Inhibitors of anaphase promoting complex activity
The invention provides an anti-proliferative composition comprising a non-peptide analog of the C-terminal isoleucine-arginine (IR) tail motif of an activator of an anaphase promoting complex (APC). The invention further provides methods of inhibiting the ubiquitination activity of the APC by administering compositions of the invention.
1. A method for inhibiting a ubiquitination activity of an APC in a mammalian cell comprising a spindle assembly checkpoint (SAC), comprising administering an effective amount of a non-peptide analog of a C-terminal IR motif of an activator of an APC to a mammalian cell to inhibit a degradation of a substrate of an APC.
2. A method for inhibiting a ubiquitination activity of an APC in a mammalian cell comprising a spindle assembly checkpoint (SAC), comprising administering an effective amount of a non-peptide analog of a C-terminal IR motif of an activator of an APC to a mammalian cell to induce a cell cycle checkpoint.
3. The method of claim 1 or 2 , wherein said analog is tosyl-L-arginine methylester (TAME).
4. The method of claim 1 or 2 , wherein said analog is tosyl-L-arginine methylester (TAME), tosyl-L-arginine amide (TAA), tosyl-L-lysine methylester (TLME), tosyl-L-arginine (TAOH), acetyl-L-arginine methylester (AAME), Benzoyl-L-arginine amide (BAA), tosyl-L-arginine t-butyl-ester (TATE), or Benzoyl-L-arginine methylester (BAME).
5. The method of claim 1 , wherein said cell is human.
6. The method of claim 1 , wherein said analog contacts a component of a tetratricopeptide repeats (TPR) subcomplex of an APC.
7. The method of claim 6 , wherein said component of a TPR subcomplex is APC3/Cdc27, APC6, APC7, or APC8.
8. The method of claim 2 , wherein said cell cycle checkpoint is a spindle assembly checkpoint (SAC).
9. The method of claim 1 or 2 , wherein said activator of an APC is Cdc20 or Cdh1.