IP Library Granted Patent US 10,808,228
Granted Patent B2
US 10,808,228 · App. 15/865,713 · Granted Oct 20, 2020

Methods for increasing the infectivity of viruses utilizing alkyne-modified fatty acids

Inventors: Brian Agnew (Carlsbad, CA); David Graham (Baltimore, MD)
Assignees: THE JOHNS HOPKINS UNIVERSITY; LIFE TECHNOLOGIES CORPORATION
C12N7/00A61K39/00A61K48/00C12N2740/16034C12N2740/16045C12N2740/16051C12N2810/10
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Quick Facts
Patent No.
US 10,808,228
App. No.
15/865,713
Granted
Oct 20, 2020
Kind
B2
Abstract

Methods of using viruses labeled with alkyne-modified biomolecules, such as fatty acids, carbohydrates and lipids, to treat a plant, an insect or an animal infected with a virus or to increase the infectivity of a virus, such as the human immunodeficiency virus, are provided. Also provided are methods of labeling a virus, such as human immunodeficiency virus, with an alkyne-modified biomolecule, such as a fatty acid, a carbohydrate, or an isoprenoid lipid. The viruses labeled with alkyne-modified biomolecules may be combined with a pharmaceutically acceptable excipient to produce a pharmaceutical composition, optionally containing another anti-viral agent and/or a delivery agent, such as a liposome.

Claims (15)

1. A human immunodeficiency virus comprising an alkyne-modified fatty acid moiety, wherein the moiety is non-naturally occurring, and

wherein the alkyne-modified fatty acid moiety is 15-ethynylpentadecanyl or 12-ethynyldodecanyl.

2. The virus of claim 1 , wherein the virus is HIV-1.

3. The virus of claim 1 , wherein the virus is inactivated.

4. The virus of claim 1 , wherein the virus is attenuated.

5. The virus of claim 1 , wherein the alkyne-modified fatty acid moiety is 15-ethynylpentadecanyl.

6. The virus of claim 1 , wherein the alkyne-modified fatty acid moiety is attached to the virus by an amide or a thioester bond.

7. A composition comprising the virus of claim 1 .

8. The composition of claim 7 , further comprising a pharmaceutically acceptable excipient.

9. The virus of claim 1 , wherein the alkyne-modified fatty acid moiety is 12-ethynyldodecanyl.

10. An in vitro method of producing the human immunodeficiency virus of claim 1 , the method comprising contacting the virus with the alkyne-modified fatty acid moiety in an amount effective to enhance the infectivity of the virus.

11. The method of claim 10 , wherein the virus is in a cell.

12. The method of claim 11 , wherein the cell is a human animal cell or a non-human animal cell.

13. The method of claim 10 , wherein the human immunodeficiency virus is HIV-1.

14. The method of claim 10 , wherein the contacting is performed in a solution comprising at least one of animal serum, amino acids, buffers, fatty acids, glucose, hormones, inorganic salts, lipids, metal ion chelators, peptides, surfactants, trace metals, and vitamins.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2018
From: AGNEW, BRIAN
To: LIFE TECHNOLOGIES CORPORATION
Reel/Frame 044573/0724 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2018
From: GRAHAM, DAVID
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 045028/0450 →
Continuity (3)
Division 14374404
Provisional Application 61591047 · Jan 26, 2012
Related Publication 20180171306A1 · Jun 21, 2018