High-throughput, high-precision methods for detecting protein structural changes in living cells
Methods for identifying a compound that alters fluorescence resonance energy transfer (FRET) of a protein. The methods include use of a genetically engineered cell that includes a target protein. The target protein includes one or more heterologous domains. In one embodiment, a target protein includes two heterologous domains, and in another embodiment, the target protein includes a heterologous domain and the cell further includes a second protein that includes a heterologous domain. A heterologous domain may include a chromophore or an amino acid to which a fluorescent dye attaches. The fluorescence lifetime of one or more chromophore, one or more fluorescent dye, or the combination thereof, is measured after contacting the cell with a compound 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.
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 target protein,
wherein the cell is a live cell,
wherein the target protein comprises two heterologous domains, wherein a first heterologous domain comprises a first chromophore, wherein a second heterologous domain comprises a second chromophore, and wherein each heterologous domain comprises a fluorescent protein;
contacting the live cell with a test compound to form a mixture;
measuring the fluorescence lifetime of the first chromophore, the second chromophore, or the combination thereof, of the live cell,
wherein the measuring comprises use of a plate reader and direct waveform recording of fluorescence lifetime decays,
wherein the measuring occurs over a period of time no greater than 0.5 seconds;
calculating a coefficient of variation (CV) for the fluorescence lifetime of the first chromophore, the second chromophore, or the combination thereof, wherein CV is no greater than 0.5%; and
calculating a Z′ parameter, wherein the Z′ parameter is >0.5;
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.
2. The method of claim 1 wherein the fluorescence lifetime of the first chromophore, the second chromophore, or the combination thereof, is changed in the presence of the test compound.
3. The method of claim 1 adapted for use in a high-throughput format.
4. The method of claim 1 wherein the target protein is stably expressed by the genetically engineered cell.
5. The method of claim 1 wherein the cell is a eukaryotic cell.
6. The method of claim 5 wherein the cell is a vertebrate cell.
7. The method of claim 1 wherein the measuring occurs over a period of time no greater than 0.001 seconds.
8. The method of claim 1 wherein the first chromophore and the second chromophore are selected from a green fluorescent protein, a red fluorescent protein, and a yellow fluorescent protein, or an analogue thereof.
9. The method of claim 1 wherein the cell is in suspension.
10. A method for identifying a compound that alters fluorescence resonance energy transfer (FRET) of a protein comprising:
providing a genetically engineered cell comprising a target protein and a second protein,
wherein the cell is a live cell,
wherein the target protein comprises a first heterologous domain that comprises a first chromophore, and wherein the second protein comprises a second heterologous domain that comprises a second chromophore, and wherein each heterologous domain comprises a fluorescent protein;
contacting the live cell with a test compound to form a mixture; and
measuring the fluorescence lifetime of energy emitted by the first chromophore, the second chromophore, or the combination thereof, of the live cell,
wherein the measuring comprises use of a plate reader and direct waveform recording of fluorescence lifetime decays,
wherein the measuring occurs over a period of time no greater than 0.5 seconds;
calculating a coefficient of variation (CV) for the fluorescence lifetime of the first chromophore, the second chromophore, or the combination thereof, wherein the CV is no greater than 0.5%; and
calculating a Z′ parameter, wherein the Z′ parameter is >0.5;
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, the second protein, or the combination thereof.
11. The method of claim 10 wherein the target protein and second protein are stably expressed by the genetically engineered cell.
12. The method of claim 10 wherein the fluorescence lifetime of the first chromophore, the second chromophore, or the combination thereof, is changed in the presence of the test compound.
13. The method of claim 10 adapted for use in a high-throughput format.
14. The method of claim 10 wherein the cell is a eukaryotic cell.
15. The method of claim 14 wherein the cell is a vertebrate cell.
16. The method of claim 10 wherein the measuring occurs over a period of time no greater than 0.001 seconds.
17. The method of claim 10 wherein the first chromophore and the second chromophore are selected from a green fluorescent protein, a red fluorescent protein, and a yellow fluorescent protein, or an analogue thereof.
18. The method of claim 10 wherein the cell is in suspension.
19. The method of claim 1 wherein the target protein is transiently expressed by the genetically engineered cell.