Inhibitors of the trypsin-like site of the proteasome and methods of use thereof
The present invention is an inhibitor of the trypsin-like β2/β2i sites of the proteasome. The inhibitor is characterized as being a peptide-based epoxyketone or vinyl sulfone that contains an arginine or 4-aminomethylene-L-phenylalanine at the C-terminus (i.e., at the P1 position). Methods for using the inhibitor to inhibit the activity of the β2/β2i site of a proteasome and treat a proteasome-mediated disease or condition are also described.
1. A peptide-based inhibitor of the proteasome β2/β2i site comprising the structure:
(Y)-(X4)-X3-X2-X1 (SEQ ID NO:2),
wherein X1 is an arginine residue with an epoxyketone or vinyl sulfone warhead or X1 is a 4-aminomethylene-L-phenylalanine residue with an epoxyketone or vinyl sulfone warhead; X2 is Leu or Ser, X3 is Leu, Val, Arg, or 4-aminomethylene-L-Phe, wherein X4 is present or absent and when present is Phe; and Y is present or absent and when present is a capping group.
2. The peptide-based inhibitor of claim 1 , wherein the capping group is a label.
3. A pharmaceutical composition comprising the peptide-based inhibitor of claim 1 and a pharmaceutically acceptable carrier.
4. The pharmaceutical composition of claim 3 , further comprising an inhibitor of the proteasome β5/β5i site.
5. A method for inhibiting the activity of the β2/β2i site of a proteasome comprising contacting a proteasome with a peptide-based inhibitor of claim 1 so that activity of the proteasome β2/β2i site is inhibited.
6. A method for treating cancer,
organ graft rejection, an auto-immune disease, parasitic disease or inflammatory condition comprising administering to a subject in need of treatment an effective amount of the pharmaceutical composition of claim 3 thereby treating the subject's cancer, organ graft rejection, an auto-immune disease, parasitic disease or inflammatory condition.
7. The method of claim 6 , further comprising administering an inhibitor of the proteasome β5/β5i site.
8. A method for producing the peptide based inhibitor of claim 1 , comprising
(a) protecting amine groups of arginine or a 4-aminomethylene-L-phenyalanine residue,
(b) introducing an epoxyketone or vinyl sulfone warhead onto the arginine or 4-aminomethylene-L-phenylalanine residue, and
(c) attaching a proteasomal β2/β2i site-selective oligopeptide to the alpha amino-group of the arginine or 4-aminomethylene-L-phenylalanine so that a peptide-based inhibitor is produced.