Drug targets for the treatment of neurodegenerative disorders

1. A method of identifying an agent for diminishing cellular toxicity associated with an α-synuclein polypeptide of Parkinson's Disease, comprising:

contacting a first yeast cell with a candidate agent, wherein the first cell expresses an α-synuclein polypeptide and a wild-type YPK1 gene, and wherein expression of the α-synuclein polypeptide is toxic to the cell;

contacting a second yeast cell with the candidate agent, wherein the second cell expresses the α-synuclein polypeptide and does not express the wild-type YPK1 gene; and

determining for the first and second cells the level of a biological activity or characteristic associated with the toxicity of the α-synuclein polypeptide, wherein the biological activity or characteristic associated with the toxicity is selected from the group consisting of decreased cell viability relative to a cell that does not express the α-synuclein polypeptide and formation of inclusion bodies in the cell, whereby if the first cell (a) exhibits a decrease of the biological activity or characteristic relative to a control cell that has not been contacted with the candidate agent and (b) does not exhibit a decrease of the biological activity or characteristic relative to the second cell, the candidate agent is identified as an agent for diminishing the cellular toxicity associated with the α-synuclein polypeptide.

2. The method of claim 1 , wherein the second cell contains a null allele of the wild-type YPK1 gene.

3. The method of claim 1 , wherein the second cell has a deletion of the wild-type YPK1 gene.

4. The method of claim 1 , wherein the biological activity or characteristic associated with the toxicity of the α-synuclein polypeptide is decreased cell viability relative to a cell that does not express the α-synuclein polypeptide.

5. The method of claim 1 , wherein the biological activity or characteristic associated with the toxicity of the α-synuclein polypeptide is the formation of inclusion bodies in the cell.

6. The method of claim 1 , wherein the candidate agent is a small molecule, a nucleic acid, a proteinaceous agent, or a peptidomimetic.

7. The method of claim 1 , wherein the candidate agent is a synthetic compound.

8. The method of claim 1 , wherein the candidate agent is a natural compound.

9. The method of claim 1 , wherein the contacting the cell with the candidate agent comprises transformation or culturing the cell in media containing the candidate agent.

10. The method of claim 1 , wherein the α-synuclein polypeptide is a fusion protein.

11. The method of claim 10 , wherein the fusion protein comprises a reporter polypeptide.

12. The method of claim 10 , wherein the fusion protein comprises a myc epitope.

13. A method of identifying an agent for diminishing cellular toxicity associated with an α-synuclein polypeptide of Parkinson's Disease, comprising:

(1) contacting a sample comprising YPK1 protein with a candidate agent;

(2) determining the level of a biological activity associated with the YPK1 protein relative to a control sample comprising protein that has not been contacted with the candidate agent, wherein the biological activity is selected from the group consisting of kinase activity, sphingolipid signaling, and endocytosis; and

(3) if the sample comprising YPK1 protein exhibits a decrease in the biological activity relative to the control sample, then

(a) contacting a yeast cell expressing the YPK1 protein and an α-synuclein polypeptide with the candidate agent, wherein expression of the α- synuclein polypeptide is toxic to the cell; and

(b) determining for the yeast cell the level of a biological activity or characteristic associated with the toxicity of the α-synuclein polypeptide, said level relative to a control yeast cell that expresses the YPK1 protein and the α-synuclein polypeptide and that has not been contacted with the candidate agent, wherein the biological activity or characteristic associated with the toxicity is selected from the group consisting of decreased cell viability relative to a cell that does not express the a-synuclein polypeptide and formation of inclusion bodies in the cell,

whereby if the yeast cell exhibits a decrease in the biological activity or characteristic relative to the control cell, the candidate agent is identified as an agent for diminishing the cellular toxicity associated with the α-synuclein polypeptide.

14. The method of claim 13 , further comprising contacting a second yeast cell with the candidate agent, wherein the second cell expresses the α-synuclein polypeptide and does not express the YPK1 protein; and

determining for the second yeast cell the level of the biological activity or characteristic associated with the expression of the α-synuclein polypeptide, whereby if the first yeast cell exhibits a decrease of the biological activity or characteristic relative to the control yeast cell and does not exhibit a decrease of the biological activity or characteristic relative to the second yeast cell, the agent is identified as an agent for diminishing the cellular toxicity associated with the α-synuclein polypeptide.

15. The method of claim 13 , wherein the biological activity or characteristic associated with the toxicity of the α-synuclein polypeptide is decreased cell viability relative to a cell that does not express the α-synuclein polypeptide.

16. The method of claim 13 , wherein the biological activity or characteristic associated with the toxicity of the α-synuclein polypeptide is the formation of inclusion bodies in the cell.

17. The method of claim 13 , wherein the candidate agent is a small molecule, a nucleic acid, a proteinaceous agent, or a peptidomimetic.

18. The method of claim 13 , wherein the candidate agent is a synthetic compound.

19. The method of claim 13 , wherein the candidate agent is a natural compound.

20. The method of claim 13 , wherein the contacting the cell with the candidate agent comprises transformation or culturing the cell in media containing the candidate agent.