IP Library Granted Patent US 10,358,471
Granted Patent B2
US 10,358,471 · App. 16/249,540 · Granted Jul 23, 2019

Fusion proteins of collagen-binding domain and parathyroid hormone

Inventors: Robert C. Gensure (Lexington, MA); Joshua Sakon (Fayetteville, AR); Osamu Matsushita (Okayama, JP); Tulasi Ponnapakkam (Metairie, LA)
Assignees: The Board of Trustees of the University of Arkansas; Ochsner Clinic Foundation; National University Corporation Kagawa university
C07K14/635A61K8/64A61K8/66A61K9/0019A61K35/28A61K38/164A61K38/29A61K38/4886A61Q7/00C12N9/1088C12N9/50C12N9/52C12N9/6489C12Y205/01018C12Y304/24003C12Y304/24007A61K2800/86A61K2800/91C07K2319/00C07K2319/50C07K2319/70
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Quick Facts
Patent No.
US 10,358,471
App. No.
16/249,540
Granted
Jul 23, 2019
Kind
B2
Abstract

Fusion proteins containing active agonist or antagonist fragments of parathyroid hormone (PTH) and parathyroid hormone related peptide (PTHrP) coupled to a collagen-binding domain are presented. The fusion proteins can be used to promote bone growth, to promote hair growth, to prevent cancer metastasis to bone, to promote immune reconstitution with a bone marrow stem cell transplant, to promote mobilization of bone marrow stem cells for collection for autologous stem cell transplant, and to treat renal osteodystrophy. Pharmaceutical agents comprising a collagen-binding polypeptide segment linked to a non-peptidyl PTH/PTHrP receptor agonist or antagonist are also presented.

Claims (16)

1. A composition comprising:

a collagen-binding polypeptide segment covalently linked to a PTH/PTHrP receptor antagonist; wherein the collagen-binding polypeptide segment is a bacterial collagen binding polypeptide segment, wherein the PTH/PTHrP receptor antagonist comprises the polypeptide selected from the group consisting of residues 7-14 of SEQ ID NO: 7, residues 7-33 of SEQ ID NO: 7, residues 7-34 of SEQ ID NO: 7, SEQ ID NO: 11 and residues 7-34 of SEQ ID NO: 8, and wherein the collagen-binding polypeptide segment comprises the polypeptide selected from the group consisting of SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, polypeptides at least 90% identical to SEQ ID NOs 13-17 and fragments consisting of at least 10 consecutive amino acids of any one of SEQ ID NOs: 13-17.

2. The composition of claim 1 , wherein the collagen-binding polypeptide segment and the PTH/PTHrP receptor antagonist are chemically cross-linked to each other or are polypeptide portions of a fusion protein.

3. The composition of claim 1 , wherein the PTH/PTHrP receptor antagonist is a polypeptide and the N-terminus of the collagen-binding polypeptide segment is linked directly or through a linker polypeptide segment to the C-terminus of the PTH/PTHrP receptor antagonist polypeptide.

4. The composition of claim 1 , wherein the composition further comprises residues 37-130 of SEQ ID NO: 2 covalently linked to the collagen binding polypeptide segment.

5. The composition of claim 1 , wherein the collagen binding polypeptide segment comprises a polypeptide selected from the group consisting of SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, and SEQ ID NO: 17.

6. The composition of claim 1 , wherein the collagen binding polypeptide segment comprises polypeptides having at least 90% identity to SEQ ID NOs 13-17.

7. The composition of claim 1 , wherein the PTH/PTHrP receptor antagonist consists of a polypeptide selected from the group consisting of residues 7-14 of SEQ ID NO: 7, residues 7-33 of SEQ ID NO: 7, residues 7-34 of SEQ ID NO: 7 and residues 7-34 of SEQ ID NO: 8.

8. A method of promoting hair growth in a mammal comprising: administering the composition of claim 1 to the mammal in an amount effective to promote hair growth.

9. The method of claim 8 , wherein the composition is administered locally at the site of desired hair growth.

10. The method of claim 8 , wherein the administration is by subcutaneous or intradermal injection.

11. The method of claim 8 , wherein the mammal is afflicted with chemotherapy-induced alopecia.

12. A method of treating or reducing renal osteodystrophy in a mammal comprising administering the composition of claim 1 to the mammal in an amount effective to reduce renal osteodystrophy or renal disease in the mammal.

13. The method of claim 12 , wherein the composition is administered by injection.

14. A method of treating bone metastasis of cancer in a mammal comprising administering the composition of claim 1 to the mammal in an amount effective to reduce the incidence of bone metastasis of cancer or slow the growth of metastatic cancer in the bone in the mammal.

15. The method of claim 14 , wherein the composition is administered by injection.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2019
From: SAKON, JOSHUA
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS
Reel/Frame 050329/0402 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2019
From: PONNAPAKKAM, TULASI; GENSURE, ROBERT C.
To: OCHSNER CLINIC FOUNDATION
Reel/Frame 050329/0495 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2019
From: MATSUSHITA, OSAMU
To: NATIONAL UNIVERSITY CORPORATION KAGAWA UNIVERSITY
Reel/Frame 050329/0566 →
Continuity (6)
Continuation 15387817 · Dec 22, 2016
Continuation 14743629 · Jun 18, 2015
Division 13898058 · May 20, 2013
Division 12594547
Provisional Application 60922433 · Apr 9, 2007
Related Publication 20190135890A1 · May 9, 2019
Cited By (1)
US 12,403,179