IP Library Granted Patent US 9,463,216
Granted Patent B2
US 9,463,216 · App. 13/738,911 · Granted Oct 11, 2016

Poly-glutamic acid anti-anthrax compositions and methods for using the same

Inventors: Bryan A. Krantz (El Cerrito, CA); Alexander F. Kintzer (Berkeley, CA); Jakob H. von Moltke (Oakland, CA)
Assignee: The Regents of the University of California
A61K38/164A61K31/198A61K33/26A61K47/48315
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Quick Facts
Patent No.
US 9,463,216
App. No.
13/738,911
Granted
Oct 11, 2016
Kind
B2
Abstract

Methods and compositions for inhibiting entry of an anthrax toxin and/or an anthrax toxin protein into a cell are provided. Aspects of the subject methods include administering to a host an effective amount of poly-γ-Glutamic acid-Fe(III) chelate. Also provided are compositions suitable for use in the subject methods, as well as pharmaceutical preparations thereof.

Claims (10)

1. A method of inhibiting entry of an anthrax toxin protein into a cell, the method comprising:

contacting the cell with an effective amount of a poly-γ-Glutamic acid-Fe(III) chelate to inhibit entry of the anthrax toxin protein into the cell.

2. The method according to claim 1 , wherein the poly-γ-Glutamic acid of the poly-γ-Glutamic acid-Fe(III) chelate has a molecular weight of from about 200 to about 400 kDa.

3. The method according to claim 1 , wherein the poly-γ-Glutamic acid-Fe(III) chelate is a poly-γ-D-Glutamic acid-Fe(III) chelate.

4. The method according to claim 1 , wherein the poly-γ-Glutamic acid-Fe(III) chelate is a poly-γ-DL-Glutamic acid-Fe(III) chelate.

5. The method according to claim 4 , wherein the poly-γ-DL-Glutamic acid-Fe(III) chelate comprises about 25% to about 90% D-Glutamic acid and about 75% to about 10% L-Glutamic acid.

6. The method according to claim 5 , wherein the poly-γ-DL-Glutamic acid-Fe(III) chelate comprises about 25% D-Glutamic acid and about 75% L-Glutamic acid, and wherein the poly-γ-DL-Glutamic acid-Fe(III) chelate is resistant to digestion by B. anthracis γ-DPGA depolymerase enzyme (CapD).

7. The method according to claim 1 , wherein the anthrax toxin protein is selected from lethal factor (LF) and edema factor (EF).

8. The method according to claim 1 , wherein the method is in vitro.

9. The method according to claim 1 , wherein the method is in vivo.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 19, 2015
From: UNIVERSITY OF CALIFORNIA BERKELEY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036389/0929 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2013
From: KRANTZ, BRYAN A.; KINTZER, ALEXANDER F.; VON MOLTKE, JAKOB H.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 030200/0026 →
Continuity (2)
Provisional Application 61585183 · Jan 10, 2012
Related Publication 20150265674A1 · Sep 24, 2015