Labeled substrate conjugates for identifying enzyme inhibitors
View Patent ↗This invention provides labeled-substrate conjugates for assaying enzymes, particularly neuraminidases. Also provided are assays that are useful for identifying compounds that inhibit sialyltransferases or neuraminidases and may be useful in treating subjects with influenza. In particular, the present invention relates to methods of using such labeled substrate conjugates to screen for enzyme inhibitors, particularly in a high-throughput format.
1. An assay complex comprising at least one test ligand and at least one composition comprising a solid support and a conjugate comprising a detectable label covalently attached to the substrate of a neuraminidase wherein modification of said substrate causes a detectable change in said label, wherein the test ligand is attached by covalent interaction with said solid support.
2. The complex of claim 1 , wherein said detectable label is selected from the group consisting of a fluorogenic label and a chromogenic label.
3. The complex of claim 2 , wherein said fluorogenic label is selected from the group consisting of 2′-(4-methylumbelliferyl)-α-D-acetyl-neuraminic acid and fluoroscein.
4. The complex of claim 1 , wherein the substrate is sialic acid.
5. The complex of claim 1 wherein the conjugate has the formula selected from the group consisting of compounds 10, 15 and 25.
6. The complex of claim 1 , wherein said at least one test ligand is a library of test ligands.
7. The complex of claim 1 , wherein said substrate is sialic acid.
8. The complex of claim 1 , wherein the conjugate is attached by covalent interaction with the solid support.
9. The complex of claim 1 , wherein the conjugate is attached by noncovalent interaction with the solid support.
10. The complex of claim 1 , wherein the solid support is selected from the group consisting of a bead, a slide and a chip.
11. The complex of claim 1 , wherein the solid support is a bead.
12. The complex of claim 7 wherein the conjugate has the formula selected from the group consisting of compounds 10, 15 and 25.
13. An assay complex comprising at least one test ligand attached to a solid support and at least one detectable label-substrate conjugate comprising a detectable label covalently attached to a first substrate of an enzyme and a quencher attached to a second substrate of said enzyme wherein modification of said substrates causes a detectable change in said label and either said detectable label covalently attached to a first substrate of said enzyme or said quencher attached to a second substrate of an enzyme is attached to said solid support.
14. The complex of claim 13 , wherein said at least one test ligand is a library of test ligands.
15. The complex of claim 13 wherein the detectable label covalently attached to a first substrate of an enzyme has the formula selected from the group consisting of compounds 55, 59 and 60.
16. The complex of claim 13 wherein the quencher attached to a second substrate of an enzyme having the formula selected from the group consisting of compounds 64, 69, and 73.
17. The complex of claim 13 , wherein the conjugate is attached by covalent interaction with the solid support.
18. The complex of claim 13 , wherein the conjugate is attached by noncovalent interaction with the solid support.
19. The complex of claim 13 , wherein the solid support is selected from the group consisting of a bead, a slide and a chip.
20. The complex of claim 13 , wherein the solid support is a bead.
21. A method of identifying an enzyme inhibitor comprising:
a) combining in an assay mixture the complex of claim 1 and a sufficient quantity of said enzyme to react with the substrate under noninhibitory conditions; and
b) detecting a change in said label in said assay mixture upon combination with said enzyme; wherein the presence of an enzyme inhibitor prevents said enzyme from modifying said substrate and causing a change in said detectable label; and
c) identifying the test ligand which prevents said detectable change.
22. The method of claim 21 , wherein the enzyme is neuraminidase or sialyltransferase and the natural substrate is sialic acid.
23. The method of claim 21 , wherein said change is a fluorescent emission.
24. The method of claim 23 , wherein the detecting step is performed by monitoring the change in fluorescence emission of fluorescein attached to sialic acid.
25. The method of claim 23 , wherein the detecting step is performed by monitoring the change in fluorescence emission of 2′-(4-methylumberllifreyl)-α-D-acetyl-neuraminic acid attached to sialic acid.