Mutant proline-and-arginine rich peptides and methods for using the same
View Patent ↗The present invention relates to mutant proline-and-arginine rich (PR) peptides with defined structural characteristics for use in inhibiting mammalian 20S proteasome activity and modulating expression of genes regulating the NF-κB pathway. Mutant PR peptides of the present invention differ from wild-type PR peptides by having at least one to three amino acid substitutions, wherein at least one of the amino acid residues at position one, two or three of the mutant PR peptide is positively charged.
1. An isolated mutant proline-and-arginine-rich (PR) peptide, wherein said peptide is 11 amino acid residues in length, has a hydrophobic amino acid residue at position eight, and has one to three amino acid substitutions in the amino acid sequence set forth in SEQ ID NO:2, wherein at least one of the amino acid residues at position one, two, or three is positively charged and wherein said peptide exhibits an increase in activity to inhibit 20S proteosome activity compared to the PR peptide of SEQ ID NO:2.
2. An isolated mutant proline-and-arginine-rich (PR) peptide consisting of 12 amino acid residues in length, said peptide having a C-terminal tryptophan, a hydrophobic amino acid residue at position eight, and having one to three amino acid substitutions in the amino acid sequence set forth in SEQ ID NO:2, wherein at least one of the amino acid residues at position one, two, or three is positively charged and wherein said peptide exhibits an increase in activity to inhibit 20S proteasome activity compared to the PR peptide of SEQ ID NO:2.
3. The isolated mutant PR peptide of claim 1 , wherein at least two of the amino acid residues at positions one, two, or three are positively charged and the amino acid residue at position eight is not negatively charged.
4. The isolated mutant PR peptide of claim 1 , wherein the amino acid residue at position four is proline.
5. An isolated mutant PR peptide consisting of the amino acid sequence set forth in SEQ ID NO:4.
6. An isolated mutant PR peptide consisting of the amino acid sequence set forth in SEQ ID NO:5.
7. A method for inhibiting mammalian 20S proteasome activity comprising contacting a cell with the mutant PR peptide of claim 3 thereby inhibiting 20S proteasome activity in the cell.
8. A method for inhibiting mammalian 20S proteasome activity comprising contacting a cell with the mutant PR peptide of claim 5 thereby inhibiting 20S proteasome activity in the cell.
9. A method for inhibiting mammalian 20S proteasome activity comprising contacting a cell with the mutant PR peptide of claim 6 thereby inhibiting 20S proteasome activity in the cell.