Screening methods for the identification of agents that inhibit SIRT1 Tat deacetylase activity
View Patent ↗The present invention provides treatment methods involving modulating a sirtuin activity and/or a sirtuin mRNA and/or a sirtuin polypeptide level. In some embodiments, the present invention provides treatment methods involving modulating SIRT1 activity and/or SIRT mRNA and/or polypeptide level. The present invention provides methods of inhibiting SIRT1 Tat deacetylase activity. Methods of inhibiting SIRT1 Tat deacetylase activity are useful for treating immunodeficiency virus infections, particularly human immunodeficiency virus (HIV) infection. Thus, the present invention provides methods of treating an immunodeficiency virus infection, generally involving inhibiting SIRT1 Tat deacetylase activity. The present invention further provides methods of identifying agents that modulate sirtuin activity (e.g., SIRT1 activity), particularly ability of sirtuins to interact with (e.g., bind and/or deacetylate) a substrate, e.g., a viral substrate such as a Tat polypeptide. The present invention further provides active agents that modulate sirtuin activity or expression; and compositions, including pharmaceutical compositions, comprising the active agents.
1. An in vitro method of identifying an agent that inhibits SIRT1 Tat deacetylase activity, the method comprising:
contacting a cell that produces a SIRT1 Tat deacetylase polypeptide and an acetylated Tat polypeptide with a test agent; and
determining the level of acetylated Tat polypeptide in the cell compared to the level of acetylated Tat polypeptide in a control cell not contacted with the test agent, wherein a reduction in the level of acetylated Tat in the cell contacted with the test agent compared to the control cell indicates that the test agent inhibits SIRT1 Tat deacetylase activity.
2. The method of claim 1 , wherein the Tat polypeptide is a fusion protein comprising Tat and a fusion partner selected from an immunological tag and a polyhistidine tag.
3. The method of claim 1 , wherein said determining step is an immunological assay using an antibody specific for acetylated Tat.
4. A cell-free in vitro assay for identifying an agent that inhibits SIRT1 Tat deacetylase activity, the method comprising:
contacting a test sample with a test agent, wherein the test sample comprises a SIRT1 Tat deacetylase polypeptide, an acetylated Tat polypeptide and NAD + ; and
determining the level of acetylated Tat polypeptide in the test sample compared to the level of acetylated Tat polypeptide in a control sample lacking the test agent, wherein a reduction in the level of acetylated Tat polypeptide in the test sample compared to the control sample indicates that the test agent inhibits SIRT1 Tat deacetylase activity.
5. The method of claim 4 , wherein said determining step is an immunological assay using an antibody specific for acetylated Tat.
6. The method of claim 1 , wherein the cell is a eukaryotic cell.
7. The method of claim 6 , wherein the cell is a mammalian cell.
8. The method of claim 1 , wherein the cell is genetically modified to produce the SIRT1 polypeptide.
9. The method of claim 1 , wherein the cell is genetically modified to produce the Tat polypeptide.
10. The method of claim 1 , wherein the SIRT 1 Tat deacetylase polypeptide is a human SIRT1 Tat deacetylase polypeptide.
11. The method of claim 1 , wherein the Tat polypeptide comprises the amino acid sequence Lys-(Ala or Gly)-Leu-Gly-Ile-Ser-Tyr-Gly-Arg-Lys-Lys-Arg-(Arg or Lys)-(Gln or His)-Arg-Arg-(Arg or Gly or Lys or Ser)-(Pro or Ala or Thr)-(Gln or Pro or Thr) (SEQ ID NO:1), wherein one or more of the lysines is acetylated.
12. The method of claim 1 , wherein the Tat polypeptide comprises the amino acid sequence Ser-Tyr-Gly-Arg-AcLys-Lys-Lys-Arg-Arg-Gln-Arg (SEQ ID NO:2).
13. The method of claim 4 , wherein the SIRT1 Tat deacetylase polypeptide is a human SIRT1 Tat deacetylase polypeptide.
14. The method of claim 4 , wherein the Tat polypeptide comprises the amino acid sequence Lys-(Ala or Gly)-Leu-Gly-Ile-Ser-Tyr-Gly-Arg-Lys-Lys-Arg-(Arg or Lys)-(Gln or His)-Arg-Arg-(Arg or Gly or Lys or Ser)-(Pro or Ala or Thr)-(Gln or Pro or Thr) (SEQ ID NO:1), wherein one or more of the lysines is acetylated.
15. The method of claim 4 , wherein the Tat polypeptide comprises the amino acid sequence Ser-Tyr-Gly-Arg-AcLys-Lys-Lys-Arg-Arg-Gln-Arg (SEQ ID NO:2).
16. The method of claim 4 , wherein the SIRT1 polypeptide and the Tat polypeptide represent at least 80% by weight of the proteins in the sample.