Fluorescent protein voltage sensors for measuring membrane potential and imaging high-frequency neuronal electrical activity
Fluorescent protein voltage sensors for measuring membrane potential and imaging high-frequency neuronal electrical activity are disclosed. In particular, the invention relates to engineered protein voltage sensors that comprise a voltage-sensing domain comprising four transmembrane domains linked to a circularly permuted fluorescent protein, which is inserted into the extracellular loop between the third (S3) and fourth (S4) transmembrane segments of the voltage-sensing domain. Such fluorescent protein voltage sensors can be used for measuring the electrical activity of neurons, including single action potentials, trains of action potentials, and subthreshold potential changes and, in particular, for imaging high-frequency neuronal electrical activity. Additionally, fluorescent protein voltage sensors can be used for a variety of other purposes, including measuring the membrane potential of any cell, including other excitable cells such as cardiac cells and endocrine cells, and for screening agents that target ion channels for their effects on membrane potential.
1. A polynucleotide encoding a fluorescent protein voltage sensor comprising: (i) a voltage-sensing domain (VSD) comprising four transmembrane segments; and (ii) a circularly permuted fluorescent protein, wherein the circularly permuted fluorescent protein is inserted into an extracellular loop between the third transmembrane segment (S3) and the fourth transmembrane segment (S4) of the VSD at a position 4, 5, or 6 amino acids downstream of the C-terminal end of the S3.
2. A recombinant polynucleotide comprising the polynucleotide of claim 1 operably linked to a promoter.
3. The recombinant polynucleotide of claim 2 , wherein the promoter is a cell-type specific promoter.
4. The recombinant polynucleotide of claim 3 , wherein the cell-type specific promoter is a neuron-specific promoter or a cardiac-specific promoter.
5. The recombinant polynucleotide of claim 2 comprising a polynucleotide selected from the group consisting of:
a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:12;
b) a polynucleotide comprising a nucleotide sequence at least 95% identical to the nucleotide sequence of SEQ ID NO:12, wherein the fluorescence intensity of the encoded polypeptide is voltage dependent;
c) a polynucleotide encoding a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOS:1-3 and SEQ ID NOS:13-17; and
d) a polynucleotide encoding a polypeptide comprising a sequence at least 95% identical to an amino acid sequence selected from the group consisting of SEQ ID NOS:1-3 and SEQ ID NOS:13-17, wherein the fluorescence intensity of the polypeptide is voltage dependent.
6. A host cell comprising the recombinant polynucleotide of claim 2 .
7. The host cell of claim 6 , wherein the host cell is an excitable cell.
8. The host cell of claim 7 , wherein the excitable cell is selected from the group consisting of a neuron, a cardiac cell, and an endocrine cell.
9. A method for monitoring the membrane potential of an excitable cell, the method comprising:
a) transfecting the excitable cell with the recombinant polynucleotide of claim 2 , whereby the fluorescent protein voltage sensor is expressed and localizes to a membrane of the cell; and
b) illuminating the excitable cell with light at an excitation wavelength of the fluorescent protein voltage sensor; and
c) monitoring the fluorescence response, wherein the intensity of the fluorescence emitted by the fluorescent protein voltage sensor is correlated with the membrane potential of the excitable cell.
10. The method of claim 9 , wherein the excitable cell is transfected in vitro or in vivo.
11. The method of claim 9 , wherein the membrane is a plasma membrane or an organelle membrane.
12. The method of claim 9 , wherein the fluorescence response is monitored after exposing the excitable cell to a stimulus.
13. The method of claim 12 , wherein the stimulus is selected from the group consisting of an electrical current, a drug, a ligand for a receptor, a ligand for an ion channel, a ligand for an ion transporter, a hormone, and a second messenger.
14. The method of claim 9 , wherein changes in the intensity of the fluorescence emitted by the fluorescent protein voltage sensor indicate depolarization.
15. The method of claim 9 , wherein monitoring the fluorescence response comprises performing fluorescence microscopy.
16. The method of claim 15 , wherein fluorescence microscopy is performed using confocal microscopy, two-photon excitation microscopy, light sheet microscopy, or light-field microscopy.
17. The method of claim 9 , wherein the excitable cell is selected from the group consisting of a neuron, a cardiac cell, and an endocrine cell.
18. The method of claim 17 , wherein the fluorescent protein voltage sensor localizes to the plasma membrane of a cell body, dendrite, or axon of the neuron or the sarcolemma of the cardiac cell.
19. The method of claim 9 , wherein monitoring the fluorescence response comprises detecting a single action potential.
20. The method of claim 9 , wherein monitoring the fluorescence response comprises detecting a subthreshold potential change.
21. The method of claim 20 , wherein the subthreshold potential change is an excitatory postsynaptic potential (EPSP) or an inhibitory postsynaptic potential (IPSP).
22. The method of claim 9 , wherein monitoring the fluorescence response comprises detecting depolarization or hyperpolarization.
23. The method of claim 9 , wherein monitoring the fluorescence response comprises detecting a train of action potentials.
24. The method of claim 23 , wherein the action potential waveform has a frequency of up to 200 Hz.
25. A method for monitoring the membrane potential of an excitable cell, the method comprising:
a) inserting the fluorescent protein voltage sensor encoded by the polynucleotide of claim 1 into a membrane of the excitable cell; and
b) illuminating the excitable cell with light at an excitation wavelength of the fluorescent protein voltage sensor; and
c) monitoring the fluorescence response, wherein the intensity of the fluorescence emitted by the fluorescent protein voltage sensor is correlated with the membrane potential of the excitable cell.
26. The method of claim 25 , wherein the membrane is a plasma membrane or an organelle membrane.
27. The method of claim 25 , wherein the fluorescence response is monitored after exposing the excitable cell to a stimulus.
28. The method of claim 27 , wherein the stimulus is selected from the group consisting of an electrical current, a drug, a ligand for a receptor, a ligand for an ion channel, a ligand for an ion transporter, a hormone, and a second messenger.
29. The method of claim 25 , wherein changes in the intensity of the fluorescence emitted by the fluorescent protein voltage sensor indicate depolarization.
30. The method of claim 25 , wherein monitoring the fluorescence response comprises performing fluorescence microscopy.
31. The method of claim 30 , wherein fluorescence microscopy is performed using confocal microscopy, two-photon excitation microscopy, light sheet microscopy, or light-field microscopy.
32. The method of claim 25 , wherein the excitable cell is selected from the group consisting of a neuron, a cardiac cell, and an endocrine cell.
33. The method of claim 32 , wherein the fluorescent protein voltage sensor localizes to the plasma membrane of a cell body, dendrite, axon of the neuron or the sarcolemma of the cardiac cell.
34. The method of claim 25 , wherein monitoring the fluorescence response comprises detecting a single action potential.
35. The method of claim 25 , wherein monitoring the fluorescence response comprises detecting a subthreshold potential change.
36. The method of claim 35 , wherein the subthreshold potential change is an excitatory postsynaptic potential (EPSP) or an inhibitory postsynaptic potential (IPSP).
37. The method of claim 25 , wherein monitoring the fluorescence response comprises detecting depolarization or hyperpolarization.
38. The method of claim 25 , wherein monitoring the fluorescence response comprises detecting a train of action potentials.
39. The method of claim 38 , wherein the action potential waveform has a frequency of up to 200 Hz.
40. A method of screening an agent for its effect on the membrane potential of an excitable cell, the method comprising:
a) monitoring the membrane potential of the excitable cell, according to the method of claim 9 , before and after treatment of the excitable cell with the agent; and
b) comparing the membrane potential before and after treatment of the cell with the agent to detect any changes in the membrane potential resulting from treatment of the excitable cell with the agent.
41. The method of claim 40 , wherein the agent is an ion channel modulator, an ion channel blocker, an ion channel opener, a ligand for an ion channel, a ligand for an ion transporter, a ligand for a receptor, a hormone, or a second messenger.
42. A method of screening an agent for its effect on the membrane potential of an excitable cell, the method comprising:
a) monitoring the membrane potential of the excitable cell, according to the method of claim 25 , before and after treatment of the excitable cell with the agent; and
b) comparing the membrane potential before and after treatment of the excitable cell with the agent to detect any changes in the membrane potential resulting from treatment of the excitable cell with the agent.
43. The method of claim 42 , wherein the agent is an ion channel modulator, an ion channel blocker, an ion channel opener, a ligand for an ion channel, a ligand for an ion transporter, a ligand for a receptor, a hormone, or a second messenger.
44. A method for producing a fluorescent protein voltage sensor, the method comprising:
a) transforming a host cell with the recombinant polynucleotide of claim 2 ;
b) culturing the transformed host cell under conditions whereby the fluorescent protein voltage sensor is expressed; and
c) isolating the fluorescent protein voltage sensor from the host cell.
45. A kit comprising the recombinant polynucleotide of claim 2 .
46. A kit comprising the host cell of claim 6 .
47. The polynucleotide of claim 1 , wherein the VSD is from a voltage sensitive phosphatase.
48. The polynucleotide of claim 1 , wherein the voltage sensitive phosphatase is from a bird, a fish, an amphibian, a reptile, or an insect.
49. The polynucleotide of claim 48 , wherein the voltage sensitive phosphatase is from Gallus gallus, Xenopus laevis, Danio rerio, Alligator mississippiensis , or Metaseiulus occidentalis.
50. The polynucleotide of claim 1 , wherein the VSD is from a voltage-gated ion channel or transporter.
51. The polynucleotide of claim 1 , wherein the VSD comprises a mutation comprising a substitution of a glutamine for the amino acid at the position corresponding to 153 numbered relative to the reference sequence of SEQ ID NO:4.
52. The polynucleotide of claim 1 , wherein the circularly permuted fluorescent protein emits green, blue, cyan, yellow, orange, red, or far-red light.
53. The polynucleotide of claim 1 , wherein the circularly permuted fluorescent protein is selected from the group consisting of circularly permuted green fluorescent protein (cpGFP), circularly permuted superfolder GFP (cpsfGFP), circularly permuted mApple (cpmApple), circularly permuted mCherry (cpmCherry), circularly permuted mKate (cpmKate), circularly permuted enhanced green fluorescent protein (cpEGFP), circularly permuted Venus (cpVenus), circularly permuted Citrine (cpCitrine), and circularly permuted enhanced yellow fluorescent protein (cpEYFP).
54. The polynucleotide of claim 53 , wherein the circularly permuted fluorescent protein is cpsfGFP or cpmApple.
55. The polynucleotide of claim 1 , wherein the polynucleotide is selected from the group consisting of:
a) a polynucleotide encoding a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOS:1-3 and SEQ ID NOS:13-17; and
b) a polynucleotide encoding a polypeptide comprising an amino acid sequence having at least 95% identity to an amino acid sequence selected from the group consisting of SEQ ID NOS:1-3 and SEQ ID NOS:13-17, wherein the fluorescence intensity of the polypeptide is voltage dependent.
56. The polynucleotide of claim 1 , wherein the VSD comprises a polypeptide selected from the group consisting of:
a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:4, SEQ ID NO:19, and SEQ ID NO:20; and
b) a polypeptide comprising an amino acid sequence having at least 95% identity to an amino acid sequence selected from the group consisting of SEQ ID NO:4, SEQ ID NO:19, and SEQ ID NO:20, wherein the polypeptide has voltage sensing characteristics.
57. The polynucleotide of claim 1 , wherein the circularly permuted fluorescent protein comprises a polypeptide selected from the group consisting of:
a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:5 and SEQ ID NO:18; and
b) a polypeptide comprising an amino acid sequence having at least 95% identity to an amino acid sequence selected from the group consisting of SEQ ID NO:5 and SEQ ID NO:18, wherein the fluorescence intensity of the fluorescent protein voltage sensor is voltage dependent.
58. The polynucleotide of claim 1 , wherein the fluorescent protein voltage sensor further comprises a targeting sequence.
59. The polynucleotide of claim 58 , wherein the targeting sequence is a membrane-targeting sequence or an organelle-targeting sequence.
60. The polynucleotide of claim 59 , wherein the membrane-targeting sequence is a prenylation sequence or a signal peptide.
61. The polynucleotide of claim 59 , wherein the targeting sequence localizes the fluorescent protein to a subcellular region of a cell.
62. The polynucleotide of claim 1 , wherein the circularly permuted fluorescent protein is inserted after the amino acid at the position corresponding to 147, 148, or 149 numbered relative to the reference sequence of SEQ ID NO:3.