MRI probes of membrane potential
View Patent ↗The invention provides methods and compositions for molecular resonance imaging of membrane potential. The compositions comprise an indicator moiety attached through an optional linker to a macrocycle component that binds a lanthanide. The indicator moiety changes conformation in response to alterations in membrane potential and alters the interaction of the bound lanthanide with water. This alteration produces a detectable change in MRI signal , notably the T 1 value. A preferred indicator moiety is spiropyran as it exhibits membrane-potential driven interconversions between the closed-ring spiropyran conformer and the extended merocyanine conformer. A preferred macrocycle is DO3A, known to bind gadolinium and an established MRI contrast agent. The methods of the invention comprise in vivo and in vitro uses of compositions of the invention to obtain MRI images that provide information about membrane potential.
1. A compound, comprising:
an indicator moiety capable of adopting at least two conformations, wherein the equilibrium between said at least two conformations is altered by a membrane potential, wherein said indicator moiety is selected from the group consisting of a spiropyran, a merocyanine, a cyanine, and an indoline;
a DO3A bound to said indicator moiety;
and a lanthanide chelated within said DO3A, wherein the interaction of said chelated lanthanide with a solvent is altered by a change in the equilibrium between said at least two conformers of said indicator moiety.
2. The compound of claim 1 , wherein said solvent is water.
3. The compound of claim 1 , wherein said DO3A is bound to said indicator moiety through a linker.
4. The compound of claim 1 , wherein said indicator moiety is a spiropyran.
5. The compound of claim 4 , wherein said spiropyran is spirobenzopyran.
6. The compound of claim 4 , wherein said spiropyran is spirobenzothiopyran.
7. The compound of claim 1 , wherein said lanthanide is gadolinium.
8. The compound of claim 1 , comprising the formula:
wherein R 1 is selected from the group consisting of C n H 2n+2 , C n H 2n , and a combination of both and wherein n is 0 to 4, inclusive;
wherein each of R 2 –R 7 is independently selected from the group consisting of H, CH 3, phenyl, and a bulky steric-hindering group;
and wherein A − is independently selected from COO − , PO 3 2− , and another lanthanide—coordinating group.
9. The compound of claim 8 , wherein R 1 is CH 2 , R 2 –R 7 each is H, and A − is COO − .
10. The compound of claim 8 , wherein said La is Gd.
11. A composition, comprising the compound of claim 1 and a pharmaceutically acceptable excipient.
12. A composition, comprising the compound of claim 4 and a pharmaceutically acceptable excipient.
13. A composition, comprising the compound of claim 7 and a pharmaceutically acceptable excipient.
14. A composition, comprising the compound of claim 8 and a pharmaceutically acceptable excipient.
15. A composition, comprising the compound of claim 9 and a pharmaceutically acceptable excipient.
16. A composition, comprising the compound of claim 10 and a pharmaceutically acceptable excipient.
17. A method of generating a magnetic resonance image of a membrane potential, comprising:
contacting a cell with the compound of claim 1 ; and
generating a magnetic resonance image of said cell, wherein said magnetic resonance image provides information about the membrane potential of said cell.
18. A method of generating a magnetic resonance image of a membrane potential, comprising:
contacting a cell with a compound of claim 8 ; and
generating a magnetic resonance image of said cell, wherein said magnetic resonance image provides information about the membrane potential of said cell.
19. A method of testing a compound for suitability as a magnetic resonance imaging probe of membrane potential, comprising:
contacting an electrically-excitable cultured cell with a compound of claim 1 ;
generating a magnetic resonance image of said cell; and
determining whether said magnetic resonance image provides information about the membrane potential of said electrically excitable cell.
20. The method of claim 19 , wherein said electrically excitable cell is selected from the group consisting of a neuron and a muscle.
21. The method of claim 19 , wherein said electrically excitable cell is a cardiac muscle cell.
22. The method of claim 19 , wherein said culture is a three-dimensional culture.
23. A method of testing a compound for suitability as a magnetic resonance imaging probe of membrane potential, comprising:
contacting an electrically-excitable cultured cell with a compound of claim 8 ;
generating a magnetic resonance image of said cell; and
determining whether said magnetic resonance image provides information about the membrane potential of said electrically excitable cell.
24. The method of claim 23 , wherein said electrically excitable cell is selected from the group consisting of a neuron and a muscle.
25. The method of claim 23 , wherein said electrically excitable cell is a cardiac muscle cell.
26. The method of claim 23 , wherein said culture is a three-dimensional culture.
27. The compound of claim 8 wherein R 1 is CH 2 , R 2 –R 7 each is H, A− is PO 3 2− , and La is Gd.