Fluorescence polarization method for determining viral inhibitors
Methods for determining inhibitors of protein interactions are provided. The method involves evaluation of potential inhibitors that can inhibit or prevent protein interactions. The method provides for high-throughput identification of novel therapeutics that can treat a disease or disorder by inhibiting protein interactions.
1. A method for determining inhibitors of subunit interaction comprising:
providing a test sample comprising at least a first viral polymerase subunit or fragment thereof and at least a second viral polymerase subunit or fragment thereof, the first subunit or fragment thereof and the second subunit or fragment thereof which interacts together and the first or second subunit or fragment thereof comprising a fluorescent label;
measuring fluorescence polarization of the test sample;
combining at least one test compound and the test sample to form a test mixture;
measuring fluorescence polarization of the test mixture; and
comparing fluorescence polarization of the test mixture with fluorescence polarization of the test sample to determine if the at least one test compound has inhibits subunit interaction.
2. The method of claim 1 in which the first viral polymerase subunit or fragment thereof includes a peptide having SEQ ID No.: 1.
3. The method of claim 1 in which the second viral polymerase subunit or fragment thereof includes a peptide having SEQ ID No.:2.
4. The method of claim 1 wherein the at least one test compound includes a plurality of test compounds.
5. The method of claim 1 in which the fluorescent label comprises pentafluorescein-derivative Oregon Green 514.
6. The method of claim 1 in which the at least one test compound is a member of a combinatorial library.
7. The method of claim 6 in which remaining members of the library are sequentially tested in a plurality of test mixtures.
8. A method of testing compounds for inhibiting herpes simplex virus DNA polymerase, the method comprising:
providing a test sample comprising a peptide which is substantially homologous to an eighteen amino acid C-terminal fragment of catalytic unit of herpes simplex virus DNA polymerase and a functional fragment of processivity subunit of herpes simplex virus DNA polymerase, the C-terminal fragment of catalytic unit of herpes simplex virus DNA polymerase comprising a fluorescent label;
measuring fluorescence polarization of the test sample;
combining at least one test compound and test sample to form a test mixture; and
measuring fluorescence polarization of the test mixture; and
comparing fluorescence polarization of the test mixture to fluorescence polarization of the test sample to determine level of inhibition of the herpes simplex virus DNA polymerase by the test compound.
9. The method of claim 8 in which a decrease in fluorescence polarization of test mixture, when compared to fluorescence polarization of test sample, can be correlated to a decrease in DNA synthesis by herpes simplex virus DNA polymerase.
10. The method of claim 9 in which the C-terminal fragment comprises a peptide including SEQ ID NO.:1.
11. The method of claim 9 in which the functional fragment of the processivity subunit comprises a protein including SEQ ID NO.: 2.
12. The method of claim 9 in which the C-terminal fragment comprises a peptide including SEQ ID NO.:1 and the functional fragment of the processivity subunit comprising a protein including SEQ ID NO.: 2.
13. The method of claim 1 , wherein the test compound comprises the formula
or pharmaceutically suitable salt or solvate thereof, wherein X 1 is
and X 2 is
wherein each of R 1 and R 2 is a member selected from the group consisting of: —NO 2 , —NH 2 , —OH, —COOH, —Cl, —Br, —I, and —O—X, wherein X is a saturated or unsaturated hydrocarbon including 1–8 carbon atoms.
14. The method of claim 1 , wherein the test compound comprises the formula
or a pharmaceutically suitable salt or solvate thereof, wherein X 1 is
and X 2 is
wherein each of R 1 and R 2 is a member selected from the group consisting of: —NO 2 , —NH 2 , —OH, —COOH, —Cl, —Br, —I, and —O—X, wherein X is a saturated or unsaturated hydrocarbon including 1–8 carbon atoms.