Methods and compositions for protein delivery
The present invention provides methods and compositions for protein delivery. The invention features virus like particles, methods of making virus like particles and methods of using virus like particles to deliver proteins to a cell, to provide protein therapy and to treat diseases or disorders. The invention also features methods of targeting a protein to a cell, methods of protein therapy and methods of treating diseases or disorders using a TUS protein, a NLS or NES identified from full length TUS.
1. A virus-like particle (VLP) comprising:
a Gag fusion protein, wherein the Gag fusion protein comprises a matrix protein, a capsid protein, a nucleocapsid protein, covalently linked to a protein of interest selected from the group consisting of a cytotoxic enzyme, an interferon, a tumor suppressor, a recombinase, a hormone, and a stem cell transcription factor; and
a fusogenic protein having reduced ligand-binding activity,
wherein the Gag fusion protein does not comprise a reverse transcriptase, a protease, or an integrase.
2. The VLP of claim 1 , wherein the fusogenic protein is selected from the group consisting of: an influenza haemagglutinin, a respiratory syncytial virus fusion protein, a tick borne encephalitis virus or dengue fever virus E protein, a Semliki Forest virus E1 protein, a rabies virus or vesicular stomatitis virus (VSV) G protein, a baculovirus gp64, and fragments thereof.
3. The VLP of claim 1 , wherein the fusogenic protein is an envelope glycoprotein or fragment thereof.
4. The VLP of claim 3 , wherein the envelope glycoprotein is from a RNA virus or a retrovirus.
5. The VLP of claim 2 , wherein the fusogenic protein is a VSV-G glycoprotein.
6. The VLP of claim 5 , wherein the VSV-G glycoprotein comprises an alteration.
7. The VLP of claim 6 , wherein the alteration is a substitution at the second amino acid of (phenylalanine (F)) for cysteine (C) of the mature VSV-G protein.
8. VLP comprising: a first Gag fusion protein, wherein the first Gag fusion protein comprises a matrix protein, a capsid protein, a nucleocapsid protein, covalently linked to a protein of interest selected from the group consisting of a cytotoxic enzyme, an interferon, a tumor suppressor, a recombinase, a hormone, and a stem cell transcription factor; and wherein the first Gag fusion protein does not comprise a reverse transcriptase, a protease, or an integrase; a second Gag fusion protein, wherein the second Gag fusion protein comprises a protease; and a VSV-G glycoprotein.
9. An isolated nucleic acid encoding the VLP of claim 8 .
10. A method for producing the VLP of claim 1 , wherein the method comprises the steps of:
contacting a target cell with a plasmid comprising a nucleic acid encoding the Gag fusion protein of claim 1 ; and
contacting the target cell with a plasmid comprising a nucleic acid encoding a fusogenic protein having reduced ligand-binding activity.
11. The method of claim 10 , wherein the method further comprises purifying the VLP.
12. A method of treating a disease or a disorder in a subject, comprising administering to the subject the VLP of claim 1 .
13. The method of claim 12 , wherein the disease or disorder is selected from the group consisting of: cancer, metabolic diseases, inflammatory diseases, cardiovascular diseases, aging diseases, and diseases of abnormal cell proliferation.
14. A kit comprising the VLP of claim 1 .
15. The kit of claim 14 , wherein the kit further comprises instructions for using the VLP to treat a disease or disorder in a subject.
16. A kit comprising the isolated nucleic acid of claim 9 .
17. The kit of claim 16 , wherein the kit further comprises a host cell line.
18. The kit of claim 14 , wherein the kit further comprises instructions for making a VLP.
19. A virus-like particle (VLP) comprising
a Gag fusion protein, wherein the Gag fusion protein comprises a matrix protein, a capsid protein, a nucleocapsid protein, covalently linked to a protein of interest, and
a fusogenic protein having reduced ligand-binding activity,
wherein the protein of interest is selected from the group consisting of a cytotoxic enzyme, an interferon, a tumor suppressor, a protease, a recombinase, a hormone, and a stem cell transcription factor.