Claims
- 1. An isolated polypeptide comprising one or more amino acid sequences selected from SEQ ID NO 1-SEQ ID NO 5 and SEQ ID NO: 7-SEQ ID NO: 11, said polypeptide having the ability to bind RANK.
- 2. A polypeptide of claim 1 having conservative or non-conservative modifications and still having the ability to bind to RANK.
- 3. A polypeptide comprising a RANKL sequence involved in binding to RANK, wherein said sequence consists essentially of one or more amino acid sequences selected from SEQ ID NO 1-SEQ ID NO 5 and SEQ ID NO: 7-SEQ ID NO: 11, and said polypeptide has the ability to bind to RANK.
- 4. The polypeptide of claim 3 having conservative or non-conservative modifications and having the ability to inhibit RANKL binding with RANK.
- 5. A polypeptide, other than RANKL, comprising one or more external surface loops of RANKL, said polypeptide having the ability to bind to RANK.
- 6. A polypeptide comprising one or more external surface loops of RANKL, said polypeptide having the ability to competitively inhibit RANKL binding with RANK.
- 7. The polypeptide of claim 1 consisting essentially of the amino acid sequence selected from SEQ ID NO 1-SEQ ID NO 5 and SEQ ID NO: 7-SEQ ID NO: 11.
- 8. A compound comprising a fragment, analog, mimic or derivative of the polypeptide of claim 1, 2, 3, 4, 5, 6, or 7, said compound having the ability to bind to RANK.
- 9. A pharmaceutical composition comprising an effective amount of the polypeptide of claim 1, 2, 3, 4, 5, 6, 7, in a pharmaceutically acceptable carrier, adjuvant, solubilizer, stabilizer, and/or anti-oxidant.
- 10. A pharmaceutical composition comprising an effective amount of the compound of claim 8 in a pharmaceutically acceptable carrier, adjuvant, solubilizer, stabilizer, and/or anti-oxidant.
- 11. A method of inhibiting osteoclast differentiation comprising administering an effective amount of the pharmaceutical composition of claim 9.
- 12. A method of inhibiting bone resorption comprising administering an effective amount of the pharmaceutical composition of claim 9.
- 13. A method of competitively inhibiting RANKL, said method comprising administering an effective amount of the compound of claim 1-8.
- 14. A method of competitively inhibiting RANKL, said method comprising administering an effective amount of the pharmaceutical composition of claim 9.
- 15. A method of treating diseases or conditions selected from the group comprising osteoporosis, juvenile osteoporosis, osteogenesis imperfecta, hypercalcemia, hyperparathyroidism, osteomalacia, osteohalisteresis, osteolytic bone disease, osteonecrosis, Paget's disease of bone, bone loss due to rheumatoid arthritis, inflammatory arthritis, osteomyelitis, corticosteroid treatment, metastatic bone diseases, periodontal bone loss, bone loss due to cancer, age-related loss of bone mass, and other forms of osteopenia, wherein the method comprises administering an effective amount of the pharmaceutical composition of claim 9.
- 16. The method of claim 15, wherein the diseases or conditions comprise osteoporosis, osteolytic bone disease, rheumatoid arthritis, and skeletal metastasis.
- 17. A polypeptide comprising (a) a RANKL sequence involved in binding to RANK, wherein said sequence consists essentially of at least one amino acid sequence selected from SEQ ID NO 1-SEQ ID NO 5 and SEQ ID NO: 7-SEQ ID NO: 11, and said polypeptide has the ability to bind to RANK; and (b) additional amino acid residues flanking said sequence that do not eliminate the ability of the sequence to bind RANK.
- 18. The polypeptide of claim 1 having one or more of the following modifications:
(i) one in which one or more amino acid residues of the polypeptide are substituted with a conserved or non-conserved amino acid residue, such residue may or may not be one encoded by the genetic code; (ii) one in which one or more of the amino acid residues includes a substituent group; (iii) one in which the polypeptide is fused to another compound such as a compound to increase the half-life of the protein; (iv) one in which additional amino acids are fused to the polypeptide to aid in purification or in detection and identification; or (v) one in which additional amino acid residues are fused to the polypeptide to aid in modifying tissue distribution or localization of the protein to certain locations such as the cell membrane or extracellular compartments.
- 19. A method of screening for RANKL-binding compounds, said method comprising performing a binding assay between a test compound, a reference compound and RANK wherein said reference compound consists essentially of a polypeptide of at least one amino acid sequence selected from SEQ ID NO 1-SEQ ID NO 5 and SEQ ID NO: 7-SEQ ID NO: 11.
- 20. A polynucleotide encoding the polypeptide of claim 1.
- 21. A polynucleotide of claim 20 which exhibit regular degeneracy in accordance with the degeneracy of the genetic code.
- 22. A polynucleotide of claim 20 encoding a polypeptide exhibiting conservative substitutions to the polypeptide of claim 1.
- 23. An expression vector comprising the polynucleotide of claim 20, 21, or 22.
- 24. A host cell containing an expression vector of claim 23.
- 25. The method of treating diseases of claim 15 further comprising administering an effective amount of one or more pharmaceutical compositions for enhancing bone growth to a subject in need thereof.
Parent Case Info
[0001] This application is related to and claims the benefit of the following U.S. applications, which are incorporated herein by reference: Ser. No. 60/277,855 filed Mar. 22, 2001; Ser. No. 10/105,057 filed Mar. 22, 2002; Ser. No. 60/311,163 filed Aug. 9, 2001; Ser. No. 10/215,446 filed Aug. 9, 2002; Ser. No. 60/329,231 filed Oct. 12, 2001; Ser. No. 60/329,393 filed Oct. 15, 2001; Ser. No. 60/329,360 filed Oct. 15, 2001; Ser. No. 60/328,876 filed Oct. 12, 2001; U.S. non-provisional entitled RANKL Mimics and Uses Thereof, Lam, et al. filed Oct. 15, 2002; and U.S. non-provisional entitled Methods for Screening Osteogenic Compounds, Lam, et al. filed Oct. 15, 2002.
Government Interests
[0002] This invention was made in part with Government support under National Institutes of Health Grants AR32788, AR46123 and DE05413. The Government has certain rights in the invention.
Provisional Applications (4)
|
Number |
Date |
Country |
|
60329360 |
Oct 2001 |
US |
|
60329231 |
Oct 2001 |
US |
|
60329393 |
Oct 2001 |
US |
|
60328876 |
Oct 2001 |
US |