Methods to identify modulators of actin-binding proteins
The present disclosure provides methods for identifying compounds that cause structural changes in a protein bound to an actin filament. The methods include the use of cells that include two actin-binding proteins, each labeled with a chromophore, and exposing the cells to a test compound. The method further includes detecting a change in fluorescence resonance energy transfer (FRET) between the chromophores.
1. A method for identifying a compound that alters fluorescence resonance energy transfer (FRET) of a protein comprising:
providing a genetically engineered cell comprising a first protein and a second protein,
wherein the first protein comprises a first heterologous domain that comprises a first probe, and the first protein comprises either a CH domain-containing actin-binding domain or a tandem-CH, actin-binding domain,
wherein the second protein comprises a second heterologous domain that comprises a second probe;
wherein each protein binds to an actin filament in the cell in a spatial proximity to result in detectable FRET between the first and second probes;
contacting the cell with a test compound to form a mixture; and
measuring the fluorescence lifetime of the first probe, the second probe, or the combination thereof.
2. The method of claim 1 , wherein a difference between the fluorescence lifetime in the presence of the test compound and the fluorescence lifetime in the absence of the test compound indicates that the test compound alters the FRET of the target protein.
3. The method of claim 1 wherein the second protein is a fusion protein comprising a Lifeact protein and a red fluorescent protein.
4. The method of claim 1 wherein the Förster distance between the first probe and the second probe is at least 52 angstroms (Å).
5. The method of claim 1 wherein the first heterologous domain is located at the amino-terminal end of the first protein.
6. The method of claim 1 wherein the first heterologous domain is located at the carboxy-terminal end of the first protein.
7. The method of claim 1 wherein the first probe is a donor probe and the second probe is an acceptor probe.
8. The method of claim 1 wherein the measuring comprises capturing fluorescence lifetime waveforms emitted by the donor probe or the acceptor probe.
9. The method of claim 1 wherein the fluorescence lifetime of the donor probe is changed in the presence of the test compound.
10. The method of claim 9 wherein the fluorescence lifetime of the donor probe is reduced in the presence of the test compound.
11. The method of claim 1 wherein the fluorescence lifetime of the donor probe is unchanged in the presence of the test compound.
12. The method of claim 1 wherein the cell is exposed to an excitation light for no greater than 5 seconds.
13. The method of claim 1 wherein the first protein comprises a wild-type protein that further comprises the first heterologous domain.
14. The method of claim 1 wherein the first protein is a mutant actin-binding protein comprising a wild-type protein and at least one mutation.
15. The method of claim 1 wherein the at least one mutation is present in the tandem-CH, actin-binding domain or in the CH domain-containing actin-binding domain.
16. The method of claim 14 wherein the mutant actin-binding protein binds the actin filament with an affinity that is greater than the first protein in the absence of the at least one mutation.
17. The method of claim 1 wherein the first protein comprises a β-III-spectrin, the β-III-spectrin comprising a mutation that correlates with a disease in a human.
18. The method of claim 17 wherein the disease is spinocerebellar ataxia type 5.
19. The method of claim 17 wherein the mutation is L253P.
20. The method of claim 1 further comprising performing a counter screen, wherein the counter screen comprises:
providing a genetically engineered cell comprising the first protein and the second probe;
contacting the cell with the test compound to form a mixture; and
measuring the fluorescence lifetime of the first probe, the second probe, or the combination thereof.