ENGINEERED PROTEINS INCLUDING MUTANT FIBRONECTIN DOMAINS

• US 20120270797A1
• Filed: 08/13/2010
• Published: 10/25/2012
• Est. Priority Date: 08/13/2009
• Status: Abandoned Application

• Current Assignee: Massachusetts Institute of Technology
• Original Assignee: Massachusetts Institute of Technology
• Inventors: Wittrup, Karl Dane, Spangler, Jamie B., Hackel, Benjamin Joseph
• Application Number:
  US13/390,086
• Publication Number:
  US 20120270797A1
• Time in Patent Office: Days
• US Class Current: 514/19.3
• CPC Class Codes: A61K 38/00 Medicinal preparations containing peptides peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: C07K 14/78 Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin or cold insoluble globulin [CIG]
• CPC Class Codes: C07K 2318/20 Antigen-binding scaffold molecules wherein the scaffold is not an immunoglobulin variable region or antibody mimetics

Abstract

The present invention features engineered proteins that can include a genetically modified Fn domain; two or more such domains joined to one another; or at least one genetically modified Fn domain joined to a target-specific protein scaffold. One or more accessory sequences can be included in or added to any of these configurations. Methods of use, including methods of treating cancer, with the engineered proteins are also disclosed.

Claims

1. An engineered protein comprising a first genetically modified fibronectin domain that binds a first epitope on a molecular target and a second genetically modified fibronectin domain that binds a second epitope on the target.

2. The engineered protein of claim 1, further comprising a linker between the first fibronectin domain and the second fibronectin domain.

3. The engineered protein of claim 2, wherein the linker is a polypeptide.

6. The engineered protein of claim 1, further comprising a heterologous protein.

7. The engineered protein of claim 6, wherein the heterologous protein is a target-specific protein scaffold.

8. The engineered protein of claim 7, wherein the target-specific protein scaffold is an immunoglobulin or a biologically active fragment or other variant thereof.

9. The engineered protein of claim 8, wherein the immunoglobulin is the antibody cetuximab or the antibody panitumumab.

10. The engineered protein of claim 7, wherein the target-specific protein scaffold is a designed ankyrin repeat protein, an anticalin, or an affibody.

11. The engineered protein of claim 1, further comprising an accessory sequence.

12. The engineered protein of claim 11, wherein the accessory sequence is an amino acid sequence that prolongs the circulating half-life of the genetically modified Fn domain or an engineered protein of which it is a part;

an amino acid sequence that facilitates isolation or purification of the engineered protein;

an amino acid sequence that facilitates the bond between one part of the engineered protein and another or between the engineered protein and another moiety;

an imaging agent or an amino acid sequence that can be detected and thereby serves as a label, marker, or tag;

or an amino acid sequence that is toxic.

13. The engineered protein of claim 12, wherein the amino acid sequence that prolongs the circulating half-life is an Fc region of an immunoglobulin, albumin, another plasma protein, or fragments or variants thereof of a length sufficient to prolong the circulating half-life of the engineered protein.

14. The engineered protein of claim 12, wherein the polypeptide that facilitates isolation or purification of the engineered protein is a green fluorescent protein (GFP), glutathione S-transferase (GST), c-myc, hemagglutinin, β

galactosidase, or Flag™

tag (Kodak) sequence.

15. The engineered protein of claim 12, wherein the moiety is a therapeutic compound.

16. The engineered protein of claim 1, wherein the first fibronectin domain and the second fibronectin domain are identical within their constant regions.

17. The engineered protein of claim 1, wherein the first fibronectin domain and the second fibronectin domain are at least 80% identical.

18. The engineered protein of claim 1, wherein the first fibronectin domain and/or the second fibronectin domain is a tenth type III fibronectin domain.

19. The engineered protein of claim 1, wherein the first fibronectin domain and/or the second fibronectin domain comprises a human fibronectin sequence.

20. The engineered protein of claim 1, wherein the first fibronectin domain and/or the second fibronectin domain comprises clone A, clone B, clone C, clone D, or clone E.

21. The engineered protein of claim 1, wherein the target is a cellular receptor.

22. The engineered protein of claim 21, wherein the cellular receptor is a receptor tyrosine kinase of the ErbB, insulin, PDGF, FGF, VEGF, HGF, Trk, Eph, AXL, LTK, TIE, ROR, DDR, RET, KLG, RYK, or MuSK receptor family.

23. The engineered protein of claim 22, wherein the cellular receptor is an EGF receptor.

24. A nucleic acid comprising a sequence encoding the engineered protein of claim 1.

25. A vector comprising the nucleic acid sequence of claim 24.

26. The vector of claim 25, wherein the vector is a plasmid or a cosmid or other viral vector.

27. A cell ex vivo comprising the vector of claim 26.

28. A pharmaceutically acceptable composition comprising the engineered protein of claim 1.

29. A method of treating a patient who has cancer, the method comprising identifying a patient in need of treatment and administering to the patient a therapeutically effective amount of the pharmaceutically acceptable composition of claim 28, wherein the engineered protein specifically binds at least one epitope on a protein whose expression or activity is associated with the cancer.

4-5. -5. (canceled)

30. An engineered protein comprising (a) a genetically modified fibronectin domain that specifically binds a first epitope on a receptor tyrosine kinase and (b) a heterologous protein that specifically binds a second epitope on the tyrosine kinase receptor.

31. The engineered protein of claim 30, wherein the first epitope and the second epitope are non-overlapping.

32. The engineered protein of claim 30, wherein the genetically modified fibronectin domain is a mutant of a type III fibronectin domain.

37. The engineered protein of claim 30, wherein the heterologous protein is a target-specific protein scaffold.

41. The engineered protein of claim 30, further comprising an accessory sequence.

48. A nucleic acid comprising a sequence encoding the engineered protein of claim 30.

49. A vector comprising the nucleic acid sequence of claim 48.

51. A cell comprising the vector of claim 49.

52. A pharmaceutically acceptable composition comprising the engineered protein of claim 30.

53. A method of treating a patient who has cancer, the method comprising identifying a patient in need of treatment and administering to the patient a therapeutically effective amount of the pharmaceutically acceptable composition of claim 52, wherein the engineered protein specifically binds at least one epitope on a protein whose expression or activity is associated with the cancer.

33-36. -36. (canceled)

38-40. -40. (canceled)

42-47. -47. (canceled)

50. (canceled)

54-55. -55. (canceled)