IP Library Granted Patent US 7,994,278
Granted Patent B1
US 7,994,278 · App. 09/632,831 · Granted Aug 9, 2011

Biologically active polypeptides derived from a novel early stage pregnancy factor designated maternin (MA)

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Quick Facts
Patent No.
US 7,994,278
App. No.
09/632,831
Granted
Aug 9, 2011
Kind
B1
Abstract

The invention relates to therapeutic polypeptides isolated from beta-human chorionic gonadotropin (β-hCG) found in human early pregnancy urine, now synthetically produced and designated Maternin. The therapeutic polypeptides and their functional equivalents are useful in treating and/or preventing various medical conditions. Examples of therapeutic effects of the therapeutic polypeptides include anti-HIV, anti-cancer, anti-wasting, prohematopoietic (e.g., anemias, radiation-mediated bone marrow damage, and trauma-mediated blood loss), and anti-angiogenic effects. The invention also provides pharmaceutical compositions comprising the therapeutic polypeptides, as well as methods for using the therapeutic polypeptides, functional equivalents and/or pharmaceutical compositions in the treatment and/or prevention of such medical conditions.

Claims (20)

1. An isolated polypeptide consisting of SEQ ID NO: 2 or a truncated form of SEQ ID NO: 2 selected from the group consisting of SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 7 and SEQ ID NO: 9.

2. An isolated polypeptide wherein the polypeptide comprises the amino acid sequence of the MA peptide (SEQ ID NO: 2) with the proviso that the polypeptide does not comprise amino acid extensions corresponding to amino terminus or carboxy terminus amino acid sequences along the β-hCG chain (SEQ ID NO: 1) contiguous to the amino acid sequence of the MA peptide (SEQ ID NO: 2).

3. An isolated polypeptide consisting of a truncated form of SEQ ID NO: 2, wherein the truncated form has 1, 2, 3, 4, 5 or 6 amino acid residues deleted from the amino terminus or carboxy terminus of SEQ ID NO: 2.

4. A fusion polypeptide comprising the polypeptide of claim 1 joined via a covalent bond to a heterologous polypeptide.

5. A fusion polypeptide comprising two or more of the polypeptides of claim 1 joined together via a covalent bond.

6. A pharmaceutical composition comprising the polypeptide of claim 1 in association with a pharmaceutically acceptable carrier.

7. A peptide isolated from early pregnancy urine consisting essentially of the amino acid sequence of MA (SEQ ID NO: 2) with the proviso that the peptide does not comprise amino acid extensions corresponding to amino terminus or carboxy terminus amino acid sequences along the β-hCG chain (SEQ ID NO: 1) contiguous to the amino acid sequence of the MA peptide (SEQ ID NO: 2).

8. A fusion polypeptide comprising the polypeptide of claim 2 joined via a covalent bond to a heterologous polypeptide.

9. A fusion polypeptide comprising two or more of the polypeptides of claim 2 joined together via a covalent bond.

10. A pharmaceutical composition comprising the polypeptide of claim 2 in association with a pharmaceutically acceptable carrier.

11. A fusion polypeptide comprising the polypeptide of claim 3 joined via a covalent bond to a heterologous polypeptide.

12. A fusion polypeptide comprising two or more of the polypeptides of claim 3 joined together via a covalent bond.

13. A pharmaceutical composition comprising the polypeptide of claim 3 in association with a pharmaceutically acceptable carrier.

14. A fusion polypeptide comprising the peptide of claim 7 joined via a covalent bond to a heterologous polypeptide.

15. A fusion polypeptide comprising two or more of the peptides of claim 7 joined together via a covalent bond.

16. A pharmaceutical composition comprising the peptide of claim 7 in association with a pharmaceutically acceptable carrier.

17. An isolated polypeptide consisting essentially of the amino acid sequence of MA (SEQ ID NO: 2) with the proviso that the peptide does not comprise amino acid extensions corresponding to amino terminus or carboxy terminus amino acid sequences along the β-hCG chain (SEQ ID NO: 1) contiguous to the amino acid sequence of the MA peptide (SEQ ID NO: 2).

18. A fusion polypeptide comprising the polypeptide of claim 17 joined via a covalent bond to a heterologous polypeptide.

19. A fusion polypeptide comprising two or more of the polypeptides of claim 17 joined together via a covalent bond.

20. A pharmaceutical composition comprising the polypeptide of claim 17 in association with a pharmaceutically acceptable carrier.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 8, 2009
From: UNIVERSITY OF MARYLAND BIOTECHNOLOGY INSTITUTE
To: LUNARDI-ISKANDAR, PH.D., YANTO, M.D.
Reel/Frame 023621/0684 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 8, 2009
From: LUNARDI-ISKANDAR, PH.D., YANTO, M.D.
To: NOBEL BIOSCIENCES LLC
Reel/Frame 023621/0826 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2004
From: REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE
To: EUV LLC
Reel/Frame 014601/0343 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 25, 2002
From: GALLO, ROBERT; BRYANT, JOSEPH; LUNARDI-ISKANDAR, YANTO
To: MARYLAND BIOTECHNOLOGY INSTITUTE, UNIVERSITY OF
Reel/Frame 012756/0358 →