite generated by the cell population.

113. The device of claim 87, comprising measuring the electrical parameter of the growth medium without introducing a redox active species into the growth medium.

114. The device of claim 87, wherein the reservoir is formed in a microfluidic device.

115. The device of claim 114, wherein the reservoir comprises an inlet and an outlet, and wherein the device comprises a fluidic device configured to transport the growth medium through the reservoir from the inlet to the outlet.

116. The device of claim 87, wherein the reservoir comprises a recess configured to support a solid growth medium.