Compositions comprising receptor-associated protein (RAP) variants specific for CR-containing proteins and uses thereof
View Patent ↗The present invention relates generally to receptor-selective variants of the low-density lipoprotein receptor-associated protein (RAP) and compositions thereof, methods of generating such variants and methods of using such receptor-selective RAP variant compositions for therapeutic purposes.
1. An isolated polypeptide comprising an amino acid sequence variant of the alpha-2-macroglobulin/low density lipoprotein receptor-related protein-associated protein 1 (RAP), wherein said RAP variant binds selectively to a pair of complement-type repeats within a protein, with an affinity that is at least 3-fold greater than the affinity of wild-type RAP for the same pair of complement-type repeats, and wherein said RAP variant consists of an amino acid sequence that lacks amino acids 1-143 and 320-323 of a mature RAP set forth in SEQ ID NO: 121, has an amino acid sequence at least 95% identical to the corresponding portion of SEQ ID NO: 121, and contains at least one mutation within positions 205-250 of RAP set forth in SEQ ID NO: 121 or at least one mutation within positions 271-319 of RAP set forth in SEQ ID NO: 121.
2. The polypeptide of claim 1 , wherein said CR-containing protein is selected from the group consisting of LDLR (P01130), LRP1 (P98157), LRP1B (Q9NZR2), LRP2 (P98164), LRP3 (075074), LRP4 (075096), LRP5 (075197), LRP6 (075581), LRP8 (Q14114), Sortilin (Q92673), LRP10 (Q7Z4F1), LRP11 (Q86VZ4), LRP12 (Q9Y561), FDC-D86 (CD320), VLDLR (P98155), TADG-15 (ST14, Q8WVC1), TMPS3 (P57727), TMPS4 (Q9NRS4), TMPS6 (Q8IU80), Q6ICC2, Q6PJ72, Q76B61, Q7RTY8, Q7Z7K9, Q86YD5, Q8NAN7, Q8NBJ0, Q8WW88, Q96NT6, Q9BYE1, Q9BYE2, Q9NPF0 and corin (Q8IZR7).
3. The polypeptide of claim 1 wherein the variant binds selectively to a protein selected from the group consisting of a matriptase protein, a VLDLR protein and an FDC-8D6 (CD320) protein.
4. The polypeptide according to claim 1 , wherein said mutation is the replacement of an acidic amino acid with a basic amino acid.
5. The polypeptide according to claim 1 , wherein said mutation is the replacement of a basic amino acid with an acidic amino acid.
6. The polypeptide according to claim 1 , wherein said mutation is the replacement of an amino acid selected from the group consisting of A, C, D, E, G, I, K, L, M, N, P, Q, R, S, T, and V with an amino acid selected from the group consisting of F, Y, W, and H.
7. The polypeptide of claim 1 , wherein said RAP variant comprises a mutation at two or more of the following positions set forth in SEQ ID NO: 121: 175, 205, 213, 217, 226, 230, 232, 239, 246, 249, 251, 256, 257, 261, 266, 267, 268, 270, 273, 287, 290, 294, 296, 297, 298, 305, 312, 313.
8. A polypeptide consisting of oligomeric combinations of polypeptides of claim 1 with multivalent binding properties defined by each polypeptide of the combination.
9. A compound comprising the polypeptide according to claim 1 conjugated to a diagnostic or therapeutic agent.
10. The compound of claim 9 , wherein the polypeptide and diagnostic or therapeutic agent are linked through a linker.
11. The compound of claim 10 , wherein said linker is a peptide linker.
12. A pharmaceutical composition comprising a compound of claim 9 in a pharmaceutically acceptable carrier, diluent or excipient.