IP Library › Granted Patent US 11,000,571
Granted Patent B2
US 11,000,571 · App. 15/632,638 · Granted May 11, 2021

Modified fragments from the octarepeat region of prion protein as hemin binders

Inventor: Ewa Anna Bienkiewicz (Tallahassee, FL)
Assignee: Florida State University Research Foundation, Inc.
A61K38/177
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Quick Facts
Patent No.
US 11,000,571
App. No.
15/632,638
Granted
May 11, 2021
Kind
B2
Abstract

An example of the composition incudes at least one amino acid sequence from the octarepeat region of hemin that is modified by substituting at least one proline (P) residue in the amino acid sequence. The composition is effective to bind with hemin and for treating hemorrhagic injury.

Claims (17)

1. A composition comprising at least one isolated amino acid sequence selected from SEQ ID NOs: 2, 3, 4, 5, and 6 in which at least one proline (P) residue in the amino acid sequence is substituted by an amino acid having the formula

wherein R1 is a methyl group and R2 is an alkyl functional group having 1 to 4 carbon atoms.

2. The composition of claim 1 , wherein R2 is selected from a methyl, ethyl, butyl, and propyl group.

3. The composition of claim 1 , wherein R2 is a methyl group.

4. The composition of claim 1 , wherein the composition is within a pharmaceutical dosage form.

5. A method of binding hemin, the method comprising administering to a hemin solution a composition comprising at least one isolated amino acid sequence selected from SEQ ID NOs: 2, 3, 4, 5, and 6 in which at least one proline (P) residue in the amino acid sequence is substituted by an amino acid having the formula

wherein R1 is a methyl group and R2 is an alkyl functional group having 1 to 4 carbon atoms; and

wherein the isolated amino acid sequence is effective for binding to hemin in the hemin solution.

6. The method of claim 5 , wherein R2 is selected from a methyl, ethyl, butyl, and propyl group.

7. The method of claim 5 , wherein R2 is a methyl group.

8. The method of claim 5 , wherein the composition is within a pharmaceutical dosage form.

9. A method of treating a hemorrhagic injury, the method comprising administering to a patient in need thereof a therapeutically effective composition comprising at least one isolated amino acid sequence selected from SEQ ID NOs: 2, 3, 4, 5, and 6 in which at least one proline (P) residue in the amino acid sequence is substituted by an amino acid having the formula

wherein R1 is a methyl group and R2 is an alkyl functional group having 1 to 4 carbon atoms.

10. The method of claim 9 , wherein R2 is selected from a methyl, ethyl, butyl, and propyl group.

11. The method of claim 9 , wherein R2 is a methyl group.

12. The method of claim 9 , wherein the composition is within a pharmaceutical dosage form.

13. The method of claim 9 , wherein the hemorrhagic injury is at least one hemorrhagic injury selected from the group consisting of stroke and traumatic brain injury.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2017
From: BIENKIEWICZ, EWA ANNA
To: FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC.
Reel/Frame 042818/0141 →
Continuity (2)
Provisional Application 62354957 · Jun 27, 2016
Related Publication 20170368137A1 · Dec 28, 2017