Treatment of liver disorders by administration of RAP conjugates
View Patent ↗The present invention relates to the use of receptor-associate protein (RAP) and fragments and variants thereof to improve delivery of therapeutic compounds to the liver and provides methods to treat liver disorders and conditions, such as hepatic carcinoma, by administering RAP or RAP variants conjugated to active agents.
1. A method of delivering an active agent to the liver of a subject in need of an agent for treating a liver disorder comprising:
administering to said animal a conjugate comprising (a) a receptor binding moiety selected from the group consisting of Receptor Associated Protein of SEQ ID NO: 1 (RAP), a RAP fragment, and a RAP variant that retains RAP's binding affinity to LRP1 of about 1-5 nM, attached to (b) an active agent, wherein said RAP fragment or variant comprises an amino acid sequence at least 80% identical to SEQ ID NO: 4 and wherein said agent is delivered to the liver.
2. The method of claim 1 wherein the receptor binding moiety of said conjugate is a RAP fragment or variant missing at least 200 and up to 243 amino acids from the N-terminus of SEQ ID NO: 1.
3. The method of claim 1 wherein the receptor binding moiety of said conjugate is a RAP fragment missing at least 200 and up to 243 amino acids from the N-terminus of SEQ ID NO: 1.
4. The method of claim 2 or 3 wherein said RAP fragment or variant is missing 243 amino acids from the N-terminus of SEQ ID NO: 1.
5. The method of claim 2 or 3 wherein said RAP fragment or variant is further missing at least 4 and up to 11 amino acids from the C-terminus of SEQ ID NO: 1.
6. The method of claim 2 or 3 wherein said RAP fragment or variant is further missing 11 amino acids from the C-terminus of SEQ ID NO: 1.
7. The method of claim 1 wherein said RAP fragment or variant lacks amino acids 1-143 and 320-323 of mature RAP of SEQ ID NO: 1.
8. The method of claim 2 or 3 wherein said RAP fragment or variant comprises a continuous portion of RAP d3 (SEQ ID NO: 2) that is (a) at least 71 amino acids in length and (b) comprises amino acids 256-270.
9. The method of claim 1 wherein said receptor binding moiety is a cyclic RAP peptide that is less than 85 amino acids in length, comprising 50 contiguous amino acids that are at least 70% identical to SEQ ID NO: 4, and which binds to LRP1 with a Kd of about 1×10-8 M or less.
10. The method of claim 1 wherein said receptor binding moiety is a RAP variant, said RAP variant comprising one or more conservative substitutions relative to native RAP of SEQ ID NO: 1.
11. The method of claim 1 wherein said receptor binding moiety is a RAP variant, said RAP variant comprising a mutation at any one of positions 217, 249, or 251 of mature RAP.
12. The method of claim 2 or 3 wherein said RAP variant comprises a mutation, wherein said mutation is the replacement of an acidic amino acid with a basic amino acid.
13. The method of claim 12 wherein said acidic amino acid is selected from the group consisting of D and E.
14. The method of claim 12 , wherein said basic amino acid is selected from the group consisting of K and R.
15. The method of claim 2 or 3 wherein said RAP variant comprises a mutation, wherein said mutation is the replacement of a basic amino acid with an acidic amino acid.
16. The method of claim 15 , wherein said basic amino acid is selected from the group consisting of K and R.
17. The method of claim 15 , wherein said acidic amino acid is selected from the group consisting of D and E.
18. The method of claim 1 wherein said RAP variant comprises a mutation, 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.
19. The method of claim 1 wherein the receptor binding moiety of said conjugate is a RAP fragment or variant set out in SEQ ID NO: 9.
20. The method of claim 1 , wherein the RAP, RAP fragment or RAP variant and diagnostic or therapeutic agent are linked through a linker.
21. The method of claim 20 , wherein said linker is a peptide linker.
22. The method of claim 1 wherein the receptor binding moiety is an oligomeric combination of RAP fragments or RAP variants.
23. The method of claim 1 wherein the conjugate is in a pharmaceutical composition comprising a pharmaceutically acceptable carrier, diluent or excipient.
24. The method of claim 1 wherein the active agent is a cytotoxic agent.
25. The method of claim 24 wherein the cytotoxic agent is selected from the group consisting of Mechlorethamine hydrochloride, Cyclophosphamide, Ifosfamide, Chlorambucil, Melphalan, Busulfan, Thiotepa, Carmustine, Lomustine, Dacarbazine and Streptozocin.
26. The method of claim 1 wherein the active agent is a radioisotope.
27. The method of claim 26 wherein the radioisotope is selected from the group consisting of 131I, 125I, 111In, 90Y, 67Cu, 127Lu, 212Bi, 213Bi, 255Fm, 149Tb, 223Rd, 213Pb, 212Pb, 211At, 89Sr, 153Sm, 166Ho, 225Ac, 186Re, 67Ga, 68Ga and 99 mTc.